Patent Grant
11426466
The instant application contains a Sequence Listing in the form of a “paper copy” (PDF File) and a file containing the referenced sequences (SEQ ID NO: 1-SEQ ID NO: 221) in computer readable form (ST25 format text file) which is submitted herein. The Sequence Listing is shown using standard three letter code for amino acids, as defined in 37 C.F.R. 1.822. Said ASCII copy, created on Mar. 8, 2019, is named 40566-711_601_SL.txt and is 350,816 bytes in size.
The gut epithelium has thwarted efforts to orally administer large molecule biologics because proteins cannot diffuse across the barrier or sneak through the tight junctions. When they are taken up by endocytosis—the only route left to them—they are typically degraded in lysosomes rather than being transported into the body. This inability to be readily absorbed across the intestinal epithelium continues to be a limiting factor in developing commercially viable oral formulations of these agents. The most common solution is to use systemic administration, but that can often create considerable side effects and reduce patient convenience that negatively affects compliance.
All references disclosed herein are hereby incorporated by reference in their entirety for all purposes.
The present disclosure provides methods and composition for transport and/or delivery of a cargo molecule to certain location(s) within a cell (e.g., a supranuclear location) or across a cell (e.g., epithelial cell), either in vitro or in vivo (e.g., in a rodent or a human). Such cargo can be directed to a set of location(s) by coupling it to a carrier molecule. Such carrier molecule can interact with unique receptors both on the cell surface and intracellularly for the targeted delivery of the cargo. Various such carrier, cargos, and uses thereof are described herein.
The disclosure provides an isolated delivery construct that can comprise: a carrier derived from a domain I of an exotoxin and lacking a domain II, a domain Ib and a domain III of the exotoxin; coupled to a heterologous cargo. The carrier can consist essentially of the domain I of the exotoxin. The delivery construct can deliver the heterologous cargo according to one or more of the following: across an epithelial cell via transcytosis; to the basal side of the epithelial cell; to a supranuclear region within the epithelial cell; or to the interior of the epithelial cell via endocytosis. In some aspects, the carrier is configured to deliver a heterologous cargo to the basal side of an epithelial cell.
The disclosure provides an isolated delivery construct that can comprise: a chimeric carrier comprising an intracellular epithelial targeting domain; coupled to a heterologous cargo.
The disclosure provides an isolated delivery construct that can comprise: a chimeric carrier comprising a supranuclear epithelial targeting domain; coupled to the heterologous cargo.
The disclosure provides an isolated delivery construct that can comprise: a carrier coupled to a heterologous cargo, wherein the carrier interacts with one or more of ribophilin 1, SEC24, CK-8, TMEM132, GRP75, ERGIC-53, or perlecan, and does not display interaction with one or more of a clathrin or GPR78, or a combination thereof. The interaction can be a selective interaction. The interaction can be a pH-dependent interaction. The interaction of the carrier with the one or more of ribophilin 1, SEC24, CK-8, TMEM132, GRP75, ERGIC-53, or perlecan can occur on a surface of the epithelial cell, in the interior of an epithelial cell, or a combination thereof. The delivery of the heterologous cargo across the epithelial cell can occur in vitro from the apical surface of the epithelial cell to a basolateral compartment. The delivery of the heterologous cargo can occur in vitro from the apical surface of the epithelial cell to the interior of the epithelial cell. The delivery of the heterologous cargo can occur in vitro from the apical surface of the epithelial cell to the supranuclear region within the epithelial cell. The interaction of the carrier with the one or more of ribophilin 1, SEC24, CK-8, TMEM132, GRP75, ERGIC-53, or perlecan, or the combination thereof can occur in vitro on the apical surface of the epithelial cell, in the interior of the epithelial cell, or a combination thereof. The epithelial cell can be a polarized epithelial cell. The polarized epithelial cell can be part of a monolayer of polarized epithelial cells. The polarized epithelial cell can be from a rodent or a human. The polarized epithelial cell can be from a human. The human polarized epithelial cell can be a human polarized gut epithelial cell. The human polarized gut epithelial cell can be a Caco-2 cell. The delivery of the heterologous cargo across the epithelial cell can occur in vivo from a gut of a subject to a basolateral compartment of a subject. The delivery of the heterologous cargo can occur in vivo from a gut of a subject to the interior of the epithelial cell of a subject. The delivery of the heterologous cargo can occur in vivo from a gut of a subject to the supranuclear region within the epithelial cell of a subject. The interaction of the carrier with the one or more of ribophilin 1, SEC24, CK-8, TMEM132, GRP75, ERGIC-53, and perlecan, or the combination thereof, can occur in vivo on the apical surface of the epithelial cell of a subject, in the interior of the epithelial cell of the subject, or a combination thereof. The subject can be a rodent or a human. The subject can be a human and affected by one or more of the following: inflammatory bowel disease, psoriasis, bacterial sepsis, systemic lupus erythematosus (SLE), pemphigus vulgaris, myasthenia gravis, hemolytic anemia, thrombocytopenia purpura, Grave's disease, Sjogren's disease, dermatomyositis, Hashimoto's disease, polymyositis, inflammatory bowel disease, multiple sclerosis (MS), diabetes mellitus, rheumatoid arthritis, scleroderma, non-Hodgkin's lymphomas, Hodgkin's lymphoma, chronic lymphocytic leukemia, hairy cell leukemia, acute lymphoblastic leukemia, multiple myeloma, carcinomas of the bladder, kidney ovary, cervix, breast, lung, nasopharynx, malignant melanoma, rituximab resistant NHL or leukemia, diabetes, obesity, diabetes as a consequence of obesity, hyperglycemia, dyslipidemia, hypertriglyceridemia, syndrome X, insulin resistance, impaired glucose tolerance (IGT), diabetic dyslipidemia, hyperlipidemia, growth hormone deficiency (GHD), Turner syndrome (TS), Noonan syndrome, Prader-Willi syndrome, short stature homeobox-containing gene (SHOX) deficiency, chronic renal insufficiency, or idiopathic short stature short bowel syndrome. The epithelial cell can be a polarized epithelial cell. The polarized epithelial cell can be a polarized gut epithelial cell. The carrier can be a small molecule, a polypeptide, an aptamer, or a combination thereof. The carrier can be a small molecule. The carrier can be a polypeptide. The polypeptide can be an antibody or a functional fragment thereof. The carrier can be an aptamer. The carrier can be derived from an exotoxin. The carrier can be derived from a domain I of the exotoxin and lacks a domain II, a domain Ib and a domain III of the exotoxin The carrier that can be derived from a domain I of an exotoxin comprises an amino acid sequence that has at least 80% sequence identity to the amino acid sequence of the domain I of the exotoxin, or at least 80% sequence identity to a functional fragment thereof, wherein the exotoxin is a Cholix toxin or a Pseudomonas exotoxin A. In some aspects, the carrier comprises at least 110 amino acid residues of the domain I of the exotoxin. In some aspects, the carrier comprises at least 50 contiguous amino acid residues of the domain I of the exotoxin. The carrier that lacks the domain II, the domain Ib and the domain III of the exotoxin can comprise a portion of the domain II, the domain Ib or the domain III of the exotoxin, or a combination thereof. The portion can comprise no more than 70% of the amino acid residues of the domain II, the domain Ib or the domain III of the exotoxin. The exotoxin can be a Cholix toxin. The carrier can comprise: an amino acid sequence having at least 80% sequence identity to the amino acid sequence of SEQ ID NO: 4 or SEQ ID NO: 5 or at least 80% sequence identity to a functional fragment thereof, and no more than 347 contiguous amino acid residues from SEQ ID NO: 1. The carrier can comprise a deletion or mutation in one or more of the amino acid residues of the amino acid sequence set forth in SEQ ID NO: 4 or SEQ ID NO: 5. The carrier can comprise: an amino acid sequence having at least 90% sequence identity to the amino acid sequence of SEQ ID NO: 4 or SEQ ID NO: 5 or at least 90% sequence identity to a functional fragment thereof, and no more than 347 contiguous amino acid residues from SEQ ID NO: 1. The carrier can comprise: an amino acid sequence having at least 95% sequence identity to the amino acid sequence of SEQ ID NO: 4 or SEQ ID NO: 5 or at least 95% sequence identity to a functional fragment thereof, and no more than 347 contiguous amino acid residues from SEQ ID NO: 1. The carrier can comprise: an amino acid sequence having at least 99% sequence identity to the amino acid sequence of SEQ ID NO: 4 or SEQ ID NO: 5 or at least 99% sequence identity to a functional fragment thereof, and no more than 347 contiguous amino acid residues from SEQ ID NO: 1. The carrier can comprise: an amino acid sequence having 100% sequence identity to the amino acid sequence of SEQ ID NO: 4 or SEQ ID NO: 5 or 100% sequence identity to a functional fragment thereof, and no more than 347 contiguous amino acid residues from SEQ ID NO: 1. The carrier can comprise the amino acid sequence set forth in SEQ ID NO: 4 or SEQ ID NO: 5 or a functional fragment thereof. The carrier can comprise the amino acid sequence set forth in SEQ ID NO: 6 or SEQ ID NO: 7 or a functional fragment thereof. The carrier can comprise the amino acid sequence set forth in SEQ ID NO: 8 or SEQ ID NO: 9 or a functional fragment thereof. The carrier can comprise an amino acid sequence having at least 80% sequence identity to any one of the amino acid sequences set forth in SEQ ID NO: 148, SEQ ID NO: 149, SEQ ID NO: 150, SEQ ID NO: 151, SEQ ID NO: 152, a functional fragment thereof, or any combination thereof. The carrier can comprise a spatial structure in which one or more amino acid residues of SEQ ID NO: 148 or SEQ ID NO: 149 are in close proximity to one or more amino acid residues of SEQ ID NO: 151, and one or more amino acid residues of SEQ ID NO: 148 or SEQ ID NO: 149 are in close proximity to one or more amino acid residues of SEQ ID NO: 152. The carrier can comprise an amino acid sequence having at least 80% sequence identity to the amino acid sequence set forth in SEQ ID NO: 30 or SEQ ID NO: 31 or the amino acid sequence set forth in SEQ ID NO: 10 or SEQ ID NO: 11 or at least 80% sequence identity to a functional fragment thereof. The carrier can comprise a deletion or mutation in one or more of amino acid residues 1-187 or 1-206 of SEQ ID NO: 11 or 1-186 or 1-205 of SEQ ID NO: 10. The carrier can comprise residues 1-187 of SEQ ID NO: 30 or 1-186 of SEQ ID NO: 31 and no more than 206 contiguous amino acid residues of SEQ ID NO: 1. The carrier can comprise an amino acid sequence having at least 80% sequence identity to the amino acid sequence set forth in any one of SEQ ID NO: 10-SEQ ID NO: 31 or at least 80% sequence identity to a functional fragment thereof. The carrier can comprise the amino acid sequence set forth in SEQ ID NO: 10 or SEQ ID NO: 11 or a functional fragment thereof. The carrier can comprise an amino acid sequence having at least 80% sequence identity to the amino acid sequence set forth in SEQ ID NO: 106 or SEQ ID NO: 107 or the amino acid sequence set forth in SEQ ID NO: 30 or SEQ ID NO: 31 or at least 80% sequence identity to a functional fragment thereof. The carrier can comprise a deletion or mutation in one or more of amino acid residues 1-151 or 1-187 of SEQ ID NO: 4 or SEQ ID NO: 5. The carrier can lack any one or more of the amino acid residues 1-39 of SEQ ID NO: 5 or amino acid residues 1-38 of SEQ ID NO: 4. The carrier can comprise an amino acid sequence having at least 80% sequence identity to the amino acid sequence set forth in SEQ ID NO: 69 or SEQ ID NO: 70 or 80% sequence identity to a functional fragment thereof. The carrier can comprise residues 1-151 of SEQ ID NO: 5 or residues 1-150 of SEQ ID NO: 4 and no more than 187 contiguous amino acid residues of SEQ ID NO: 1 The carrier can comprise an amino acid sequence having at least 80% sequence identity to the amino acid sequence set forth in any one of SEQ ID NO: 30-SEQ ID NO: 107 or at least 80% sequence identity to a functional fragment thereof. The carrier can comprise the amino acid sequence set forth in SEQ ID NO: 30 or SEQ ID NO: 31 or a functional fragment thereof. The carrier can comprise an amino acid sequence having at least 80% sequence identity to the amino acid sequence set forth in SEQ ID NO: 106 or SEQ ID NO: 107 or the amino acid sequence set forth in SEQ ID NO: 124 or SEQ ID NO: 125 or at least 80% sequence identity to a functional fragment thereof. The carrier can comprise a deletion or mutation in one or more of amino acid residues 1-150 of SEQ ID NO: 6 or in one or more of amino acid residues 1-151 of SEQ ID NO: 7. The carrier can comprise residues 1-134 of SEQ ID NO: 5 or residues 1-133 of SEQ ID NO: 4 and no more than 151 contiguous amino acid residues of SEQ ID NO: 1. The carrier can comprise an amino acid sequence having at least 80% sequence identity to the amino acid sequence set forth in any of SEQ ID NO: 106-SEQ ID NO: 125 or at least 80% sequence identity to a functional fragment thereof The carrier can comprise the amino acid sequence set forth in SEQ ID NO: 106 or SEQ ID NO: 107 or a functional fragment thereof. The carrier or isolated delivery construct can comprise at least one but no more than 20 beta strands. The exotoxin can be a Pseudomonas exotoxin A. The carrier can comprise an amino acid sequence having at least 80% identity to the amino acid sequence of SEQ ID NO: 137 or at least 80% identity to a functional fragment thereof. The carrier can comprise a deletion or mutation in one or more of amino acid residues 1-252 of SEQ ID NO: 137. The carrier can comprise an amino acid sequence having at least 90% sequence identity to the amino acid sequence of 1-252 of SEQ ID NO: 137 or at least 90% sequence identity to a functional fragment thereof. The carrier can comprise an amino acid sequence having at least 95% sequence identity to the amino acid sequence of 1-252 of SEQ ID NO: 137 or at least 95% sequence identity to a functional fragment thereof. The carrier can comprise an amino acid sequence having at least 99% sequence identity to the amino acid sequence of 1-252 of SEQ ID NO: 137 or at least 99% sequence identity to a functional fragment thereof. The carrier can comprise an amino acid sequence having 100% sequence identity to the amino acid sequence of 1-252 of SEQ ID NO: 137 or 100% sequence identity to a functional fragment thereof. The carrier can comprise no more than 252 contiguous amino acid residues from SEQ ID NO: 134. In some aspects, the carrier comprises residues 1-252 of SEQ ID NO: 134. The carrier can comprise at least one N-terminal methionine residue. The carrier can comprise an amino acid sequence having at least 80% sequence identity to an amino acid sequence set forth in any one of SEQ ID NO: 5, SEQ ID NO: 7, SEQ ID NO: 9, SEQ ID NO: 11, SEQ ID NO: 31, SEQ ID NO: 107, SEQ ID NO: 125, or 80% sequence identity to a functional fragment thereof. The delivery construct can form a multimer. The multimer can be formed by multimerization of the heterologous cargo. The multimer can be a heteromer or a homomer The homomer can be a homodimer. The homodimer can be formed by dimerization of the heterologous cargo.
The present disclosure provides an isolated delivery construct that can comprise: a carrier comprising a first portion and a second portion, wherein the first portion is derived from a first exotoxin and the second portion is derived from a second exotoxin; coupled to a heterologous cargo. The first exotoxin can be Cholix. The second exotoxin can be PE. The first portion can be derived from a domain I, a domain II, a domain Ib, or a domain III of Cholix, or any combination thereof. The first portion can comprise an amino acid sequence having at least 80% sequence identity to any one of the amino acid sequences set forth in SEQ ID NO: 1-SEQ ID NO: 125 or SEQ ID NO: 133, a functional fragment thereof, or any combination thereof. The first portion can comprise an amino acid sequence having at least 80% sequence identity to any one of the amino acid sequences set forth in SEQ ID NO: 148-SEQ ID NO: 152, a functional fragment thereof, or any combination thereof. The first portion can comprise an amino acid sequence having at least 80% sequence identity to any one of the amino acid sequences set forth in SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 10, or SEQ ID NO: 11, a functional fragment thereof, or any combination thereof. The second portion can be derived from a domain I, a domain II, a domain Ib, or a domain III of PE, or any combination thereof. The second portion can comprise an amino acid sequence having at least 80% sequence identity to any one of the amino acid sequences set forth in SEQ ID NO: 137-SEQ ID NO: 145, a functional fragment thereof, or any combination thereof. The first portion can be chemically coupled or recombinantly coupled to the second portion. The first portion can be directly or indirectly coupled to the second portion. The carrier can comprise an amino acid sequence having at least 80% sequence identity to the amino acid sequence SEQ ID NO: 146 or SEQ ID NO: 147. The carrier can be chemically coupled or recombinantly coupled to the heterologous cargo. The carrier can be covalently coupled to the heterologous cargo. The heterologous cargo can be coupled to the C-terminus of the carrier. The heterologous cargo can be coupled to the N-terminus of the carrier. The carrier can be coupled directly to the heterologous cargo. The carrier can be coupled indirectly to the heterologous cargo. The carrier can be coupled to the heterologous cargo via a spacer. The spacer can comprise an amino acid spacer. The amino acid spacer can be between 1 and 50 amino acid residues in length. The amino acid spacer can comprise one or more glycine residues and one or more serine residues. The spacer can be a cleavable spacer. The cleavable spacer can comprise an amino acid sequence set forth in any one of SEQ ID NO: 174-SEQ ID NO: 206. The spacer can be a non-cleavable spacer. The non-cleavable spacer can comprise one or more of the amino acid sequences GTGGS (SEQ ID NO: 207), GGGGS (SEQ ID NO: 208), GGGGSGGGGS (SEQ ID NO: 209), GGGGSGGGGSGGGGS (SEQ ID NO: 210), or GGGGSGGG (SEQ ID NO: 211). The non-cleavable spacer can comprise one or more of (GGGGS)x (SEQ ID NO: 212), wherein x=1, 2, 3, 4, 5, 6, 7, 8, 9, or 10. The non-cleavable spacer can comprise one or more of (GS)x (SEQ ID NO: 213), wherein x=1, 2, 3, 4, 5, 6, 7, 8, 9, or 10. The spacer can comprise one or more fragments of the domain II, the domain Ib or the domain III of the exotoxin, or a combination thereof. The spacer can comprise at most 80 amino acid residues of the domain II, 80 amino acid residues of the domain III, or a combination thereof. The heterologous cargo can be a macromolecule, a small molecule, a polypeptide, a nucleic acid, a mRNA, a miRNA, a shRNA, a siRNA, an antisense molecule, an antibody, a DNA, a plasmid, a vaccine, a polymer a nanoparticle, or a catalytically-active material. The heterologous cargo can be a biologically active cargo. The biologically active cargo can be a cytokine, a hormone, a therapeutic antibody, a functional fragment thereof, or any combination thereof. The cytokine can be IL-1, IL-2, IL-3, IL-4, IL-5, IL-6, IL-7, IL-8, IL-9, IL-10, IL-11, IL-12, IL-13, IL-14, IL-15, IL-16, IL-17, IL-18, IL-19, IL-20, IL-21, IL-22, IL-23, IL-24, IL-25, IL-26, IL-27, IL-28, IL-29, or IL-30. The cytokine can have the amino acid sequence set forth in SEQ ID NO: 217 or SEQ ID NO: 218. The hormone can have the amino acid sequence set forth in SEQ ID NO: 215 or SEQ ID NO: 216. The therapeutic antibody can be an anti-TNFa antibody. The anti-TNFa antibody can be adalimumab or infliximab. The heterologous cargo can be a detectable agent. The detectable agent can be a fluorophore, a contrast agent, an X-ray contrast agent, a PET agent, a nanoparticle, or a radioisotope. The fluorophore can be a red fluorescent protein (RFP). The RFP can have the amino acid sequence set forth in SEQ ID NO: 220.
A delivery construct of the present disclosure can comprise an amino acid sequence having at least 80% sequence identity to the amino acid sequence set forth in any one of SEQ ID NO: 155, SEQ ID NO: 156, or SEQ ID NO: 158-SEQ ID NO: 165, or at least 80% sequence identity to a functional fragment thereof. A delivery construct of the present disclosure can comprise an amino acid sequence having at least 90% sequence identity to the amino acid sequence set forth in any one of SEQ ID NO: 155, SEQ ID NO: 156, or SEQ ID NO: 158-SEQ ID NO: 165, or at least 90% sequence identity to a functional fragment thereof. A delivery construct of the present disclosure can comprise an amino acid sequence having at least 95% sequence identity to the amino acid sequence set forth in any one of SEQ ID NO: 155, SEQ ID NO: 156, or SEQ ID NO: 158-SEQ ID NO: 165, or at least 95% sequence identity to a functional fragment thereof. A delivery construct of the present disclosure can comprise an amino acid sequence having at least 99% sequence identity to the amino acid sequence set forth in any one of SEQ ID NO: 155, SEQ ID NO: 156, or SEQ ID NO: 158-SEQ ID NO: 165, or at least 99% sequence identity to a functional fragment thereof. A delivery construct of the present disclosure can comprise an amino acid sequence having 100% sequence identity to the amino acid sequence set forth in any one of SEQ ID NO: 155, SEQ ID NO: 156, or SEQ ID NO: 158-SEQ ID NO: 165, or 100% sequence identity to a functional fragment thereof.
The present disclosure provides a pharmaceutical composition comprising: an isolated delivery construct as described herein; and a pharmaceutically acceptable carrier. The composition can be formulated for oral administration, topical administration, pulmonary administration, intra-nasal administration, buccal administration, sublingual administration or ocular administration. The composition can be formulated for oral administration. The composition can be formulated in a capsule or tablet.
The present disclosure provides a polynucleotide that can encode an isolated delivery construct as described herein.
In various aspects, the present disclosure provides a vector comprising a polynucleotide encoding an isolated delivery construct as described herein.
The present disclosure provides a host cell that can comprise a vector that expresses a delivery construct, wherein the host cell comprises a vector comprising a polynucleotide encoding an isolated delivery construct as described herein.
The present disclosure provides a method of delivering a heterologous cargo across an epithelial cell, the method can comprise: applying a delivery construct to the apical surface of the epithelial cell; and delivering the delivery construct to the basal side of the epithelial cell at a rate greater than 10−6 cm/sec, wherein the delivery construct comprises: a carrier; coupled to the heterologous cargo. In some aspects, the method further comprises releasing the delivery construct from the basal side of the epithelial cell following delivery across the epithelial cell. In some aspects, the carrier is configured to deliver a heterologous cargo to the basal side of an epithelial cell.
The present disclosure provides a method of delivering a heterologous cargo to the interior of an epithelial cell via endocytosis, the method can comprise: applying a delivery construct to the apical surface of the epithelial cell; and delivering the delivery construct to the interior of the epithelial cell via endocytosis, wherein the delivery construct comprises: a carrier; coupled to the heterologous cargo.
The present disclosure provides a method of delivering a heterologous cargo to a supranuclear region within an epithelial cell via endocytosis, the method can comprise: applying a delivery construct to the apical surface of an epithelial cell; and delivering the delivery construct to the supranuclear region within the epithelial cell via endocytosis, wherein the delivery construct comprises: a carrier; coupled to the heterologous cargo.
The present disclosure provides a method of interacting with ribophilin 1, SEC24, CK-8, TMEM132, GRP75, ERGIC-53, or perlecan, or a combination thereof, the method can comprise: applying a delivery construct to the apical surface of the epithelial cell; and interacting the delivery construct with the ribophilin 1, SEC24, CK-8, TMEM132, GRP75, ERGIC-53, or perlecan, or the combination thereof, wherein the delivery construct comprises: a carrier; coupled to a heterologous cargo. The carrier can interact with one or more of ribophilin 1, SEC24, CK-8, TMEM132, GRP75, ERGIC-53, or perlecan, or the combination thereof, and does not display interaction with one or more of a clathrin or GPR78, or a combination thereof. The interaction can be a selective interaction or a pH-dependent interaction, or a combination thereof. The interaction of the carrier with the one or more of ribophilin 1, SEC24, CK-8, TMEM132, GRP75, ERGIC-53, or perlecan can occur on a surface of an epithelial cell, in the interior of an epithelial cell, or a combination thereof.
The present disclosure provides a method of treating a disease in a subject in need thereof, the method can comprise administering to the subject a delivery construct comprising: a carrier; coupled to a heterologous cargo; wherein the delivery construct is capable of delivering the heterologous cargo to the interior of an epithelial cell.
The present disclosure provides a method of treating a disease in a subject in need thereof, the method can comprise administering to the subject a delivery construct comprising: a carrier; coupled to a heterologous cargo; wherein the delivery construct is capable of delivering the heterologous cargo to a supranuclear region within an epithelial cell.
The present disclosure provides a method of diagnosing a disease in a subject in need thereof, the method can comprise administering to the subject a delivery construct comprising: a carrier; coupled to a heterologous cargo; wherein the delivery construct is capable of delivering the heterologous cargo to the interior of an epithelial cell.
The present disclosure provides a method of diagnosing a disease in a subject in need thereof, the method can comprise administering to the subject a delivery construct comprising: a carrier; coupled to a heterologous cargo; wherein the delivery construct is capable of delivering the heterologous cargo to a supranuclear region within an epithelial cell.
The present disclosure provides a method of treating a disease in a subject in need thereof, the method can comprise administering to the subject a delivery construct comprising: a carrier derived from a domain I of an exotoxin and lacking a domain II, a domain Ib and a domain III of the exotoxin; coupled to a heterologous cargo; wherein the delivery construct is capable of delivering the heterologous cargo via transcytosis across an epithelial cell.
The present disclosure provides a method of diagnosing a disease in a subject in need thereof, the method can comprise administering to the subject a delivery construct comprising: a carrier derived from a domain I of an exotoxin and lacking a domain II, a domain Ib and a domain III of the exotoxin; coupled to a heterologous cargo; wherein the delivery construct is capable of delivering the heterologous cargo via transcytosis across an epithelial cell. The delivery of the heterologous cargo across the epithelial cell can occur in vitro from the apical surface of the epithelial cell to a basolateral compartment. The delivery of the heterologous cargo can occur in vitro from the apical surface of the epithelial cell to the interior of the epithelial cell. The delivery of the heterologous cargo can occur in vitro from the apical surface of the epithelial cell to the supranuclear region within the epithelial cell. The interaction of the carrier with the one or more of ribophilin 1, SEC24, CK-8, TMEM132, GRP75, ERGIC-53, or perlecan, or the combination thereof, can occur in vitro on the apical surface of the epithelial cell, in the interior of the epithelial cell, or a combination thereof. The epithelial cell can be a polarized epithelial cell. The polarized epithelial cell can be part of a monolayer of polarized epithelial cells. The polarized epithelial cell can be from a rodent. The polarized epithelial cell can be from a human. The human polarized epithelial cell can be a human polarized gut epithelial cell. The human polarized gut epithelial cell can be a Caco-2 cell. The delivery of the heterologous cargo across the epithelial cell can occur in vivo from a gut of a subject to a basolateral compartment of the subject. The delivery of the heterologous cargo can occur in vivo from a gut of a subject to the interior of the epithelial cell of the subject. The delivery of the heterologous cargo can occur in vivo from a gut of a subject to the supranuclear region within the epithelial cell of the subject. The interaction of the carrier with the one or more of ribophilin 1, SEC24, CK-8, TMEM132, GRP75, ERGIC-53, and perlecan, or the combination thereof, can occur in vivo on the apical surface of the epithelial cell of a subject, in the interior of the epithelial cell of the subject, or a combination thereof. The subject can be a rodent or a human. The epithelial cell can be a polarized epithelial cell. The polarized epithelial cell can be a polarized gut epithelial cell. The method further can comprise formulating the delivery construct for administration to the subject. The formulation can comprise one or more pharmaceutically acceptable carriers. The delivery construct can be formulated for oral administration, topical administration, pulmonary administration, intra-nasal administration, buccal administration, sublingual administration or ocular administration. The composition can be formulated for oral administration. The disease can be an inflammatory disease, an autoimmune disease, a cancer, a metabolic disease, a fatty liver disease, or a growth hormone deficient growth disorder. The inflammatory disease can be an inflammatory bowel disease, psoriasis or bacterial sepsis. The inflammatory bowel disease can be Crohn's disease, ulcerative colitis, collagenous colitis, lymphocytic colitis, ischemic colitis, diversion colitis, Behcet's syndrome or indeterminate colitis. The autoimmune disease can be systemic lupus erythematosus (SLE), pemphigus vulgaris, myasthenia gravis, hemolytic anemia, thrombocytopenia purpura, Grave's disease, Sjogren's disease, dermatomyositis, Hashimoto's disease, polymyositis, inflammatory bowel disease, multiple sclerosis (MS), diabetes mellitus, rheumatoid arthritis, or scleroderma. The cancer can be a non-Hodgkin's lymphoma, Hodgkin's lymphoma, chronic lymphocytic leukemia, hairy cell leukemia, acute lymphoblastic leukemia, multiple myeloma, carcinomas of the bladder, kidney ovary, cervix, breast, lung, nasopharynx, malignant melanoma, rituximab resistant NHL, or leukemia. The metabolic disease can be diabetes, obesity, diabetes as a consequence of obesity, hyperglycemia, dyslipidemia, hypertriglyceridemia, syndrome X, insulin resistance, impaired glucose tolerance (IGT), diabetic dyslipidemia, or hyperlipidemia. The carrier can be a small molecule. The carrier can be a polypeptide. The polypeptide can be an antibody or a functional fragment thereof. The carrier can be an aptamer. The carrier can be derived from an exotoxin. The carrier can be derived from a domain I of the exotoxin and lacks a domain II, a domain Ib and a domain III of the exotoxin. The carrier can be derived from a domain I of an exotoxin comprises an amino acid sequence that has at least 80% sequence identity to the amino acid sequence of the domain I of the exotoxin, or at least 80% sequence identity to a functional fragment thereof, wherein the exotoxin is a Cholix toxin or a Pseudomonas exotoxin A. The carrier can comprise at least 130 amino acid residues of the domain I of the exotoxin. The carrier can comprise at least 150 contiguous amino acid residues of the domain I of the exotoxin. The carrier that lacks the domain II and domain III of the exotoxin can comprise a portion of the domain II or the domain III of the exotoxin, or a combination thereof. The portion comprises no more than 82 of the amino acid residues of the domain II or the domain III of the exotoxin. The exotoxin can be a Cholix toxin. The carrier can comprise: an amino acid sequence having at least 80% sequence identity to the amino acid sequence of SEQ ID NO: 4 or SEQ ID NO: 5 or at least 80% sequence identity to a functional fragment thereof, and no more than 347 contiguous amino acid residues from SEQ ID NO: 1. The carrier can comprise a deletion or mutation in one or more of amino acid residues of the amino acid sequence set forth in SEQ ID NO: 4 or SEQ ID NO: 5. The carrier can comprise: an amino acid sequence having at least 90% sequence identity to the amino acid sequence of SEQ ID NO: 4 or SEQ ID NO: 5 or at least 90% sequence identity to a functional fragment thereof, and no more than 347 contiguous amino acid residues from SEQ ID NO: 1. The carrier can comprise: an amino acid sequence having at least 95% sequence identity to the amino acid sequence of SEQ ID NO: 4 or SEQ ID NO: 5 or at least 95% sequence identity to a functional fragment thereof, and no more than 347 contiguous amino acid residues from SEQ ID NO: 1. The carrier can comprise: an amino acid sequence having at least 99% sequence identity to the amino acid sequence of SEQ ID NO: 4 or SEQ ID NO: 5 or at least 99% sequence identity to a functional fragment thereof, and no more than 347 contiguous amino acid residues from SEQ ID NO: 1. The carrier can comprise: an amino acid sequence having 100% sequence identity to the amino acid sequence of SEQ ID NO: 4 or SEQ ID NO: 5 or 100% sequence identity to a functional fragment thereof, and no more than 347 contiguous amino acid residues from SEQ ID NO: 1. The carrier can comprise the amino acid sequence set forth in SEQ ID NO: 4 or SEQ ID NO: 5 or a functional fragment thereof. In some aspects, the carrier comprises the amino acid sequence set forth in SEQ ID NO: 6 or SEQ ID NO: 7 or a functional fragment thereof. The carrier can comprise the amino acid sequence set forth in SEQ ID NO: 8 or SEQ ID NO: 9 or a functional fragment thereof. The carrier can comprise an amino acid sequence having at least 80% sequence identity to any one of the amino acid sequences set forth in SEQ ID NO: 148, SEQ ID NO: 149, SEQ ID NO: 150, SEQ ID NO: 151, SEQ ID NO: 152, a functional fragment thereof, or any combination thereof. The carrier can comprise an amino acid sequence having at least 80% sequence identity to the amino acid sequence set forth in SEQ ID NO: 30 or SEQ ID NO: 31 or the amino acid sequence set forth in SEQ ID NO: 10 or SEQ ID NO: 11 or at least 80% sequence identity to a functional fragment thereof. The carrier can comprise a deletion or mutation in one or more of amino acid residues 1-187 or 1-206 of SEQ ID NO: 5 or one or more of amino acid residues 1-186 or 1-205 of SEQ ID NO: 4. The carrier can comprise residues 1-187 of SEQ ID NO: 5 or residues 1-186 of SEQ ID NO: 4 and no more than 206 contiguous amino acid residues of SEQ ID NO: 1. The carrier can comprise an amino acid sequence having at least 80% sequence identity to the amino acid sequence set forth in any one of SEQ ID NO: 1-SEQ ID NO: 31 or at least 80% sequence identity to a functional fragment thereof. The carrier can comprise the amino acid sequence set forth in SEQ ID NO: 10 or SEQ ID NO: 11 or a functional fragment thereof. The carrier can comprise an amino acid sequence having at least 80% sequence identity to the amino acid sequence set forth in SEQ ID NO: 106 or SEQ ID NO: 107 or the amino acid sequence set forth in SEQ ID NO: 30 or SEQ ID NO: 31 or at least 80% sequence identity to a functional fragment thereof. The carrier can comprise a deletion or mutation in one or more of amino acid residues 1-151 or 1-187 of SEQ ID NO: 5 or in one or more of amino acid residues 1-150 or 1-186 of SEQ ID NO: 4. The carrier can lack any one or more of the amino acid residues 1-39 of SEQ ID NO: 5 or residues 1-38 of SEQ ID NO: 4. The carrier can comprise an amino acid sequence having at least 80% sequence identity to the amino acid sequence set forth in SEQ ID NO: 69 or SEQ ID NO: 70 or 80% sequence identity to a functional fragment thereof. The carrier can comprise residues 1-151 of SEQ ID NO: 5 or residues 1-150 of SEQ ID NO: 4 and no more than 187 contiguous amino acid residues of SEQ ID NO: 1. The carrier can comprise an amino acid sequence having at least 80% sequence identity to the amino acid sequence set forth in any of SEQ ID NO: 30-SEQ ID NO: 107 or at least 80% sequence identity to a functional fragment thereof. The carrier can comprise the amino acid sequence set forth in SEQ ID NO: 30 or SEQ ID NO: 31 or a functional fragment thereof. The carrier can comprise an amino acid sequence having at least 80% sequence identity to the amino acid sequence set forth in SEQ ID NO: 124 or SEQ ID NO: 125 or the amino acid sequence set forth in SEQ ID NO: 106 or SEQ ID NO: 107 or at least 80% sequence identity to a functional fragment thereof. The carrier can comprise a deletion or mutation in one or more of amino acid residues 1-151 of SEQ ID NO: 5 or in one or more of amino acid residues 1-150 of SEQ ID NO: 4. The carrier can comprise residues 1-134 of SEQ ID NO: 5 or residues 1-133 of SEQ ID NO: 4 and no more than 151 contiguous amino acid residues of SEQ ID NO: 1. The carrier can comprise an amino acid sequence having at least 80% sequence identity to the amino acid sequence set forth in any one of SEQ ID NO: 106-SEQ ID NO: 125 or at least 80% sequence identity to a functional fragment thereof. The carrier can comprise the amino acid sequence set forth in SEQ ID NO: 106 or SEQ ID NO: 107 or a functional fragment thereof. The carrier can comprise at least one but no more than 20 beta strands. The exotoxin can be a Pseudomonas exotoxin A. The carrier can comprise an amino acid sequence having at least 80% identity to the amino acid sequence of SEQ ID NO: 137 or at least 80% identity to a functional fragment thereof. The carrier can comprise a deletion or mutation in one or more of amino acid residues 1-252 of SEQ ID NO: 137. The carrier can comprise an amino acid sequence having at least 90% sequence identity to the amino acid sequence of 1-252 of SEQ ID NO: 137 or at least 90% sequence identity to a functional fragment thereof. The carrier can comprise an amino acid sequence having at least 95% sequence identity to the amino acid sequence of 1-252 of SEQ ID NO: 137 or at least 95% sequence identity to a functional fragment thereof. The carrier can comprise an amino acid sequence having at least 99% sequence identity to the amino acid sequence of 1-252 of SEQ ID NO: 137 or at least 99% sequence identity to a functional fragment thereof. The carrier can comprise an amino acid sequence having 100% sequence identity to the amino acid sequence of 1-252 of SEQ ID NO: 137 or 100% sequence identity to a functional fragment thereof. The carrier can comprise residues 1-252 of SEQ ID NO: 135. The carrier can comprise a first portion and a second portion, wherein the first portion is derived from a first exotoxin and the second portion is derived from a second exotoxin. The first exotoxin can be Cholix and the second exotoxin can be PE. The first portion can be derived from a domain I, a domain II, a domain Ib, or a domain III of Cholix, or any combination thereof. The first portion can comprise an amino acid sequence having at least 80% sequence identity to any one of the amino acid sequences set forth in SEQ ID NO: 1-SEQ ID NO: 125, a functional fragment thereof, or any combination thereof. The first portion can comprise an amino acid sequence having at least 80% sequence identity to any one of the amino acid sequences set forth in SEQ ID NO: 148-SEQ ID NO: 152, a functional fragment thereof, or any combination thereof. The first portion can comprise an amino acid sequence having at least 80% sequence identity to any one of the amino acid sequences set forth in SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 10, or SEQ ID NO: 11, a functional fragment thereof, or any combination thereof. The second portion can be derived from a domain I, a domain II, a domain Ib, or a domain III of PE, or any combination thereof. The second portion can comprise an amino acid sequence having at least 80% sequence identity to any one of the amino acid sequences set forth in SEQ ID NO: 137-SEQ ID NO: 145, a functional fragment thereof, or any combination thereof. The first portion can be chemically coupled or recombinantly coupled to the second portion. The first portion can be directly or indirectly coupled to the second portion. The carrier can comprise an amino acid sequence having at least 80% sequence identity to the amino acid sequence SEQ ID NO: 146 or SEQ ID NO: 147. The carrier can further comprise at least one N-terminal methionine residue. The carrier can comprise an amino acid sequence having at least 80% sequence identity to an amino acid sequence set forth in any one of SEQ ID NO: 5, SEQ ID NO: 7, SEQ ID NO: 9, SEQ ID NO: 11, SEQ ID NO: 31, SEQ ID NO: 107, SEQ ID NO: 125, or 80% sequence identity to a functional fragment thereof. The delivery construct can form a multimer. The multimer can be formed by multimerization of the heterologous cargo. The multimer can be a heteromer or a homomer. The homomer can be a homodimer. The homodimer can be formed by dimerization of the heterologous cargo. The carrier can be chemically coupled or recombinantly coupled to the heterologous cargo. The carrier can be covalently coupled to the heterologous cargo. The heterologous cargo can be coupled to the C-terminus of the carrier. The heterologous cargo can be coupled to the N-terminus of the carrier. The carrier can be coupled directly to the heterologous cargo. The carrier can be coupled indirectly to the heterologous cargo. The carrier can be coupled to the heterologous cargo via a spacer. The spacer can comprise an amino acid spacer. The amino acid spacer can comprise one or more glycine residues and one or more serine residues. The amino acid spacer can be between 1 and 50 amino acid residues in length. The spacer can be a cleavable spacer. The cleavable spacer can comprise an amino acid sequence selected from the group consisting of the amino acid sequences set forth in SEQ ID NO: 174-SEQ ID NO: 206. The spacer can be a non-cleavable spacer. The non-cleavable spacer can comprise one or more of the amino acid sequences GTGGS (SEQ ID NO: 207), GGGGS (SEQ ID NO: 208), GGGGSGGGGS (SEQ ID NO: 209), GGGGSGGGGSGGGGS (SEQ ID NO: 210), or GGGGSGGG (SEQ ID NO: 211). The non-cleavable spacer can comprises one or more of (GGGGS)x (SEQ ID NO: 212), wherein x=1, 2, 3, 4, 5, 6, 7, 8, 9, or 10. The non-cleavable spacer can comprise one or more of (GS)x (SEQ ID NO: 213), wherein x=1, 2, 3, 4, 5, 6, 7, 8, 9, or 10. The spacer can comprise one or more fragments of the domain II, a domain Ib or the domain III of the exotoxin, or a combination thereof. The spacer can comprise at most 82 amino acid residues of the domain II, 82 amino acid residues of the domain III, or a combination thereof. The heterologous cargo can be a macromolecule, a small molecule, a polypeptide, a nucleic acid, a mRNA, a miRNA, a shRNA, a siRNA, an antisense molecule, an antibody, a DNA, a plasmid, a vaccine, a polymer a nanoparticle, or a catalytically-active material. The heterologous cargo can be a biologically active cargo. The biologically active cargo can be a cytokine, a hormone, a therapeutic antibody, a functional fragment thereof, or any combination thereof. The cytokine can be IL-1, IL-2, IL-3, IL-4, IL-5, IL-6, IL-7, IL-8, IL-9, IL-10, IL-11, IL-12, IL-13, IL-14, IL-15, IL-16, IL-17, IL-18, IL-19, IL-20, IL-21, IL-22, IL-23, IL-24, IL-25, IL-26, IL-27, IL-28, IL-29, or IL-30. The cytokine can have the amino acid sequence set forth in SEQ ID NO: 217 or SEQ ID NO: 218. The hormone can have the amino acid sequence set forth in SEQ ID NO: 215 or SEQ ID NO: 216. The therapeutic antibody can be an anti-TNFa antibody. The anti-TNFa antibody can be adalimumab or infliximab. The heterologous cargo can be a detectable agent. The detectable agent can be a fluorophore, a contrast agent, an X-ray contrast agent, a PET agent, a nanoparticle, or a radioisotope. The fluorophore can be a red fluorescent protein (RFP). The RFP can have the amino acid sequence set forth in SEQ ID NO: 220.
The present disclosure relates to novel non-naturally occurring delivery constructs that can comprise a bacterial toxin-derived chimeric carrier coupled to a biologically active cargo; wherein the chimeric carrier is derived from a domain I but does not comprise a domain II, a domain Ib, or a domain III of the bacterial toxin (e.g., an exotoxin); and wherein the delivery construct is capable of delivering a heterologous (e.g., a biologically active) cargo via transcytosis transport across an epithelial cell (e.g., an intestinal epithelial cell).
The carrier can be derived from a domain I of an exotoxin and is capable of recognizing and interacting with one or more receptors on the luminal (e.g., apical) surface of intestinal epithelial cells. The receptor can be selective or non-selective. In some aspects, the receptor that a carrier interacts with is a non-selective scavenger receptor or a transmembrane receptor 132 (TMEM132) receptor. Interaction of the delivery constructs with a cell surface receptor that is present on the apical membrane of a polarized epithelial cell can occur with sufficient affinity to allow endocytosis of the delivery construct. The carrier that a delivery construct of the present disclosure is comprised of can bind to receptor(s) known to be present on the apical membrane of an epithelial cell by one of skill in the art without limitation. In various embodiments, the receptor binding domain of the delivery construct can bind to low density lipoprotein receptor-related protein 1 (LRP1) or TMEM132 receptor.
A delivery construct as described herein can be capable of delivering a heterologous (e.g., a biologically active) cargo across an epithelial cell from the apical side to a basolateral compartment and/or the Lamina propria. A delivery construct as described herein can be capable of delivering a heterologous (e.g., a biologically active) cargo into an epithelial cell (e.g., a polarized gut epithelial cell), such as an intracellular vesicle or compartment or the cytosol of the epithelial cell, thereby allowing for accumulation of the heterologous (e.g., biologically active) cargo in the epithelial cell. The carrier can be derived from the domain I of an exotoxin selected from the group consisting of cholix carrier (Cholix) and Pseudomonas exotoxin A (PE).
The carrier can be a polypeptide derived from Cholix and/or PE and having: at most 5 amino acid residues; at most 10 amino acid residues; at most 15 amino acid residues; at most 20 amino acid residues; at most 30 amino acid residues; at most 40 amino acid residues; at most 50 amino acid residues; at most 60 amino acid residues; at most 70 amino acid residues; at most 80 amino acid residues; at most 90 amino acid residues; at most 100 amino acid residues; at most 110 amino acid residues; at most 120 amino acid residues; at most 130 amino acid residues; at most 140 amino acid residues; at most 150 amino acid residues; at most 160 amino acid residues; at most 170 amino acid residues; at most 180 amino acid residues; at most 190 amino acid residues; at most 200 amino acid residues; at most 210 amino acid residues; at most 220 amino acid residues; at most 230 amino acid residues; at most 240 amino acid residues; at most 250 amino acid residues; at most 260 amino acid residues; and at most 265 amino acid residues.
The carrier can be derived from a domain I of a Cholix exotoxin and can comprise an amino acid sequence selected from the group consisting of an amino acid sequence having greater than 50% homology to SEQ ID NO: 4, having greater than 60% homology to SEQ ID NO: 4, having greater than 70% homology to SEQ ID NO: 4, having greater than 80% homology to SEQ ID NO: 4, having greater than 85% homology to SEQ ID NO: 4, having greater than 90% homology to SEQ ID NO: 4, and having greater than 95% homology to SEQ ID NO: 4. In some cases, the delivery construct is derived from cholix exotoxin (Cholix) and comprises the receptor binding domain polypeptide having the amino acid sequence set forth in SEQ ID NO: 4. The carrier can comprise an amino acid sequence with greater than 90% homology to SEQ ID NO: 4. The carrier can comprise an amino acid sequence with greater than 95% homology to SEQ ID NO: 4. The carrier can comprise a receptor binding domain polypeptide wherein one or more amino residues of SEQ ID NO: 4 is substituted with another amino acid. The carrier can comprise a receptor binding domain polypeptide that is a truncated portion of the amino acid sequence set forth in SEQ ID NO: 4.
The carrier can be derived from a domain I of a Pseudomonas exotoxin A (PE) and can comprise a polypeptide having the amino acid sequence set forth in SEQ ID NO: 137. The delivery construct can comprise an amino acid sequence with greater than 90% homology to SEQ ID NO: 137. The carrier can comprise an amino acid sequence with greater than 95% homology to SEQ ID NO: 137. The carrier can comprise a receptor binding domain polypeptide wherein one or more amino residues of SEQ ID NO: 137 is substituted with another amino acid. The carrier can comprise a receptor binding domain polypeptide that is a truncated portion of the amino acid sequence set forth in SEQ ID NO: 137.
A delivery construct can comprise a carrier, wherein the carrier comprises one or more amino acid residues of one exotoxin domain I (e.g., a Cholix or PE domain I) is replaced by one or more amino acid residues of a second exotoxin domain I (e.g., a Cholix or PE domain I), (also referred to hereinafter as a hybrid or chimeric carrier). The carrier can comprise an amino acid sequence wherein one or more amino acid residues of SEQ ID NO: 4 is replaced by one or more amino acid residues of SEQ ID NO: 137. The carrier can comprise an amino acid sequence wherein one or more amino acid residues of SEQ ID NO: 137 is replaced by one or more amino acid residues of SEQ ID NO: 4. The carrier can comprise an amino acid sequence wherein amino acid residues 77-87 of SEQ ID NO: 4 are replaced by amino acid residues of a second bacterial carrier receptor binding domain polypeptide. The carrier can comprise an amino acid sequence wherein amino acid residues 188-236 of SEQ ID NO: 4 are replaced by amino acid residues of a second bacterial carrier receptor binding domain polypeptide. The carrier can comprise an amino acid sequence wherein amino acid residues 69-71 of SEQ ID NO: 137 are replaced by amino acid residues of a second bacterial carrier receptor binding domain polypeptide. The carrier can comprise an amino acid sequence wherein amino acid residues 177-228 of SEQ ID NO: 137 are replaced by amino acid residues of a second bacterial carrier receptor binding domain polypeptide.
A carrier of the present disclosure that can be derived from a domain I of an exotoxin and can further comprise a portion of a domain II, a portion of a domain Ib, and/or a portion of a domain III of the same or another exotoxin. Thus, a carrier can comprise a domain I of an exotoxin, or a truncated and/or modified version thereof, and one or more portions derived from a domain II, domain Ib, and/or domain III of the same or a different exotoxin. The domain II, or modified domain II, and domain III, or modified domain III, can be derived from the same bacterial toxin. The domain II, or modified domain II, and domain III, or modified domain III, can be derived from a bacterial carrier selected from the group consisting of cholix carrier (Cholix) and Pseudomonas exotoxin A (PE), botulinum toxin, diptheria toxin, pertussis toxin, cholera toxin, heat-labile E. coli entero-toxin, shiga toxin, and shiga-like toxin. Toxicity of the bacterial carrier (e.g., Cholix or PE) may not be required for transport across epithelial layers such as the gut epithelium. For example, a delivery construct as described herein can comprise a carrier coupled to a heterologous cargo, and wherein the carrier is derived from a Cholix domain I (e.g., having an amino acid sequence set forth in any one of SEQ ID NO: 4-SEQ ID NO: 125) and further comprising portions of a domain II (e.g., SEQ ID NO: 126 or SEQ ID NO: 138), a domain Ib (e.g., SEQ ID NO: 127 or SEQ ID NO: 139), and/or a domain III (e.g., SEQ ID NO: 128 or SEQ ID NO: 140) of an exotoxin (e.g., Cholix and/or PE).
A delivery construct can comprise a carrier having the amino acid sequence derived from the sequence set forth in SEQ ID NO: 4, a translocation domain having the amino acid sequence derived from the sequence set forth in SEQ ID NO: 126, and a non-toxic catalytic domain having the amino acid sequence derived from the sequence set forth in SEQ ID NO: 128. A delivery constructs can comprise a receptor binding domain polypeptide having the amino acid sequence derived from the sequence set forth in SEQ ID NO: 136, a translocation domain having the amino acid sequence derived from the sequence set forth in SEQ ID NO: 137, and a non-toxic catalytic domain having the amino acid sequence derived from the sequence set forth in SEQ ID NO: 139. The delivery construct can comprises the amino acid sequence set forth in SEQ ID NO: 146. In various embodiments, the delivery construct comprises the amino acid sequence set forth in SEQ ID NO: 147.
The delivery constructs of the present disclosure can comprise a carrier coupled to a heterologous cargo. The heterologous cargo can be a biologically active cargo. The heterologous cargo can be a detectable agent. The carrier can be coupled to a biologically active cargo to produce a delivery construct that is capable of delivering the biologically active cargo via transcytosis transport across an intestinal epithelium. The biologically active cargo can be selected from e.g., a macromolecule, small molecule, peptide, polypeptide, nucleic acid, mRNA, miRNA, shRNA, siRNA, antisense molecule, antibody, DNA, plasmid, vaccine, polymer nanoparticle, or catalytically-active material. The biologically active cargo can be an enzyme selected from hyaluronidase, streptokinase, tissue plasminogen activator, urokinase, or PGE-adenosine deaminase. The biologically active cargo can comprises an amino acid sequence selected from the group consisting of the amino acid sequences set forth in SEQ ID NO: 214, SEQ ID NO: 215, SEQ ID NO: 216, SEQ ID NO: 217, SEQ ID NO: 218, and SEQ ID NO: 219, or any combination thereof.
The delivery constructs can comprise a carrier directly coupled to a heterologous (e.g., a biologically active) cargo. The heterologous (e.g., a biologically active) cargo can be directly coupled to the C-terminus of the delivery construct. The heterologous (e.g., a biologically active) cargo can be directly coupled to the N-terminus of the delivery construct.
The delivery constructs can comprise a carrier chemically coupled to a heterologous (e.g., a biologically active) cargo. The delivery constructs can comprise a carrier recombinantly coupled to a heterologous (e.g., a biologically active) cargo. A delivery construct of the present disclosure can be produced partly synthetically (e.g., via solid-phase synthesis) or recombinantly (e.g., bacterially expressed (e.g., E. coli) or in a mammalian cell (e.g., CHO cell)). A delivery construct of the present disclosure can be produced partly synthetic and partly recombinant.
The delivery constructs can comprise a delivery construct coupled to a biologically active cargo by a cleavable spacer. The spacer can be cleavable by an enzyme that is present at a basolateral membrane of a polarized epithelial cell. The spacer can be cleavable by an enzyme that is present in the plasma. The cleavable spacer can comprise the amino acid sequence set forth in any one of SEQ ID NO: 174-SEQ ID NO: 206. The cleavable spacer can be a spacer that comprises an amino acid sequence that can be a known substrate for the tobacco etch virus (TEV) protease. The cleavable spacer comprises the amino acid sequence set in forth in SEQ ID NO: 193. The spacer can be cleavable by an enzyme that is present at a basal-lateral membrane of a polarized epithelial cell. The spacer can be cleavable by an enzyme that is present in the plasma of a subject.
The cleavable spacers can comprise a peptide sequence (or like domain), which serves to inhibit, interfere with, or block the ability of the biologically active cargo to bind to receptors at the surface of epithelial cells, but wherein the delivery construct retains the ability of the cargo to activate it's receptor after the delivery construct is transported across the epithelial barrier and the cargo is released from the delivery construct and spacer components of the construct. The cleavable spacer can comprise the amino acid sequence set forth in, e.g., SEQ ID NO: 194-SEQ ID NO: 206.
The present disclosure also relates to pharmaceutical compositions that can comprise a novel non-naturally occurring delivery construct of the present disclosure and one or more pharmaceutically acceptable carriers, formulated for oral administration, topical administration, pulmonary administration, intra-nasal administration, buccal administration, sublingual administration or ocular administration.
The present disclosure provides a method of treating an inflammatory disease in a subject that can comprise administering a pharmaceutical composition of the present disclosure to the subject. In various embodiments, the inflammatory disease is selected from an inflammatory bowel disease, psoriasis or bacterial sepsis. In various embodiments, the inflammatory bowel disease is Crohn's disease, ulcerative colitis, collagenous colitis, lymphocytic colitis, ischemic colitis, diversion colitis, Behcet's syndrome or indeterminate colitis.
The present disclosure provides a method of treating an autoimmune disease in a subject that can comprise administering a pharmaceutical composition of the present disclosure to the subject. In various embodiments, the autoimmune disease is systemic lupus erythematosus (SLE), pemphigus vulgaris, myasthenia gravis, hemolytic anemia, thrombocytopenia purpura, Grave's disease, Sjogren's disease, dermatomyositis, Hashimoto's disease, polymyositis, inflammatory bowel disease, multiple sclerosis (MS), diabetes mellitus, rheumatoid arthritis, or scleroderma.
The present disclosure provides a method of treating a cancer in a subject that can comprise administering a pharmaceutical composition of the present disclosure to the subject. In various embodiments, the cancer to be treated includes, but is not limited to, non-Hodgkin's lymphomas, Hodgkin's lymphoma, chronic lymphocytic leukemia, hairy cell leukemia, acute lymphoblastic leukemia, multiple myeloma, carcinomas of the bladder, kidney ovary, cervix, breast, lung, nasopharynx, malignant melanoma and rituximab resistant NHL and leukemia.
The present disclosure provides a method of treating a subject having a metabolic disorder, said method can comprise administering a pharmaceutical composition of the present disclosure in an amount sufficient to treat said disorder, wherein said metabolic disorder is diabetes, obesity, diabetes as a consequence of obesity, hyperglycemia, dyslipidemia, hypertriglyceridemia, syndrome X, insulin resistance, impaired glucose tolerance (IGT), diabetic dyslipidemia, or hyperlipidemia.
The present disclosure provides a method of treating a subject having a fatty liver disease (e.g., nonalcoholic fatty liver disease (NAFLD); nonalcoholic steatohepatitis (NASH)), a gastrointestinal disease, or a neurodegenerative disease, said method comprising orally administering a pharmaceutical composition of the present disclosure in an amount sufficient to treat said disease.
The present disclosure provides a method of treating a subject having a GH deficient growth disorder, said method can comprise administering a pharmaceutical composition of the present disclosure in an amount sufficient to treat said disorder, wherein said disorder is growth hormone deficiency (GHD), Turner syndrome (TS), Noonan syndrome, Prader-Willi syndrome, short stature homeobox-containing gene (SHOX) deficiency, chronic renal insufficiency, and idiopathic short stature short bowel syndrome, GH deficiency due to rare pituitary tumors or their treatment, and muscle-wasting disease associated with HIV/AIDS.
A delivery construct can comprise a carrier comprising an amino acid sequence having at least 80% sequence identity to any one or more of the amino acid sequences set forth in SEQ ID NO: 1-SEQ ID NO: 133 or SEQ ID NO: 137-SEQ ID NO: 147. A delivery construct can comprise a carrier comprising an amino acid sequence having at least 90% sequence identity to any one or more of the amino acid sequences set forth in SEQ ID NO: 1-SEQ ID NO: 133 or SEQ ID NO: 137-SEQ ID NO: 147. A delivery construct can comprise a carrier comprising an amino acid sequence having at least 95% sequence identity to any one or more of the amino acid sequences set forth in SEQ ID NO: 1-SEQ ID NO: 133 or SEQ ID NO: 137-SEQ ID NO: 147. A delivery construct can comprise a carrier comprising an amino acid sequence having at least 99% sequence identity to any one or more of the amino acid sequences set forth in SEQ ID NO: 1-SEQ ID NO: 133 or SEQ ID NO: 137-SEQ ID NO: 147. The carrier can be derived from a Cholix domain I and can comprise an amino acid sequence having at least 80% sequence identity to any one or more of the amino acid sequences set forth in SEQ ID NO: 4-SEQ ID NO: 125 and/or SEQ ID NO: 148-SEQ ID NO: 152. The carrier can be derived from a Cholix domain I and can comprise an amino acid sequence having at least 90% sequence identity to any one or more of the amino acid sequences set forth in SEQ ID NO: 4-SEQ ID NO: 125 and/or SEQ ID NO: 148-SEQ ID NO: 152. The carrier can be derived from a Cholix domain I and can comprise an amino acid sequence having at least 95% sequence identity to any one or more of the amino acid sequences set forth in SEQ ID NO: 4-SEQ ID NO: 125 and/or SEQ ID NO: 148-SEQ ID NO: 152. The carrier can be derived from a Cholix domain I and can comprise an amino acid sequence having at least 99% sequence identity to any one or more of the amino acid sequences set forth in SEQ ID NO: 4-SEQ ID NO: 125 and/or SEQ ID NO: 148-SEQ ID NO: 152. Any one of these carriers can be combined with any heterologous cargo described and disclosed herein, e.g., those having at least 80% sequence identity to an amino acid sequence set forth in any one of SEQ ID NO: 214-SEQ ID NO: 220. Any one of these carriers can be combined with any heterologous cargo described and disclosed herein, e.g., those having at least 90% sequence identity to an amino acid sequence set forth in any one of SEQ ID NO: 214-SEQ ID NO: 220. Any one of these carriers can be combined with any heterologous cargo described and disclosed herein, e.g., those having at least 95% sequence identity to an amino acid sequence set forth in any one of SEQ ID NO: 214-SEQ ID NO: 220. Any one of these carriers can be combined with any heterologous cargo described and disclosed herein, e.g., those having at least 99% sequence identity to an amino acid sequence set forth in any one of SEQ ID NO: 214-SEQ ID NO: 220. A delivery construct described herein can comprise an amino acid sequence having at least 80% sequence identity to an amino acid sequence set forth in any one of SEQ ID NO: 153-SEQ ID NO: 165. A delivery construct described herein can comprise an amino acid sequence having at least 90% sequence identity to an amino acid sequence set forth in any one of SEQ ID NO: 153-SEQ ID NO: 165. A delivery construct described herein can comprise an amino acid sequence having at least 95% sequence identity to an amino acid sequence set forth in any one of SEQ ID NO: 153-SEQ ID NO: 165. A delivery construct described herein can comprise an amino acid sequence having at least 99% sequence identity to an amino acid sequence set forth in any one of SEQ ID NO: 153-SEQ ID NO: 165. A construct can be capable of endocytosis (e.g., apical endocytosis). A construct can be capable of apical-to-basal transcytosis.
The present disclosure provides isolated delivery constructs that can be capable of binding a receptor on the luminal surface of intestinal epithelial cells with sufficient affinity to allow endocytosis; wherein the domain is a polypeptide comprising an amino acid sequence wherein one or more amino acid residues of one bacterial toxin domain I polypeptide is replaced by one or more amino acid residues of a second bacterial toxin (e.g., an exotoxin) domain I polypeptide. The domain I of a first exotoxin can comprise a polypeptide which comprises an amino acid sequence wherein one or more amino acid residues of SEQ ID NO: 4 can be replaced by one or more amino acid residues of a second bacterial toxin (e.g., an exotoxin) receptor binding domain polypeptide. The receptor binding domain can be a polypeptide which comprises an amino acid sequence wherein one or more amino acid residues of SEQ ID NO: 4 is replaced by one or more amino acid residues of SEQ ID NO: 137. The receptor binding domain can be a polypeptide which comprises an amino acid sequence wherein one or more amino acid residues of SEQ ID NO: 137 is replaced by one or more amino acid residues a second bacterial toxin receptor binding domain polypeptide. The receptor binding domain can be a polypeptide which comprises an amino acid sequence wherein one or more amino acid residues of SEQ ID NO: 136 is replaced by one or more amino acid residues of SEQ ID NO: 4. A chimeric carrier can comprise a biologically active cargo coupled to the polypeptide to produce a chimeric construct; wherein the chimeric construct is capable of delivering the biologically active cargo.
The present disclosure provides a chimeric construct comprising a bacterial toxin-derived delivery construct; and a biologically active cargo; wherein the delivery construct is capable of delivering the biologically active cargo into an epithelial cell; and wherein the delivery construct does not comprise a bacterial toxin-derived translocation domain or a bacterial toxin-derived catalytic (cytotoxic) domain. The present disclosure provides a chimeric construct consisting of a receptor binding domain of a bacterial toxin; and a biologically active cargo; wherein the delivery construct is capable of delivering the biologically active cargo into an epithelial cell, and wherein the chimeric construct is capable of binding a receptor on the luminal surface of intestinal epithelial cells.
The present disclosure further provides polynucleotides that encode the non-naturally occurring delivery constructs and/or delivery constructs of the present disclosure; vectors comprising polynucleotides encoding the non-naturally occurring delivery constructs and/or delivery constructs of the present disclosure; optionally, operably-linked to control sequences recognized by a host cell transformed with the vector; host cells comprising vectors comprising polynucleotides encoding the non-naturally occurring delivery constructs and/or delivery constructs of the present disclosure; a process for producing the non-naturally occurring delivery constructs and/or delivery constructs of the present disclosure comprising culturing host cells comprising vectors comprising polynucleotides encoding the non-naturally occurring delivery constructs and/or delivery constructs of the present disclosure such that the polynucleotide is expressed; and, optionally, recovering the non-naturally occurring delivery constructs and/or delivery constructs from host cell culture medium.
Disclosed herein is a use of a non-naturally occurring delivery construct of the present disclosure for the preparation of a medicament for treatment, prophylaxis and/or prevention of an inflammatory disease in a subject in need thereof.
Disclosed herein is a use of a non-naturally occurring delivery construct of the present disclosure for the preparation of a medicament for treatment, prophylaxis and/or prevention of an autoimmune disease in a subject in need thereof.
Disclosed herein is a use of a non-naturally occurring delivery construct of the present disclosure for the preparation of a medicament for treatment, prophylaxis and/or prevention of a cancer in a subject in need thereof.
Disclosed herein is a use of a non-naturally occurring delivery construct of the present disclosure for the preparation of a medicament for treatment, prophylaxis and/or prevention of a metabolic disorder in a subject in need thereof.
Disclosed herein is a use of a non-naturally occurring delivery construct of the present disclosure for the preparation of a medicament for treatment, prophylaxis and/or prevention of a fatty liver disease in a subject in need thereof.
Disclosed herein is a use of a non-naturally occurring delivery construct of the present disclosure for the preparation of a medicament for treatment, prophylaxis and/or prevention of GH deficient growth disorder in a subject in need thereof.
The novel features of the present disclosure are set forth with particularity in the appended claims. A better understanding of the features and advantages of the present disclosure will be obtained by reference to the following detailed description that sets forth illustrative aspects, in which the principles of the disclosure are utilized, and the accompanying drawings (also “Figure” and “FIG.” herein), of which:
While various embodiments of the invention have been shown and described herein, it will be obvious to those skilled in the art that such embodiments are provided by way of example only. Numerous variations, changes, and substitutions may occur to those skilled in the art without departing from the invention. It should be understood that various alternatives to the embodiments of the invention described herein may be employed.
The present disclosure provides methods and compositions for transport and/or delivery of a cargo molecule to certain location(s) within a cell (e.g., a supranuclear location) or across a cell (e.g., epithelial cell), either in vitro or in vivo (e.g., in a rodent or a human). Such cargo can be directed to a set of location(s) by coupling it to a carrier molecule. Such carrier molecule can interact with unique receptors both on the cell surface and intracellularly for the targeted delivery of the cargo. Various such carrier, cargos, and uses thereof are described herein.
Unless otherwise defined herein, scientific and technical terms used in connection with the present disclosure shall have the meanings that are commonly understood by those of ordinary skill in the art. Further, unless otherwise required by context, singular terms shall include pluralities and plural terms shall include the singular. Generally, nomenclatures used in connection with, and techniques of, cell and tissue culture, molecular biology, immunology, microbiology, genetics, protein and nucleic acid chemistry, and hybridization described herein are those commonly used and well known in the art. The methods and techniques of the present disclosure are generally performed according to conventional methods well known in the art and as described in various general and more specific references that are cited and discussed throughout the present specification unless otherwise indicated. See, e.g., Green and Sambrook, Molecular Cloning: A Laboratory Manual, 4th ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. (2012) and Ausubel et al., Current Protocols in Molecular Biology, Greene Publishing Associates (1992), each incorporated herein by reference. Enzymatic reactions and purification techniques are performed according to manufacturer's specifications, as commonly accomplished in the art or as described herein. The nomenclature used in connection with, and the laboratory procedures and techniques of, analytical chemistry, synthetic organic chemistry, and medicinal and pharmaceutical chemistry described herein are those commonly used and well known in the art. Standard techniques are used for chemical syntheses, chemical analyses, pharmaceutical preparation, formulation, and delivery, and treatment of patients.
As described herein, an amino acid sequence can comprise one or more modification to the amino acid sequences at the N-terminus. An amino acid sequence as disclosed herein can comprise an “N-cap.” Generally, an N-cap as disclosed herein can refer to a modification of an N-terminus of a peptide or polypeptide in a variety of ways, and particularly can refer to (i) the addition of one or more amino acid sequences or other moieties (e.g., affinity handles, cell-penetrating peptide sequences, etc.), and (ii) a modification of one or more amino acid residues within the first 1-10 N-terminal amino acids of a peptide or polypeptide, wherein the amino acid modification is relative to a reference sequence or a consensus sequence (see e.g., comparison of the first 4 N-terminal amino acid residues of polypeptide sequences set forth in SEQ ID NO: 4 and SEQ ID NO: 5, or SEQ ID NO: 1 and SEQ ID NO: 2 as described herein). An N-cap can comprise an additional 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, or 15 or 100 additional amino acid residues that are attached to (e.g., chemically coupled to) to the N-terminus of an amino acid sequence, such as a Cholix derived carrier molecule. An N-cap can further comprise one or more variations in the amino acid sequence at the N-terminus. For example, a Cholix domain I derived carrier can comprise an N-cap. The N-cap can comprise substituting one or more N-terminal amino acid residues with other amino acid residues. An N-cap can further comprise an N-terminal methionine residue. One or more of these modifications can be a result of producing the Cholix domain I amino acid sequence in a bacterial production system (e.g., E. coli). As an example, Cholix domain I can comprise amino acid residues 1-265 of SEQ ID NO: 1 which is set forth in SEQ ID NO: 4. A bacterially expressed Cholix domain can comprise an amino acid sequence set forth in SEQ ID NO: 5, which as SEQ ID NO: 4 plus an N-terminal methionine residues, which can also be referred to herein as M+Cholix1-265 or M+Cholix265.
As described herein, the term “lacks a domain” or “lacking a domain” generally refers to not comprising a complete domain, but optionally comprising a portion or fragment thereof. For example, a carrier that is derived from a domain I of an exotoxin but lacks a domain II, a domain Ib, and a domain III of said exotoxin generally refers to a carrier that does not comprise the full amino acid sequences of (e.g., 100% sequence identity to) any one of the domains II, Ib, and III, but which can optionally comprise portions or fragments thereof. Thus, a carrier derived from a Cholix domain and lacking a Cholix domain II as described herein can comprise Cholix domain I having an amino acid sequence set forth in SEQ ID NO: 4 or SEQ ID NO: 5 and an additional 50-80 amino acid residues of Cholix domain II (e.g., amino acids 1-50 or 1-80 of SEQ ID NO: 126), and or an additional 50-80 amino acid residues of Cholix domain III (e.g., amino acids 1-50 or 1-80 of SEQ ID NO: 128).
As described herein, the terms “attached to”, “coupled to”, “linked to”, “conjugated to” and “fused to” can be used interchangeably and generally mean that a first molecule (e.g., a polypeptide) is associated with a second molecule (e.g., a polypeptide, small molecule, etc.). The association can be via a chemical linkage, wherein the chemical linkage can be covalently or non-covalently. A covalent chemical linkage between a first polypeptide and a second polypeptide can be produced by synthetically coupling the first polypeptide to the second polypeptide, or it can be produced by recombinant fusion of the first polypeptide to the second polypeptide. Thus, a first (e.g., a first polypeptide) molecule can be chemically (e.g., synthetically) or recombinantly coupled to a second molecule (e.g., a second polypeptide).
The terms “polypeptide”, “peptide” and “protein” are used interchangeably herein to refer to a polymer of amino acid residues. In addition, the terms “toxin”, “carrier”, “delivery construct”, “chimeric construct”, “protein”, and “polypeptide” can be used interchangeably and generally refer to a molecule that can be coupled to a heterologous cargo. Generally, “delivery constructs” and “chimeric constructs” are “peptides”, “polypeptides”, or “proteins”, are described herein as chains of amino acids whose alpha carbons are linked through peptide bonds. The terminal amino acid at one end of the chain (amino terminal) therefore has a free amino group, while the terminal amino acid at the other end of the chain (carboxy terminal) has a free carboxyl group. As used herein, the term “amino terminus” (abbreviated N-terminus) refers to the free α-amino group on an amino acid at the amino terminal of a peptide or to the α-amino group (imino group when participating in a peptide bond) of an amino acid at any other location within the peptide. Similarly, the term “carboxy terminus” refers to the free carboxyl group on the carboxy terminus of a peptide or the carboxyl group of an amino acid at any other location within the peptide. Peptides also include essentially any polyamino acid including, but not limited to, peptide mimetics such as amino acids joined by an ether bond as opposed to an amide bond. Generally, peptides, polypeptide, and proteins as described herein can be recombinantly produced or chemically synthesized (e.g., using solid-phase synthesis), or a combination thereof.
As disclosed herein, the term “delivery” generally refers to the presence of a molecule (e.g., a heterologous cargo) at a location (e.g., an intracellular compartment or a supranuclear region) for a certain period of time. The term “delivery” can refer to the presence of a molecule (e.g., a heterologous cargo) at a location (e.g., an intracellular compartment or a supranuclear region) for a time that is sufficient to elicit a certain biological effect, such as an interaction (e.g., binding) with a protein (e.g., an enzyme or a receptor) at that location. The delivery of a molecule (e.g., a heterologous cargo) to a location (e.g., an intracellular compartment or a supranuclear region) can refer to the retention of the molecule at that location. Retention of a molecule at a certain intracellular or extracellular region or compartment can be for a certain amount of time, e.g., at least 2 minutes, at least 5 minutes, at least 10 minutes, at least 15 minutes, at 30 minutes, or at least 60 minutes. Retention of a molecule can depend on various factors such as the location where the molecule is retained and/or the types of molecular interactions that occur between the molecule (e.g., a carrier, a delivery construct, and/or a heterologous cargo). For example, delivery of a heterologous cargo to a basolateral compartment via transcytosis across a polarized epithelial cell can comprise retaining the heterologous cargo at the basolateral location for a time sufficient to elicit a certain effect, such as a therapeutic effect in case of a therapeutic and/or biologically active cargo.
Polypeptides of the disclosure include polypeptides that have been modified in any way and for any reason, for example, to: (1) reduce susceptibility to proteolysis, (2) reduce susceptibility to oxidation, (3) alter binding affinity for forming protein complexes, (4) alter binding affinities, and (5) confer or modify other physicochemical or functional properties. For example, single or multiple amino acid substitutions (e.g., conservative amino acid substitutions) can be made in the naturally occurring sequence (e.g., in the portion of the polypeptide outside the domain(s) forming intermolecular contacts). A “conservative amino acid substitution” refers to the substitution in a polypeptide of an amino acid with a functionally similar amino acid. The following six groups each contain amino acids that are conservative substitutions for one another:
A “non-conservative amino acid substitution” refers to the substitution of a member of one of these classes for a member from another class. In making such changes, according to various embodiments, the hydropathic index of amino acids can be considered. Each amino acid has been assigned a hydropathic index on the basis of its hydrophobicity and charge characteristics. They are: isoleucine (+4.5); valine (+4.2); leucine (+3.8); phenylalanine (+2.8); cysteine/cystine (+2.5); methionine (+1.9); alanine (+1.8); glycine (−0.4); threonine (−0.7); serine (−0.8); tryptophan (−0.9); tyrosine (−1.3); proline (−1.6); histidine (−3.2); glutamate (−3.5); glutamine (−3.5); aspartate (−3.5); asparagine (−3.5); lysine (−3.9); and arginine (−4.5). In other embodiments, the carrier of a delivery constructs is a chimeric carrier comprising a peptide, polypeptide, small molecule, aptamer, fragments thereof, or any combination thereof.
The importance of the hydropathic amino acid index in conferring interactive biological function on a protein is understood in the art (see, for example, Kyte et al., 1982, J. Mol. Biol. 157:105-131). It is known that certain amino acids can be substituted for other amino acids having a similar hydropathic index or score and still retain a similar biological activity. In making changes based upon the hydropathic index, in various embodiments, the substitution of amino acids whose hydropathic indices are within +2 is included. In various embodiments, those that are within +1 are included, and in various embodiments, those within +0.5 are included.
It is also understood in the art that the substitution of like amino acids can be made effectively on the basis of hydrophilicity, particularly where the biologically functional protein or peptide thereby created is intended for use in immunological applications, as disclosed herein. In various embodiments, the greatest local average hydrophilicity of a protein, as governed by the hydrophilicity of its adjacent amino acids, correlates with its immunogenicity and antigenicity, i.e., with a biological property of the protein.
The following hydrophilicity values have been assigned to these amino acid residues: arginine (+3.0); lysine (+3.0); aspartate (+3.0+/−0.1); glutamate (+3.0+/−0.1); serine (+0.3); asparagine (+0.2); glutamine (+0.2); glycine (0); threonine (−0.4); proline (−0.5+/−0.1); alanine (−0.5); histidine (−0.5); cysteine (−1.0); methionine (−1.3); valine (−1.5); leucine (−1.8); isoleucine (−1.8); tyrosine (−2.3); phenylalanine (−2.5) and tryptophan (−3.4). In making changes based upon similar hydrophilicity values, in various embodiments, the substitution of amino acids whose hydrophilicity values are within ±2 is included, in various embodiments, those that are within ±1 are included, and in various embodiments, those within ±0.5 are included.
Exemplary amino acid substitutions are set forth in TABLE 1.
A skilled artisan will be able to determine suitable variants of polypeptides as set forth herein using well-known techniques. One skilled in the art can identify suitable areas of the molecule that can be changed without destroying activity by targeting regions not believed to be important for activity. The skilled artisan can identify residues and portions of the molecules that are conserved among similar polypeptides. Areas of these materials that can be important for biological activity or for structure could be subjected to conservative amino acid substitutions without destroying the biological activity or without adversely affecting the polypeptide structure.
Additionally, one skilled in the art can review structure-function studies identifying residues in similar polypeptides that are important for activity or structure. In view of such a comparison, the skilled artisan can predict the importance of amino acid residues in a polypeptide that correspond to amino acid residues important for activity or structure in similar polypeptides. One skilled in the art can opt for chemically similar amino acid substitutions for such predicted important amino acid residues.
One skilled in the art can also analyze the three-dimensional structure and amino acid sequence in relation to that structure in similar polypeptides. In view of such information, one skilled in the art can predict the alignment of amino acid residues of a polypeptide with respect to its three-dimensional structure. One skilled in the art can choose to not make radical changes to amino acid residues predicted to be on the surface of the polypeptide, since such residues can be involved in important interactions with other molecules. Moreover, one skilled in the art can generate test variants containing a single amino acid substitution at each desired amino acid residue. The variants can then be screened using activity assays known to those skilled in the art. Such variants could be used to gather information about suitable variants. For example, if one discovered that a change to a particular amino acid residue resulted in destroyed, undesirably reduced, or unsuitable activity, variants with such a change in the amino acid sequence can be avoided. In other words, based on information gathered from such routine experiments, one skilled in the art can readily determine the amino acids where further substitutions should be avoided either alone or in combination with other mutations.
The term “polypeptide fragment” and “truncated polypeptide” as used herein refers to a polypeptide that has an amino-terminal and/or carboxy-terminal deletion as compared to a corresponding full-length protein. In various embodiments, fragments can be, e.g., at least 5, at least 10, at least 25, at least 50, at least 100, at least 150, at least 200, at least 250, at least 300, at least 350, at least 400, at least 450, at least 500, at least 600, at least 700, at least 800, at least 900 or at least 1000 amino acids in length. In various embodiments, fragments can also be, e.g., at most 1000, at most 900, at most 800, at most 700, at most 600, at most 500, at most 450, at most 400, at most 350, at most 300, at most 250, at most 200, at most 150, at most 100, at most 50, at most 25, at most 10, or at most 5 amino acids in length. A fragment can further comprise, at either or both of its ends, one or more additional amino acids, for example, a sequence of amino acids from a different naturally-occurring protein (e.g., an Fc or leucine zipper domain) or an artificial amino acid sequence (e.g., an artificial spacer sequence).
The terms “polypeptide variant” and “polypeptide mutant” as used herein refer to a polypeptide that comprises an amino acid sequence wherein one or more amino acid residues are inserted into, deleted from and/or substituted into the amino acid sequence relative to another polypeptide sequence. The number of amino acid residues to be inserted, deleted, or substituted can be, e.g., at least 1, at least 2, at least 3, at least 4, at least 5, at least 10, at least 25, at least 50, at least 75, at least 100, at least 125, at least 150, at least 175, at least 200, at least 225, at least 250, at least 275, at least 300, at least 350, at least 400, at least 450 or at least 500 amino acids in length. Variants of the present disclosure include fusion proteins.
A “derivative” of a polypeptide is a polypeptide that has been chemically modified, e.g., conjugation to another chemical moiety such as, for example, polyethylene glycol, albumin (e.g., human serum albumin), phosphorylation, and glycosylation.
The term “% sequence identity” is used interchangeably herein with the term “% identity” and refers to the level of amino acid sequence identity between two or more peptide sequences or the level of nucleotide sequence identity between two or more nucleotide sequences, when aligned using a sequence alignment program. For example, as used herein, 80% identity means the same thing as 80% sequence identity determined by a defined algorithm, and means that a given sequence is at least 80% identical to another length of another sequence. In various embodiments, the % identity is selected from, e.g., at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, or at least 99% or more sequence identity to a given sequence. In various embodiments, the % identity is in the range of, e.g., about 60% to about 70%, about 70% to about 80%, about 80% to about 85%, about 85% to about 90%, about 90% to about 95%, or about 95% to about 99%.
The term “% sequence homology” is used interchangeably herein with the term “% homology” and refers to the level of amino acid sequence homology between two or more peptide sequences or the level of nucleotide sequence homology between two or more nucleotide sequences, when aligned using a sequence alignment program. For example, as used herein, 80% homology means the same thing as 80% sequence homology determined by a defined algorithm, and accordingly a homologue of a given sequence has greater than 80% sequence homology over a length of the given sequence. In various embodiments, the % homology is selected from, e.g., at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, or at least 99% or more sequence homology to a given sequence. In various embodiments, the % homology is in the range of, e.g., about 60% to about 70%, about 70% to about 80%, about 80% to about 85%, about 85% to about 90%, about 90% to about 95%, or about 95% to about 99%.
Exemplary computer programs which can be used to determine identity between two sequences include, but are not limited to, the suite of BLAST programs, e.g., BLASTN, BLASTX, TBLASTX, BLASTP, and TBLASTN, publicly available on the Internet at the NCBI website. See also Altschul et al., 1990, J. Mol. Biol. 215:403-10 (with special reference to the published default setting, i.e., parameters w=4, t=17) and Altschul et al., 1997, Nucleic Acids Res., 25:3389-3402. Sequence searches are typically carried out using the BLASTP program when evaluating a given amino acid sequence relative to amino acid sequences in the GenBank Protein Sequences and other public databases. The BLASTX program is preferred for searching nucleic acid sequences that have been translated in all reading frames against amino acid sequences in the GenBank Protein Sequences and other public databases. Both BLASTP and BLASTX are run using default parameters of an open gap penalty of 11.0, and an extended gap penalty of 1.0, and utilize the BLOSUM-62 matrix. See id.
In addition to calculating percent sequence identity, the BLAST algorithm also performs a statistical analysis of the similarity between two sequences (see, e.g., Karlin & Altschul, Proc. Nat'l. Acad. Sci. USA, 90:5873-5787 (1993)). One measure of similarity provided by the BLAST algorithm is the smallest sum probability (P(N)), which provides an indication of the probability by which a match between two nucleotide or amino acid sequences would occur by chance. For example, a nucleic acid is considered similar to a reference sequence if the smallest sum probability in a comparison of the test nucleic acid to the reference nucleic acid is, e.g., at most 0.1, at most 0.01, or at most 0.001.
“Polynucleotide” refers to a polymer composed of nucleotide units. Polynucleotides include naturally occurring nucleic acids, such as deoxyribonucleic acid (“DNA”) and ribonucleic acid (“RNA”) as well as nucleic acid analogs. Nucleic acid analogs include those which include non-naturally occurring bases, nucleotides that engage in linkages with other nucleotides other than the naturally occurring phosphodiester bond or which include bases attached through linkages other than phosphodiester bonds. Thus, nucleotide analogs include, for example and without limitation, phosphorothioates, phosphorodithioates, phosphorotriesters, phosphoramidates, boranophosphates, methylphosphonates, chiral-methyl phosphonates, 2-O-methyl ribonucleotides, peptide-nucleic acids (PNAs), and the like. Such polynucleotides can be synthesized, for example, using an automated DNA synthesizer. The term “nucleic acid” typically refers to large polynucleotides. The term “oligonucleotide” typically refers to short polynucleotides, generally no greater than about 50 nucleotides. It will be understood that when a nucleotide sequence is represented by a DNA sequence (i.e., A, T, G, C), this also includes an RNA sequence (i.e., A, U, G, C) in which “U” replaces “T.”
Conventional notation is used herein to describe polynucleotide sequences: the left-hand end of a single-stranded polynucleotide sequence is the 5′-end; the left-hand direction of a double-stranded polynucleotide sequence is referred to as the 5′-direction. The direction of 5′ to 3′ addition of nucleotides to nascent RNA transcripts is referred to as the transcription direction. The DNA strand having the same sequence as an mRNA is referred to as the “coding strand”; sequences on the DNA strand having the same sequence as an mRNA transcribed from that DNA and which are located 5′ to the 5′-end of the RNA transcript are referred to as “upstream sequences”; sequences on the DNA strand having the same sequence as the RNA and which are 3′ to the 3′ end of the coding RNA transcript are referred to as “downstream sequences.”
“Complementary” refers to the topological compatibility or matching together of interacting surfaces of two polynucleotides. Thus, the two molecules can be described as complementary, and furthermore, the contact surface characteristics are complementary to each other. A first polynucleotide is complementary to a second polynucleotide if the nucleotide sequence of the first polynucleotide is substantially identical to the nucleotide sequence of the polynucleotide binding partner of the second polynucleotide, or if the first polynucleotide can hybridize to the second polynucleotide under stringent hybridization conditions.
“Hybridizing specifically to” or “specific hybridization” or “selectively hybridize to”, refers to the binding, duplexing, or hybridizing of a nucleic acid molecule preferentially to a particular nucleotide sequence under stringent conditions when that sequence is present in a complex mixture (e.g., total cellular) DNA or RNA. The term “stringent conditions” refers to conditions under which a probe will hybridize preferentially to its target subsequence, and to a lesser extent to, or not at all to, other sequences. “Stringent hybridization” and “stringent hybridization wash conditions” in the context of nucleic acid hybridization experiments such as Southern and northern hybridizations are sequence-dependent, and are different under different environmental parameters. An extensive guide to the hybridization of nucleic acids can be found in Tijssen, 1993, Laboratory Techniques in Biochemistry and Molecular Biology—Hybridization with Nucleic Acid Probes, part I, chapter 2, “Overview of principles of hybridization and the strategy of nucleic acid probe assays”, Elsevier, N.Y.; Sambrook et al., 2001, Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory, 3.sup.rd ed., NY; and Ausubel et al., eds., Current Edition, Current Protocols in Molecular Biology, Greene Publishing Associates and Wiley Interscience, NY.
Generally, highly stringent hybridization and wash conditions are selected to be about 5° C. lower than the thermal melting point (Tm) for the specific sequence at a defined ionic strength and pH. The Tm is the temperature (under defined ionic strength and pH) at which 50% of the target sequence hybridizes to a perfectly matched probe. Very stringent conditions are selected to be equal to the Tm for a particular probe. An example of stringent hybridization conditions for hybridization of complementary nucleic acids which have more than about 100 complementary residues on a filter in a Southern or northern blot is 50% formalin with 1 mg of heparin at 42° C., with the hybridization being carried out overnight. An example of highly stringent wash conditions is 0.15 M NaCl at 72° C. for about 15 minutes. An example of stringent wash conditions is a 0.2×SSC wash at 65° C. for 15 minutes. See Sambrook et al. for a description of SSC buffer. A high stringency wash can be preceded by a low stringency wash to remove background probe signal. An exemplary medium stringency wash for a duplex of, e.g., more than about 100 nucleotides, is 1×SSC at 45° C. for 15 minutes. An exemplary low stringency wash for a duplex of, e.g., more than about 100 nucleotides, is 4-6×SSC at 40° C. for 15 minutes. In general, a signal to noise ratio of 2× (or higher) than that observed for an unrelated probe in the particular hybridization assay indicates detection of a specific hybridization.
“Primer” refers to a polynucleotide that is capable of specifically hybridizing to a designated polynucleotide template and providing a point of initiation for synthesis of a complementary polynucleotide. Such synthesis occurs when the polynucleotide primer is placed under conditions in which synthesis is induced, i.e., in the presence of nucleotides, a complementary polynucleotide template, and an agent for polymerization such as DNA polymerase. A primer is typically single-stranded, but can be double-stranded. Primers are typically deoxyribonucleic acids, but a wide variety of synthetic and naturally occurring primers are useful for many applications. A primer is complementary to the template to which it is designed to hybridize to serve as a site for the initiation of synthesis, but need not reflect the exact sequence of the template. In such a case, specific hybridization of the primer to the template depends on the stringency of the hybridization conditions. Primers can be labeled with, e.g., chromogenic, radioactive, or fluorescent moieties and used as detectable moieties.
“Probe,” when used in reference to a polynucleotide, refers to a polynucleotide that is capable of specifically hybridizing to a designated sequence of another polynucleotide. A probe specifically hybridizes to a target complementary polynucleotide, but need not reflect the exact complementary sequence of the template. In such a case, specific hybridization of the probe to the target depends on the stringency of the hybridization conditions. Probes can be labeled with, e.g., chromogenic, radioactive, or fluorescent moieties and used as detectable moieties. In instances where a probe provides a point of initiation for synthesis of a complementary polynucleotide, a probe can also be a primer.
A “vector” is a polynucleotide that can be used to introduce other nucleic acids linked to it into a cell. One type of vector is a “plasmid,” which refers to a linear or circular double stranded DNA molecule into which additional nucleic acid segments can be ligated. Another type of vector is a viral vector (e.g., replication defective retroviruses, adenoviruses and adeno-associated viruses), wherein additional DNA segments can be introduced into the viral genome. Certain vectors are capable of autonomous replication in a host cell into which they are introduced (e.g., bacterial vectors comprising a bacterial origin of replication and episomal mammalian vectors). Other vectors (e.g., non-episomal mammalian vectors) are integrated into the genome of a host cell upon introduction into the host cell, and thereby are replicated along with the host genome. An “expression vector” is a type of vector that can direct the expression of a chosen polynucleotide.
A “regulatory sequence” is a nucleic acid that affects the expression (e.g., the level, timing, or location of expression) of a nucleic acid to which it is operably linked. The regulatory sequence can, for example, exert its effects directly on the regulated nucleic acid, or through the action of one or more other molecules (e.g., polypeptides that bind to the regulatory sequence and/or the nucleic acid). Examples of regulatory sequences include promoters, enhancers and other expression control elements (e.g., polyadenylation signals). Further examples of regulatory sequences are described in, for example, Goeddel, 1990, Gene Expression Technology: Methods in Enzymology 185, Academic Press, San Diego, Calif. and Baron et al., 1995, Nucleic Acids Res. 23:3605-06. A nucleotide sequence is “operably linked” to a regulatory sequence if the regulatory sequence affects the expression (e.g., the level, timing, or location of expression) of the nucleotide sequence.
Generally, a cell of the present disclosure can be a eukaryotic cell or a prokaryotic cell. A cell can be an epithelial cell. An epithelial cell can be a polarized epithelial cell (e.g., a Caco-2 cell or a Chinese Hamster Ovary (CHO) cell). A cell can be an animal cell or a plant cell. An animal cell can include a cell from a marine invertebrate, fish, insects, amphibian, reptile, or mammal. A mammalian cell can be obtained from a primate, ape, equine, bovine, porcine, canine, feline, or rodent. A mammal can be a primate, ape, dog, cat, rabbit, ferret, or the like. A rodent can be a mouse, rat, hamster, gerbil, hamster, chinchilla, or guinea pig. A bird cell can be from a canary, parakeet or parrots. A reptile cell can be from a turtles, lizard or snake. A fish cell can be from a tropical fish. For example, the fish cell can be from a zebrafish (e.g., Danino rerio). A worm cell can be from a nematode (e.g., C. elegans). An amphibian cell can be from a frog. An arthropod cell can be from a tarantula or hermit crab.
A mammalian cell can also include cells obtained from a primate (e.g., a human or a non-human primate). A mammalian cell can include a blood cell, a stem cell, an epithelial cell, connective tissue cell, hormone secreting cell, a nerve cell, a skeletal muscle cell, or an immune system cell. In preferred embodiments, the methods and compositions of the present disclosure are used in combination with one or more mammalian blood cells.
A “host cell” is a cell that can be used to express a polynucleotide of the disclosure. A host cell can be a prokaryote, for example, E. coli, or it can be a eukaryote, for example, a single-celled eukaryote (e.g., a yeast or other fungus), a plant cell (e.g., a tobacco or tomato plant cell), an animal cell (e.g., a human cell, a monkey cell, a hamster cell, a rat cell, a mouse cell, or an insect cell) or a hybridoma. Typically, a host cell is a cultured cell that can be transformed or transfected with a polypeptide-encoding series of nucleic acids, which can then be expressed in the host cell. The phrase “recombinant host cell” can be used to denote a host cell that has been transformed or transfected with a polypeptide-encoding series of nucleic acids to be expressed. A host cell also can be a cell that comprises series of nucleic acids but does not express these at a desired level unless a regulatory sequence is introduced into the host cell such that it becomes operably linked with the nucleic acid. It is understood that the term host cell refers not only to the particular subject cell but to the progeny or potential progeny of such a cell. Because certain modifications can occur in succeeding generations due to, e.g., mutation or environmental influence, such progeny may not, in fact, be identical to the parent cell, but are still included within the scope of the term as used herein.
The term “isolated molecule” (where the molecule is, for example, a polypeptide such as a carrier or a delivery construct, or a polynucleotide) is a molecule that by virtue of its origin or source of derivation (1) is not associated with naturally associated components that accompany it in its native state, (2) is substantially free of other molecules from the same species (3) is expressed by a cell from a different species, or (4) does not occur in nature. Thus, a molecule that is chemically synthesized, or expressed in a cellular system different from the cell from which it naturally originates, will be “isolated” from its naturally associated components. A molecule also can be rendered substantially free of naturally associated components by isolation, using purification techniques well known in the art. Molecule purity or homogeneity can be assayed by a number of means well known in the art. For example, the purity of a polypeptide sample can be assayed using polyacrylamide gel electrophoresis and staining of the gel to visualize the polypeptide using techniques well known in the art. For certain purposes, higher resolution separation techniques can be provided by using HPLC or other means well known in the art for purification.
As disclosed herein, the terms “complete transcytosis”, “efficient transcytosis”, or “transcytosis”, or “transport” can be used interchangeably and can refer to the transport of toxin-derived delivery constructs across epithelial layers such as the gut epithelium. These terms can refer to a complete transport of these construct as determined in the respective experiment using various techniques to assess transcytosis efficiency, such as fluorescence microscopy.
As used herein, the terms “comprising” and “having” can be used interchangeably. For example, the terms “a polypeptide comprising an amino acid sequence of SEQ ID NO: 1” and “a polypeptide having an amino acid sequence of SEQ ID NO: 1” can be used interchangeably.
A protein or polypeptide is “substantially pure,” “substantially homogeneous,” or “substantially purified” when at least about 60% to 75% of a sample exhibits a single species of polypeptide. The polypeptide or protein can be monomeric or multimeric. A substantially pure polypeptide or protein will typically comprise about 50%, 60%, 70%, 80% or 90% W/W of a protein sample, more usually about 95%, and e.g., will be over 99% pure. Protein purity or homogeneity can be indicated by a number of means well known in the art, such as polyacrylamide gel electrophoresis of a protein sample, followed by visualizing a single polypeptide band upon staining the gel with a stain well known in the art. For certain purposes, higher resolution separation techniques can be provided by using HPLC or other means well known in the art for purification.
As disclosed herein, a “spacer” refers to a molecule that joins two other molecules, either covalently, or through ionic, van der Waals or hydrogen bonds, e.g., a nucleic acid molecule that hybridizes to one complementary sequence at the 5′ end and to another complementary sequence at the 3′ end, thus joining two non-complementary sequences. A “cleavable spacer” refers to a spacer that can be degraded or otherwise severed to separate the two components connected by the cleavable spacer. Cleavable spacers are generally cleaved by enzymes, typically peptidases, proteases, nucleases, lipases, and the like. Cleavable spacers can also be cleaved by environmental cues, such as, for example, specific enzymatic activities, changes in temperature, pH, salt concentration, etc. when there is such a change in environment following transcytosis of the delivery constructs across a polarized epithelial membrane. Thus, a heterologous cargo (e.g., a biologically active cargo) can be released from the carrier in a pH-dependent and/or enzyme-dependent manner.
“Pharmaceutical composition” refers to a composition suitable for pharmaceutical use in an animal. A pharmaceutical composition comprises a pharmacologically effective amount of an active agent and a pharmaceutically acceptable carrier. “Pharmacologically effective amount” refers to that amount of an agent effective to produce the intended pharmacological result.
“Pharmaceutically acceptable carrier” refers to any of the standard pharmaceutical carriers, vehicles, buffers, and excipients, such as a phosphate buffered saline solution, 5% aqueous solution of dextrose, and emulsions, such as an oil/water or water/oil emulsion, and various types of wetting agents and/or adjuvants. Suitable pharmaceutical carriers and formulations are described in Remington's Pharmaceutical Sciences, 21st Ed. 2005, Mack Publishing Co, Easton. A “pharmaceutically acceptable salt” is a salt that can be formulated into a compound for pharmaceutical use including, e.g., metal salts (sodium, potassium, magnesium, calcium, etc.) and salts of ammonia or organic amines.
The terms “treat”, “treating” and “treatment” refer to a method of alleviating or abrogating a biological disorder and/or at least one of its attendant symptoms. As used herein, to “alleviate” a disease, disorder or condition means reducing the severity and/or occurrence frequency of the symptoms of the disease, disorder, or condition. Further, references herein to “treatment” include references to curative, palliative and prophylactic treatment.
As used herein, the term “subject,” generally refers to a human or to another animal. A subject can be of any age, for example, a subject can be an infant, a toddler, a child, a pre-adolescent, an adolescent, an adult, or an elderly individual.
Ranges can be expressed herein as from “about” one particular value, and/or to “about” another particular value. When such a range is expressed, another embodiment includes from the one particular value and/or to the other particular value. Similarly, when values are expressed as approximations, by use of the antecedent “about,” it will be understood that the particular value forms another embodiment. It will be further understood that the endpoints of each of the ranges are in relation to the other endpoint, and independently of the other endpoint. The term “about” as used herein refers to a range that is 15% plus or minus from a stated numerical value within the context of the particular usage. For example, about 10 can include a range from 8.5 to 11.5.
Carriers
Contemplated herein are various carriers that can be used to deliver a cargo to a location within a cell (e.g., epithelial cell) or across a cell (e.g., epithelial cell). Such carriers can be a small molecule, a polypeptide, an aptamer, an antibody, a nucleic acid a fragment of any of the above, or a combination of any of the above.
Examples of a polypeptide contemplated herein include any polypeptide that is derived from a domain I of an exotoxin and lacking a domain II, a domain Ib and a domain III of the exotoxin. Such domain I's include but are not limited to amino acid sequences set forth in SEQ ID NO: 4, SEQ ID NO: 5, and SEQ ID NO: 137. Polypeptides that are derived from any of the above sequences include those that have a high sequence homology to the above sequences (e.g., greater than 80, 85, 90, 95, 96, 97, 98, or 99% sequence identity as defined in more detail herein). Polypeptides that are derived from any of the above sequences include those that are fragments of the above which function to deliver a cargo to a defined location within a cell or across a cell (e.g., epithelial cell).
Examples of small molecules contemplated herein include those that are rationally designed to interact with one or more of the following receptors ribophilin 1, SEC24, CK-8, TMEM132, GRP75, ERGIC-53, and/or perlecan and/or to have a similar or the same 3D structure of a domain I of an exotoxin (e.g., Cholix or PE), or a functional fragment of a domain I of an exotoxin.
Examples of antibodies, or functional binding fragments thereof, that are contemplated herein include those that are rationally designed to interact with one or more of the following receptors ribophilin 1, SEC24, CK-8, TMEM132, GRP75, ERGIC-53, and/or perlecan and/or to have a similar or the same 3D structure of a domain I of an exotoxin (e.g., Cholix or PE), or a functional fragment of a domain I of an exotoxin.
Examples of nucleic acids that are contemplated herein include those that are rationally designed to interact with one or more of the following receptors ribophilin 1, SEC24, CK-8, TMEM132, GRP75, ERGIC-53, and/or perlecan and/or to have a similar or the same 3D structure of a domain I of an exotoxin (e.g., Cholix or PE), or a functional fragment of a domain I of an exotoxin. The nucleic acid can be a mRNA, a siRNA, shRNA, or a cDNA.
The methods and compositions of the present disclosure are based on the inventors' surprising finding that a carrier capable of interacting with one or more endogenous receptors (e.g., ribophilin 1, SEC24, CK-8, TMEM132, GRP75, ERGIC-53, and/or perlecan) can provide rapid and efficient delivery of cargo into and/or across a cell such an epithelial cell.
The methods and compositions described herein allow rapid and efficient transport and/or delivery of cargo molecules across epithelial cells and/or to the interior (e.g., to the intracellular vesicle or compartment or the cytosol) of epithelial cells (e.g., polarized gut epithelial cells). The present disclosure provides constructs (e.g., isolated delivery constructs) that can comprise a carrier coupled to a heterologous cargo. A carrier as disclosed herein can vary in molecular size and composition as well as other physicochemical parameters such as isoelectric point, overall molecular net charge, etc. Generally, and as further described herein, a carrier can be a small molecule, a polypeptide, an aptamer, a nucleic acid, a fragment and/or any combination thereof.
A carrier can be derived from an exotoxin, e.g., any exotoxin described herein. For example, a carrier can be a non-naturally occurring form of Cholix exotoxin (Cholix) or
Pseudomonas exotoxin A (PE) comprising only a domain I (i.e., lacking a domain II (sometimes referred to as translocation domain), a domain Ib and a domain III (sometimes referred to as cytotoxic domain)) and can be capable of transporting and/or delivering a cargo (e.g., a heterologous cargo such as biological, therapeutic, or diagnostic molecules) across intact epithelial cells (e.g., polarized gut epithelial cells) and epithelial cell barriers (e.g., Caco-2 cell monolayers or the gut epithelium of a subject) via transcytosis and/or to the interior of an epithelial cell (e.g., via apical endocytosis and subsequent endosomal sorting and trafficking).
The present disclosure provides methods and compositions comprising a carrier, wherein the carrier can be coupled to a cargo, and as such, can deliver the cargo into or across epithelial cells. The carrier can be a polypeptide, wherein the polypeptide can be derived from an exotoxin. The exotoxin can be Cholix or PE, or any combination thereof (e.g., a carrier comprising one or more domains Cholix and PE, or truncated versions thereof). Thus, a carrier as described herein can comprise elements or portions derived from both Cholix and PE, which can be referred to a chimeric carrier. As further described herein, it was surprisingly found that a Cholix domain I or a PE domain I (e.g., SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 137), or a combination thereof, can be sufficient for rapid and efficient transport and delivery of cargo across an epithelial cell. Such transport and delivery may even be superior to the transcytosis function of the respective full-length Cholix or PE exotoxins (e.g., SEQ ID NO: 1, SEQ ID NO: 2 or SEQ ID NO: 135, respectively). The exotoxin-derived carrier polypeptides described herein can utilize endogenous trafficking pathways, including endogenous receptors and receptor complexes, to achieve apical-to-basal transcytosis and/or uptake into the interior of a cell, such as an epithelial cell (e.g., enterocytes). The delivery carriers of the present disclosure can access a basolateral compartment (e.g., Lamina propria) and/or the interior of an epithelial cell without damaging the cell or cell layer and without being altered, degraded or modified (e.g., chemically or enzymatically altered or modified). The carrier constructs (e.g., isolated delivery constructs) of the present disclosure can further utilize specific intracellular compartments during transcytosis and/or intracellular delivery to achieve the described transport efficiency.
The present disclosure provides methods and compositions that can comprise carriers that use (or interaction with) a set of endogenous proteins and receptors involved in the apical-to-basal transcytosis process across epithelial cells, such as polarized intestinal epithelial cells (e.g., enterocytes), to mediate transcytosis of a carrier coupled to a cargo from a lumen bordering the apical surface of a mucous membrane to the basolateral side of a mucous membrane. The delivery constructs disclosed herein can engage in interactions with such proteins and receptors to provide efficient transport and delivery of various cargo molecules to locations within an epithelial cell and/or across an epithelial cell to the basal side of an epithelium (e.g., a gut epithelium of a subject). The constructs described herein, such as delivery constructs, can comprise a carrier coupled to a heterologous cargo, wherein the carrier and/or the heterologous cargo can interact with proteins and/or receptors during intracellular delivery (e.g., to a supranuclear region or to a compartment located at the basal side within the epithelial cell) or during transcytosis (e.g., vesicular transcytosis). The carrier can interact with one or more proteins (e.g., receptors or enzymes). These interactions can be dynamical and/or pH-dependent. It is pointed out that the herein described interactions are examples only and are not limiting the methods and compositions of this disclosure to other interactions (e.g., with other proteins or receptors).
The compositions and methods disclosed herein provide efficient delivery and transport of various cargo molecules (e.g., small molecules as well as macromolecules) across epithelial cells and/or into epithelial cells. The carriers described herein achieve such efficient delivery of cargo in a manner that does not impair the epithelial cell barrier nor the delivery construct itself. Thus, the functional properties of the delivery constructs (e.g., those of the carrier as well as the functions of the cargo) can be retained during transport, allowing a fast and efficient delivery of such cargo. The presently described carriers utilize endogenous trafficking pathways to deliver exogenous or endogenous cargo molecules to specific locations. Those locations can be inside an epithelial cell and/or in basolateral compartments outside epithelial cells on the basal side, e.g., the Lamina propria.
The carriers of the present disclosure comprise can be derived from an exotoxin. Bacterial protein toxins are well known in the art, and are discussed in such sources as Burns, D., et al., eds., BACTERIAL PROTEIN TOXINS, ASM Press, Herndon Va. (2003), Aktories, K. and Just, I., eds., BACTERIAL PROTEIN TOXINS (HANDBOOK OF EXPERIMENTAL PHARMACOLOGY), Springer-Verlag, Berlin, Germany (2000), and Alouf, J. and Popoff, M., eds., THE COMPREHENSIVE SOURCEBOOK OF BACTERIAL PROTEIN TOXINS, Academic Press, Inc., San Diego, Calif. (3rd Ed., 2006).
As further described herein, an exotoxin can comprise one or more domains. As disclosed herein, an exotoxin can be Cholix or PE. For Cholix, the following nomenclature is used herein to describe its various domains (N- to C-terminus) and using the functional Cholix variant having the amino acid sequence set forth in SEQ ID NO: 1 as a reference sequence: (i) domain I (amino acid residues 1-265, SEQ ID NO: 4), (ii) domain II (amino acid residues 266-386, SEQ ID NO: 126), (iii) domain Ib (amino acid residues 387-425, SEQ ID NO: 127), and (iv) domain III (amino acid residues 426-634, SEQ ID NO: 128). For PE, the following nomenclature is used herein to describe its various domains (N- to C-terminus) and using the functional PE variant having the amino acid sequence set forth in SEQ ID NO: 135 as a reference sequence: (i) domain I (amino acid residues 1-252, SEQ ID NO: 137), (ii) domain II (amino acid residues 253-364, SEQ ID NO: 138), (iii) domain Ib (amino acid residues 365-404, SEQ ID NO: 139), and (iv) domain III (amino acid residues 405-613, SEQ ID NO: 140). Moreover, the ranges of amino acid residues defining these domains can be flexible and variations of about 5-10 amino acid residues may still fall within the scope of this disclosure, e.g., describing an amino acid sequence comprising the amino acid residues 5-265 or 5-270, or 1-260, or 5-260 of full-length Cholix may still be understood as a Cholix domain I and so forth. As disclosed herein, the terms “domain I” and “receptor binding domain” of an exotoxin can be used interchangeably. As disclosed herein, the terms “domain II” and “translocation domain” of an exotoxin can be used interchangeably. As disclosed herein, the terms “domain III”, “catalytic domain” and “cytotoxic domain” of an exotoxin can be used interchangeably.
Pseudomonas aeruginosa exotoxin A (PE), Corynebacterium diphtheria Diphtheria carrier (DT), and Vibrio cholera Cholix make up a family of bacterial protein toxins that act as ADP-ribosyltransferases. Thus, the carrier can be derived from a Cholix toxin. The carrier can be derived from a PE.
A Cholix polypeptide as described herein may be rendered non-toxic by one or more amino acid substitutions. A Cholix derived polypeptide or carrier as described herein may be rendered non-toxic by substituting a glutamic acid residue at position 581 of the amino acid sequence set forth in SEQ ID NO: 2 with alanine, resulting in a Cholix construct comprising an amino acid sequence set forth in SEQ ID NO: 3.
As further described herein, Cholix and PE are organized into distinct domains (I, II, Ib, and III) that are denoted based upon their structural relationships. Domain I appears to facilitate exotoxin internalization and transcytosis, whereas domains II, Ib, and III provide other functions as, for example, enzymatic activity in case of domain III that can ADP-ribosylate elongation factor 2 to induce cell apoptosis via blockade of protein synthesis. It has previously been unknown what components of PE and Cholix proteins are involved in the trans-epithelial transcytosis process.
Cholix is secreted by Vibrio cholera as a 70.7 kDa protein composed of three prominent globular domains (Ia, II, and III) and one small subdomain (Ib) connecting domains II and III similar to the structure of PE (Jorgensen, R. et al., J Biol Chem 283(16):10671-10678, 2008). Mature Cholix comprises a genus of functional variants, wherein each variant can differ in one or more amino acid residues compared to another variant. However, all Cholix variants disclosed herein and encompassed in this disclosure are functional Cholix variants. As used herein, Cholix is a 634-residue protein, and two functional variants are specifically included herein, which are those having the amino acid sequences set forth in SEQ ID NO: 1 and SEQ ID NO: 1. A nucleic acid encoding the mature Cholix as used herein is set forth in SEQ ID NO: 134.
Pseudomonas exotoxin A or “PE” is secreted by Pseudomonas aeruginosa as a 67 kDa protein composed of three prominent globular domains (Ia, II, and III) and one small subdomain (Ib) connecting domains II and III (see Allured et. al., Proc. Natl. Acad. Sci. 83:1320 1324, 1986). Mature PE as used herein is a 613-residue protein, whose sequence is set forth in SEQ ID NO: 134. A nucleic acid encoding mature PE as used herein is set forth in SEQ ID NO: 135.
The amino acid sequence of the mature Cholix toxin is set forth in SEQ ID NO: 1 and is used as the reference sequence, unless specified otherwise. For example, the amino acid sequence set forth in SEQ ID NO: 4 contains the amino acid residues 1-265 of the amino acid sequence of mature Cholix toxin set forth in SEQ ID NO: 1 and is defined as Cholix domain I. Thus, the polypeptide having the amino acid sequence set forth in SEQ ID NO: 4 can also be described as “Chx1-265” (or “Cholix1-265” or “Cholix265” or “Cholix domain I”). In addition to the Cholix reference sequence set forth in SEQ ID NO: 1, any other, functionally active, Cholix exotoxin variants are encompassed in the present disclosure, e.g., those that comprise a consensus sequence defining the functional activity of the Cholix exotoxins. (See e.g., Awasthi et al. Novel Cholix toxin variants, ADP-ribosylating toxins in Vibrio Cholerae Non-O1/Non-O139 strains, and their pathogenicity, Infection and Immunity, 81(2), p. 531-541 (2013)). As an example, the polypeptide having the amino acid sequence set forth in SEQ ID NO: 2 is a functional variant of SEQ ID NO: 1. As such, a domain I derived from that Cholix exotoxin sequence, or a truncated version thereof, can be used as a carrier for the rapid and efficient delivery of cargo. Using the nomenclature described herein with the reference sequence being SEQ ID NO: 1, a domain I polypeptide of the Cholix exotoxin with SEQ ID NO: 2 can also be described as amino acid residues 14 of SEQ ID NO: 2+Cholix5-265.
In other cases, and as described herein, a first carrier and a second carrier are produced in a different expression system (e.g., a bacterial or a mammalian expression system). Bacterial expression systems include E. coli, and mammalian expression systems include CHO cells, for example. A bacterially produced polypeptide can comprise an N-cap, wherein the N-cap can comprise one more modifications at the N-terminal of the polypeptide. An N-cap can comprise an N-terminal methionine residue. Examples of Cholix domain I derived carrier polypeptides that can be bacterially produced and that comprise such N-terminal methionine include those comprising the amino acid sequences set forth in SEQ ID NO: 5, SEQ ID NO: 7, SEQ ID NO: 9, SEQ ID NO: 11, SEQ ID NO: 31, SEQ ID NO: 107, and SEQ ID NO: 125.
The present disclosure contemplates isolated non-naturally occurring and bacterial toxin derived carriers (e.g., an exotoxin derived) that can be coupled to a cargo (e.g., a biologically active); wherein the carrier is capable of delivering the cargo (e.g., a biologically active) via transcytosis transport across the intestinal epithelium. The carrier can be derived from a domain I of an exotoxin (e.g., Cholix or PE). A carrier that is derived form a domain I of an exotoxin can lack a domain II (e.g., SEQ ID NO: 126 or SEQ ID NO: 138), a domain Ib (e.g., SEQ ID NO: 127 or SEQ ID NO: 139), or a domain III (e.g., SEQ ID NO: 128 or SEQ ID NO: 140) of an exotoxin (e.g., Cholix or PE).
As described herein, a carrier that “lacks” a domain II, domain Ib, and a domain III of an exotoxin (e.g., Cholix and/or PE) can still comprise a portion of the domain II, a domain Ib, or the domain III of the exotoxin, or a combination thereof. Thus, the term “lacking” as referred to herein means that a carrier does not comprise a complete domain II, a complete domain Ib, or a complete domain III. A carrier can comprise no more than 70% of the amino acid residues of a domain II, a domain Ib, or a domain III of an exotoxin. For example, a carrier can comprise a Cholix domain I (e.g., SEQ ID NO: 4 or SEQ ID NO: 5) or a truncated version thereof, and further comprise the amino acid residues 1-82 of Cholix domain II (SEQ ID NO: 126). A carrier can comprise no more than 60% of the amino acid residues of a domain II, a domain Ib, or a domain III of an exotoxin. A carrier can comprise no more than 50% of the amino acid residues of a domain II, a domain Ib, or a domain III of an exotoxin. A carrier can comprise no more than 25% of the amino acid residues of a domain II, a domain Ib, or a domain III of an exotoxin. A carrier can comprise no more than 10% of the amino acid residues of a domain II, a domain Ib, or a domain III of an exotoxin.
The present disclosure contemplates isolated non-naturally occurring and bacterial toxin derived carriers (e.g., an exotoxin derived) that can be coupled to a cargo (e.g., a biologically active); wherein the carrier is capable of delivering the cargo (e.g., a biologically active) to the interior of an epithelial cell, such as an intracellular vesicle or compartment or the cytosol. Regions and/or compartments in the interior of an epithelial cell can include regions and/or compartments on the apical side of the interior of an epithelial cell, regions and/or compartments on the basal side of the interior of an epithelial cell, supranuclear regions of an epithelial cell, or any combination thereof. The epithelial cell can be a polarized gut epithelial cell. The polarized gut epithelial cell can be part of a polarized epithelial cell monolayer (e.g., comprising Caco-2 cells) or it can be part of a gut epithelium of a subject (e.g., a rodent or a human).
A carrier can be derived from a bacterial carrier such as an exotoxin (e.g., Cholix and/or PE) and can be derived from a domain I of said exotoxin and can lack a domain II (e.g., SEQ ID NO: 126 or SEQ ID NO: 138), a domain Ib (e.g., SEQ ID NO: 127 or SEQ ID NO: 139), or a domain III (e.g., SEQ ID NO: 128 or SEQ ID NO: 140) of an exotoxin (e.g., Cholix or PE). The carrier can comprise a receptor binding domain or binding fragment, which can be a domain, region, or fragment within the exotoxin derived domain I, and which allows binding of the delivery construct to one or more selective or non-selective receptors on the luminal surface of an epithelial cell. A receptor can be a selective receptor or a non-selective receptor, such as a non-selective scavenger receptor on the luminal surface of intestinal epithelial cells. The one or more receptors that a carrier can interact with on the surface of an epithelial cell and/or during endocytosis can include a low density lipoprotein receptor-related protein 1 (LRP1) or a transmembrane protein 132 (TMEM132). Thus, the delivery construct can bind to one or more cell surface receptor that can be present on the apical membrane of an epithelial cell with sufficient affinity to allow endocytosis. The delivery construct can bind to any receptor known to be present on the apical membrane of an epithelial cell by one of skill in the art without limitation. The carrier can bind to LRP1. The carrier can bind to TMEM132. Alternatively, the carrier can bind to LRP1 and TMEM132.
A carrier can be derived from a domain I of an exotoxin. The exotoxin is selected from the group consisting of Cholix and PE. A carrier as described herein is derived from a domain I of an exotoxin, wherein the exotoxin is Cholix. Thus, a carrier as described herein can comprise an amino acid sequence that is derived from that of Cholix domain I (e.g., SEQ ID NO: 4 or SEQ ID NO: 5). A Cholix Domain I (e.g., SEQ ID NO: 4) can comprise amino acids 1-265 of SEQ ID NO: 1 or it can comprise amino acid sequence set forth in SEQ ID NO: 5 (e.g., when bacterially produced comprising an N-terminal methionine residue) and can be described as a “receptor binding domain” that functions as a ligand for a cell surface receptor and mediates Cholix binding and endocytosis. A carrier can comprise an amino acid sequence with greater than 50% homology to any one of SEQ ID NO: 4-SEQ ID NO: 125. A carrier can comprise an amino acid sequence with greater than 60% homology to any one of SEQ ID NO: 4-SEQ ID NO: 125. A carrier can comprise an amino acid sequence with greater than 70% homology to any one of SEQ ID NO: 4-SEQ ID NO: 125. A carrier can comprise an amino acid sequence with greater than 80% homology to any one of SEQ ID NO: 4-SEQ ID NO: 125. A carrier can comprise an amino acid sequence with greater than 90% homology to any one of SEQ ID NO: 4-SEQ ID NO: 125. A carrier can comprise an amino acid sequence with greater than 95% homology to any one of SEQ ID NO: 4-SEQ ID NO: 125. Conservative or non-conservative substitutions can be made to an amino acid sequence of any one of SEQ ID NO: 4-SEQ ID NO: 125. As described herein, an amino acid residue substitution will be identified by reference to the particular amino acid substitution at a specific amino acid residue. Thus, e.g., the term “S30A” indicates that the “S” (serine, in standard single letter code) residue at position 30 in SEQ ID NO: 4 has been substituted with an “A” (alanine, in standard single letter code), and the modified carrier will be identified as “CholixS30A”. A carrier can be a truncated version of a Cholix domain I sequence set forth in SEQ ID NO: 4 or SEQ ID NO: 5. Thus, a carrier comprising a truncated version of a Cholix domain I can comprise an amino acid sequence set forth in any one of SEQ ID NO: 6-SEQ ID NO: 125. A carrier can comprise an amino acid sequence of any one of SEQ ID NO: 4-SEQ ID NO: 125, wherein one or more amino residues of such sequence is deleted. A carrier can comprise an amino acid sequence of any one of SEQ ID NO: 4-SEQ ID NO: 125, wherein one or more amino acid residues can be substituted with another amino acid. As described herein, a truncated carrier can be identified by reference to the amino acid residues comprising the truncated toxin, e.g., a truncated Cholix carrier consisting of amino acid residues 1-260 of SEQ ID NO: 4 will be identified as Cholix260 and so forth, according to nomenclature described herein.
Exemplary nucleotide and amino acid sequences of carriers as described herein are shown below in TABLE 2. In various embodiments, a carrier comprises any of the amino acid sequences shown in TABLE 2, or fragment, or a combination thereof.
A carrier can be a polypeptide that is derived from a Cholix exotoxin and having: at most 5 amino acid residues; at most 10 amino acid residues; at most 15 amino acid residues; at most 20 amino acid residues; at most 30 amino acid residues; at most 40 amino acid residues; at most 50 amino acid residues; at most 60 amino acid residues; at most 70 amino acid residues; at most 80 amino acid residues; at most 90 amino acid residues; at most 100 amino acid residues; at most 110 amino acid residues; at most 120 amino acid residues; at most 130 amino acid residues; at most 140 amino acid residues; at most 150 amino acid residues; at most 160 amino acid residues; at most 170 amino acid residues; at most 180 amino acid residues; at most 190 amino acid residues; at most 200 amino acid residues; at most 210 amino acid residues; at most 220 amino acid residues; at most 230 amino acid residues; at most 240 amino acid residues; at most 250 amino acid residues; at most 260 amino acid residues; and at most 265 amino acid residues of SEQ ID NO: 4 or SEQ ID NO: 5. The bacterial carrier receptor binding domain can be a polypeptide derived from Cholix and having at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 99%, or more sequence homology with SEQ ID NO: 4 or SEQ ID NO: 5. The carrier can be a polypeptide derived from Cholix and having at most 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, or 99% sequence homology with any one of SEQ ID NO: 1-SEQ ID NO: 133. The amino acid residues can be consecutive. The amino acid residues are also be non-consecutive. A carrier can be derived from a domain I of a Cholix exotoxin. A carrier that is derived from a domain I of an exotoxin can comprise an amino acid having at least 80% sequence identity to any one of the amino acid sequences set forth in SEQ ID NO: 4-SEQ ID NO: 125, or at least 80% sequence identity to a functional fragment thereof. A carrier that is derived from a domain I of an exotoxin can comprise an amino acid having at least 90% sequence identity to any one of the amino acid sequences set forth in SEQ ID NO: 4-SEQ ID NO: 125, or at least 90% sequence identity to a functional fragment thereof. A carrier that is derived from a domain I of an exotoxin can comprise an amino acid having at least 95% sequence identity to any one of the amino acid sequences set forth in SEQ ID NO: 4-SEQ ID NO: 125, or at least 95% sequence identity to a functional fragment thereof. A carrier that is derived from a domain I of an exotoxin can comprise an amino acid having at least 99% sequence identity to any one of the amino acid sequences set forth in SEQ ID NO: 4-SEQ ID NO: 125, or at least 99% sequence identity to a functional fragment thereof. A carrier that is derived from a domain I of an exotoxin can comprise an amino acid having 100% sequence identity to any one of the amino acid sequences set forth in SEQ ID NO: 4-SEQ ID NO: 125, or 100% sequence identity to a functional fragment thereof.
A carrier can be artificially synthesized. A carrier can be an artificially synthesized polypeptide having at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 99%, or more amino acid sequence homology to a Cholix domain I (e.g., any one of SEQ ID NO: 4-SEQ ID NO: 125). A carrier can be a synthetic polypeptide having at most 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, or 99% amino acid sequence homology to a Cholix domain I (e.g., any one of SEQ ID NO: 4-SEQ ID NO: 125). The polypeptide that a carrier can be comprises of can be synthesized using solid-phase synthesis.
A carrier can be a polypeptide derived from Cholix and having at most 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, or 99% sequence homology with any one of SEQ ID NO: 4-SEQ ID NO: 125. Certain fragments within the amino acid sequence of the carrier can have specific functions that can be related to one or more aspects of the transcytosis process. These functions can comprise crossing a polarized monolayer of primary human small intestinal epithelial cells or an intact gut epithelium, enabling or promoting endocytosis into an epithelial cell, apical-to-basal transport, release of the delivery construct from the basal membrane into a basolateral compartment, delivery into an intracellular vesicle or compartment or the cytosol of an epithelial cell, and/or delivery to a supranuclear region of an epithelial cell (e.g., a polarized gut epithelial cell).
Thus, the present disclosure provides carriers that can have various functions (e.g., one or more of endocytosis, transcytosis, intracellular delivery, etc.). Such a carrier can comprise an amino acid sequence having at least 80% sequence identity to the amino acid sequence of SEQ ID NO: 4 or SEQ ID NO: 5 or at least 80% sequence identity to a functional fragment thereof, and no more than 347 contiguous amino acid residues from SEQ ID NO: 1. Such a carrier can comprise a deletion or mutation in one or more of amino acid residues of the amino acid sequence set forth in SEQ ID NO: 4 (e.g., a Cholix domain I expressed in a mammalian cell) or SEQ ID NO: 5 (e.g., a Cholix domain I expressed in a bacterial cell). Such a carrier can comprise an amino acid sequence having at least 90% sequence identity to the amino acid sequence of SEQ ID NO: 4 or SEQ ID NO: 5 or at least 90% sequence identity to a functional fragment thereof, and no more than 347 contiguous amino acid residues from SEQ ID NO: 1. A carrier can comprise an amino acid sequence having at least 95% sequence identity to the amino acid sequence of SEQ ID NO: 4 or SEQ ID NO: 5 or at least 95% sequence identity to a functional fragment thereof, and no more than 347 contiguous amino acid residues from SEQ ID NO: 1. A carrier can comprise an amino acid sequence having at least 99% sequence identity to the amino acid sequence of SEQ ID NO: 4 or SEQ ID NO: 5 or at least 99% sequence identity to a functional fragment thereof, and no more than 347 contiguous amino acid residues from SEQ ID NO: 1. A carrier can comprise an amino acid sequence having 100% sequence identity to the amino acid sequence of SEQ ID NO: 4 or SEQ ID NO: 5 or 100% sequence identity to a functional fragment thereof, and no more than 347 contiguous amino acid residues from SEQ ID NO: 1. A carrier disclosed herein can comprise the amino acid sequence set forth in SEQ ID NO: 4 or SEQ ID NO: 5 or a functional fragment thereof. The carrier can comprises the amino acid sequence set forth in SEQ ID NO: 6 or SEQ ID NO: 7 or a functional fragment thereof. The carrier can comprises the amino acid sequence set forth in SEQ ID NO: 8 or SEQ ID NO: 9 or a functional fragment thereof.
A functional carrier of the present disclosure can comprise an amino acid sequence having at least 80% sequence identity to any one of the amino acid sequences set forth in SEQ ID NO: 148, SEQ ID NO: 149, SEQ ID NO: 150, SEQ ID NO: 151, SEQ ID NO: 152, a functional fragment thereof, or any combination thereof. A carrier can comprise an amino acid sequence having at least 90% sequence identity to any one of the amino acid sequences set forth in SEQ ID NO: 148, SEQ ID NO: 149, SEQ ID NO: 150, SEQ ID NO: 151, SEQ ID NO: 152, a functional fragment thereof, or any combination thereof. A carrier can comprise an amino acid sequence having at least 95% sequence identity to any one of the amino acid sequences set forth in SEQ ID NO: 148, SEQ ID NO: 149, SEQ ID NO: 150, SEQ ID NO: 151, SEQ ID NO: 152, a functional fragment thereof, or any combination thereof. A carrier can comprise comprises an amino acid sequence having at least 99% sequence identity to any one of the amino acid sequences set forth in SEQ ID NO: 148, SEQ ID NO: 149, SEQ ID NO: 150, SEQ ID NO: 151, SEQ ID NO: 152, a functional fragment thereof, or any combination thereof. A carrier can comprise a spatial structure in which one or more amino acid residues of SEQ ID NO: 148 or SEQ ID NO: 149 are in close proximity to one or more amino acid residues of SEQ ID NO: 151, and one or more amino acid residues of SEQ ID NO: 148 or SEQ ID NO: 149 are in close proximity to one or more amino acid residues of SEQ ID NO: 152.
A carrier of the present disclosure can be capable of delivering a cargo across an epithelial cell (e.g., a polarized epithelial cell). Such a carrier can comprise an amino acid sequence having at least 80% sequence identity to the amino acid sequence set forth in SEQ ID NO: 30 or SEQ ID NO: 31 or the amino acid sequence set forth in SEQ ID NO: 10 or SEQ ID NO: 11 or at least 80% sequence identity to a functional fragment thereof. A carrier can comprise an amino acid sequence having at least 90% sequence identity to the amino acid sequence set forth in SEQ ID NO: 30 or SEQ ID NO: 31 or the amino acid sequence set forth in SEQ ID NO: 10 or SEQ ID NO: 11 or at least 90% sequence identity to a functional fragment thereof. A carrier can comprise an amino acid sequence having at least 95% sequence identity to the amino acid sequence set forth in SEQ ID NO: 30 or SEQ ID NO: 31 or the amino acid sequence set forth in SEQ ID NO: 10 or SEQ ID NO: 11 or at least 95% sequence identity to a functional fragment thereof. A carrier can comprise an amino acid sequence having at least 99% sequence identity to the amino acid sequence set forth in SEQ ID NO: 30 or SEQ ID NO: 31 or the amino acid sequence set forth in SEQ ID NO: 10 or SEQ ID NO: 11 or at least 99% sequence identity to a functional fragment thereof. A carrier can further comprise a deletion or mutation in one or more of amino acid residues 1-187 or 1-205 of SEQ ID NO: 10 or 1-186 or 1-206 of SEQ ID NO: 11. A carrier can comprise residues 1-186 of SEQ ID NO: 30 or 1-187 of SEQ ID NO: 31 and no more than 206 contiguous amino acid residues of SEQ ID NO: 1.
The methods and compositions of the present disclosure can comprise a carrier comprising an amino acid sequence having at least 80% sequence identity to the amino acid sequence set forth in any one of SEQ ID NO: 10-SEQ ID NO: 31 or at least 80% sequence identity to a functional fragment thereof. A carrier can comprise an amino acid sequence having at least 90% sequence identity to the amino acid sequence set forth in any one of SEQ ID NO: 10-SEQ ID NO: 31 or at least 90% sequence identity to a functional fragment thereof. In some instances, the carrier comprises an amino acid sequence having at least 95% sequence identity to the amino acid sequence set forth in any one of SEQ ID NO: 10-SEQ ID NO: 31 or at least 95% sequence identity to a functional fragment thereof. A carrier can comprise an amino acid sequence having at least 99% sequence identity to the amino acid sequence set forth in any one of SEQ ID NO: 10-SEQ ID NO: 31 or at least 99% sequence identity to a functional fragment thereof. The carrier can comprises the amino acid sequence set forth in SEQ ID NO: 10 or SEQ ID NO: 11 or a functional fragment thereof.
A carrier can comprise an amino acid sequence having at least 80% sequence identity to the amino acid sequence set forth in SEQ ID NO: 106 or SEQ ID NO: 107 or to the amino acid sequence set forth in SEQ ID NO: 30 or SEQ ID NO: 31 or at least 80% sequence identity to a functional fragment thereof. Such a carrier can be capable of delivering cargo to an intracellular location. Such an intracellular location may be a supranuclear region. Such a carrier can comprise an amino acid sequence having at least 90% sequence identity to the amino acid sequence set forth in SEQ ID NO: 106 or SEQ ID NO: 107 or to the amino acid sequence set forth in SEQ ID NO: 30 or SEQ ID NO: 31 or at least 90% sequence identity to a functional fragment thereof. A carrier can comprise an amino acid sequence having at least 95% sequence identity to the amino acid sequence set forth in SEQ ID NO: 106 or SEQ ID NO: 107 or to the amino acid sequence set forth in SEQ ID NO: 30 or SEQ ID NO: 31 or at least 95% sequence identity to a functional fragment thereof. A carrier can comprise an amino acid sequence having at least 99% sequence identity to the amino acid sequence set forth in SEQ ID NO: 106 or SEQ ID NO: 107 or to the amino acid sequence set forth in SEQ ID NO: 30 or SEQ ID NO: 31 or at least 99% sequence identity to a functional fragment thereof. A carrier can comprise a deletion or mutation in one or more of amino acid residues 1-151 or 1-187 of SEQ ID NO: 4 or SEQ ID NO: 5.
The methods and compositions of the present disclosure provide a carrier that can lack any one or more of the amino acid residues 1-39 of SEQ ID NO: 5 or amino acid residues 1-38 of SEQ ID NO: 4. Such a carrier can be capable of delivering cargo to an intracellular location via endocytosis. Such a location can be an apical region or compartment. A carrier can lack all of the amino acid residues 1-39 of SEQ ID NO: 5 or amino acid residues 1-38 of SEQ ID NO: 4. A carrier can comprises an amino acid sequence having at least 80% sequence identity to the amino acid sequence set forth in SEQ ID NO: 70 or 80% sequence identity to a functional fragment thereof. A carrier can comprises an amino acid sequence having at least 90% sequence identity to the amino acid sequence set forth in SEQ ID NO: 70 or 90% sequence identity to a functional fragment thereof. A carrier can comprises an amino acid sequence having at least 95% sequence identity to the amino acid sequence set forth in SEQ ID NO: 70 or 95% sequence identity to a functional fragment thereof. A carrier can comprises an amino acid sequence having at least 99% sequence identity to the amino acid sequence set forth in SEQ ID NO: 70 or 99% sequence identity to a functional fragment thereof. A carrier can comprises residues 1-151 of SEQ ID NO: 5 or residues 1-150 of SEQ ID NO: 4 and no more than 187 contiguous amino acid residues of SEQ ID NO: 1.
A carrier of the present disclosure can comprise a truncated version of a Cholix domain I. Thus, a carrier can comprise an amino acid sequence having at least 80% sequence identity to the amino acid sequence set forth in any one of SEQ ID NO: 30-SEQ ID NO: 107 or at least 80% sequence identity to a functional fragment thereof. Such a carrier can be capable of delivering cargo to an intracellular location via endocytosis. Such a location can be an apical and/or a basal region or compartment. A carrier can comprise an amino acid sequence having at least 90% sequence identity to the amino acid sequence set forth in any one of SEQ ID NO: 30-SEQ ID NO: 107 or at least 90% sequence identity to a functional fragment thereof. A carrier can comprise an amino acid sequence having at least 95% sequence identity to the amino acid sequence set forth in any one of SEQ ID NO: 30-SEQ ID NO: 107 or at least 95% sequence identity to a functional fragment thereof. A carrier can comprise an amino acid sequence having at least 99% sequence identity to the amino acid sequence set forth in any one of SEQ ID NO: 30-SEQ ID NO: 107 or at least 99% sequence identity to a functional fragment thereof. A carrier can comprise the amino acid sequence set forth in SEQ ID NO: 30 or SEQ ID NO: 31 or a functional fragment thereof.
A carrier of the present disclosure can comprises an amino acid sequence having at least 80% sequence identity to the amino acid sequence set forth in SEQ ID NO: 106 or SEQ ID NO: 107 or the amino acid sequence set forth in SEQ ID NO: 124 or SEQ ID NO: 125 or at least 80% sequence identity to a functional fragment thereof. Such a carrier can be capable of delivering cargo to an intracellular location via endocytosis. Such a location can be an apical region or compartment. A carrier can comprise an amino acid sequence having at least 90% sequence identity to the amino acid sequence set forth in SEQ ID NO: 106 or SEQ ID NO: 107 or the amino acid sequence set forth in SEQ ID NO: 124 or SEQ ID NO: 125 or at least 90% sequence identity to a functional fragment thereof. A carrier can comprise an amino acid sequence having at least 95% sequence identity to the amino acid sequence set forth in SEQ ID NO: 106 or SEQ ID NO: 107 or the amino acid sequence set forth in SEQ ID NO: 124 or SEQ ID NO: 125 or at least 95% sequence identity to a functional fragment thereof. A carrier can comprise an amino acid sequence having at least 99% sequence identity to the amino acid sequence set forth in SEQ ID NO: 106 or SEQ ID NO: 107 or the amino acid sequence set forth in SEQ ID NO: 124 or SEQ ID NO: 125 or at least 99% sequence identity to a functional fragment thereof. A carrier can further comprise a deletion or mutation in one or more of amino acid residues 1-151 of SEQ ID NO: 6 or in one or more of amino acid residues 1-150 of SEQ ID NO: 7. A carrier as described herein can comprise residues 1-134 of SEQ ID NO: 5 or residues 1-133 of SEQ ID NO: 4 and no more than 151 contiguous amino acid residues of SEQ ID NO: 1. A carrier can comprise an amino acid sequence having at least 80% sequence identity to the amino acid sequence set forth in any of SEQ ID NO: 106-SEQ ID NO: 125 or at least 80% sequence identity to a functional fragment thereof. A carrier can comprise an amino acid sequence having at least 90% sequence identity to the amino acid sequence set forth in any of SEQ ID NO: 106-SEQ ID NO: 125 or at least 90% sequence identity to a functional fragment thereof. A carrier can comprise an amino acid sequence having at least 95% sequence identity to the amino acid sequence set forth in any of SEQ ID NO: 106-SEQ ID NO: 125 or at least 95% sequence identity to a functional fragment thereof. A carrier can comprise an amino acid sequence having at least 99% sequence identity to the amino acid sequence set forth in any of SEQ ID NO: 106-SEQ ID NO: 125 or at least 99% sequence identity to a functional fragment thereof. A carrier can comprise the amino acid sequence set forth in SEQ ID NO: 106 or SEQ ID NO: 107 or a functional fragment thereof.
A carrier of the present disclosure can be derived from a domain I of an exotoxin. The exotoxin can be Cholix. A carrier that is derived from a Cholix domain I can comprise at least one but no more than 20 beta strands. A carrier that is derived from a Cholix domain I can comprise at least one but no more than 15 beta strands. A carrier that is derived from a Cholix domain I can comprise between 10 and 15 beta strands. A carrier that is derived from a Cholix domain I can comprise at least one but less than 10 α-helices. A carrier that is derived from a Cholix domain I can comprise between 1 and 5 α-helices.
A carrier of the present disclosure can comprise an amino acid fragment of Cholix domain I that can enable, promote, and/or enhance apical entry of the Cholix derived carrier into epithelial cells such as polarized gut epithelial cells. Such a fragment can comprise the amino acid sequence set forth in SEQ ID NO: 148 and can promote and/or enhance apical entry of the Cholix derived carrier into epithelial cells on the apical epithelial/luminal surface. This may enhance the delivery and/or transport function of the carrier and increase the amount cargo molecules delivered and/or transported into and/or across an epithelial cell.
A carrier of the present disclosure can comprise an amino acid fragment of Cholix domain I that can enable, promote, and/or enhance apical-to-basal transcytosis of a Cholix-derived carrier as described herein. Such an amino acid fragment that enables, promotes, and/or enhances apical-to-basal transcytosis of the delivery construct can comprise an amino acid sequence set forth in SEQ ID NO: 149 or SEQ ID NO: 150. This may enhance the delivery and/or transport function of the carrier and increase the amount cargo molecules delivered and/or transported into and/or across an epithelial cell. For example, a carrier comprising such fragment with SEQ ID NO: 149 or SEQ ID NO: 150 can increase the amount cargo molecules delivered and/or transported to a basal compartment. This may further enhance basal release of the carrier.
A carrier of the present disclosure can comprise an amino acid fragment of Cholix domain I that can enable, promote, and/or enhance early and/or late endosomal sorting, thereby enabling, promoting, and/or enhancing transport of the Cholix-derived carrier to a supranuclear region within an epithelial cell. Such a peptide fragment of Cholix domain I comprising the amino acid sequence set forth in SEQ ID NO: 151 and can enable, promote, and/or enhance early endosomal sorting of a Cholix-derived delivery construct as described herein. Supranuclear regions that may be targeted using such a carrier can include the endoplasmatic reticulum, the Golgi apparatus, and/or endosomes. Thus, a carrier capable of accessing such region can provide efficient delivery of cargo to such regions.
A carrier of the present disclosure can comprise an amino acid fragment of Cholix domain I that can enable, promote, and/or enhance complete transcytosis of the Cholix-derived delivery construct across an intact epithelial layer such as the gut epithelium. Such a fragment comprising the amino acid sequence set forth in SEQ ID NO: 152 can enable, promote, and/or enhance complete transcytosis of the Cholix-derived delivery construct by enabling basal release of the carrier and/or the delivery construct from the epithelial cell. Complete transcytosis of the Cholix-derived delivery construct can be determined, for example, by measuring the presence of the delivery construct in a basolateral compartment or the Lamina propia. The ability of such carriers to delivery cargo across intact epithelial cell layers can be of high significance as it allows the oral administration of drugs that would not be able to cross such epithelial layers by themselves.
As described herein, the present disclosure contemplates the surprising finding that a carrier that is derived from a Cholix domain I and that lacks a Cholix domain II, domain Ib, and domain III, is sufficient for rapid and efficient apical-to-basal transcytosis (e.g., and sufficient for rapid and efficient apical-to-basal transport of cargo via transcytosis). Furthermore, it is shown that certain portions of the amino acid sequence of Cholix domain I can have specific functions related to apical-to-basal transcytosis across an epithelial cell, and/or the delivery into the cytosol or interior of an epithelial cell. A carrier of the present disclosure can comprise any one of the amino acid sequences set forth in SEQ ID NO: 4-SEQ ID NO: 125. A carrier of the present disclosure can comprise one or more of the functional amino acid peptide fragments of a Cholix domain I set forth in SEQ ID NO: 148-SEQ ID NO: 152. A carrier of the present disclosure can comprise a Cholix domain I with an amino acid sequence set forth in SEQ ID NO: 4 and/or SEQ ID NO: 5.
The present disclosure further contemplates carriers that comprise one or more functional fragments of a Cholix domain I. The functional fragments can be in the same order as in the mature Cholix amino acid sequence, or the functional fragments can be in a different order without impairing the functions(s) of such functional fragments. Thus, a carrier can comprise one or more of the functional amino acid sequences derived a Cholix domain I and set forth in SEQ ID NO: 148-SEQ ID NO: 152. Such amino acid sequences can be linked together to form a polymeric polypeptide comprising a plurality of Cholix domain I derived peptide fragments. Such a carrier of the present disclosure can comprise one or more amino acid sequences set forth in SEQ ID NO: 148-SEQ ID NO: 152, or any combination thereof, that form a polymeric polypeptide capable of efficient transcytosis across epithelial layers such as the gut epithelium. Such a polymeric peptide can comprise a plurality of amino acid fragment derived from Cholix domain I and such polymeric polypeptide can be used instead of and/or in addition to a Cholix domain I polypeptide or a truncated version thereof. Such a non-naturally occurring synthetic polymeric peptide can possess superior or inferior transcytosis capabilities when used as a delivery construct compared to Cholix domain I or a truncated version thereof. The functionality of such synthetic polypeptides can depend on several factors such spatial structure and geometry, stability, and/or the cargo that may be coupled to such polypeptide.
A carrier of the present disclosure may not be significantly altered in a chemical, structural, and/or conformational manner during the transcytosis process across an epithelial cell. Thus, the Cholix toxin-derived carrier as disclosed herein (including polymeric peptides comprising a plurality of Cholix-derived amino acid fragments) can be used as an efficient delivery vehicle for various cargo molecules (e.g., therapeutic cargo molecules) as described herein. A Cholix-derived carrier as described herein does not contain the domains II and III, but instead is attached to one or more cargo moieties (e.g., therapeutic cargo molecules) without having reduced transport and/or transcytosis capabilities compared to mature ntChx.
Transport of a carrier as described herein across an epithelial layer (e.g., a gut epithelium) can comprise multiple steps. Transport of a delivery construct (e.g., a Cholix-derived delivery construct) can comprise elements of Cholix domain I functioning in a multistep process. For example, transport or transcytosis can include apical endocytosis, vesicular trafficking involving apical, basal, and/or supra-nuclear regions of enterocytes, and release from the basal membrane to reach the Lamina propria. Furthermore, a Cholix-derived delivery construct as described herein can utilize a receptor-mediated-type endocytosis process. Receptor-mediated endocytosis can involve an amino acid sequence having at least 80% sequence identity to the amino acid set forth in SEQ ID NO: 148 or a fragment or derivative thereof, which, can provide access to an early endosomal vesicular compartment in the apical portion of enterocytes, e.g., via endocytosis. An amino acid sequence having at least 80% sequence identity to the amino acid set forth in SEQ ID NO: 151 or a fragment or derivative thereof, can allow, promote, or enhance the movement of a Cholix-derived delivery construct to a supranuclear region consistent with a sorting site in the cell for secretory events. Movement of a delivery construct comprising a Cholix-derived carrier to the basal compartment of the cells can be more efficient when the carrier comprises an amino acid sequence having at least 80% sequence identity to the amino acid set forth in SEQ ID NO: 149 or SEQ ID NO: 150, or a fragment or derivative thereof. An amino acid sequence having at least 80% sequence identity to the amino acid set forth in SEQ ID NO: 149, a fragment or derivative thereof, can provide a mechanism for secretion from the basal membrane that releases an intact and functional delivery construct (e.g., including the cargo moiety) into a basolateral compartment or the Lamina propria from where it can reach various other locations (e.g., cells, tissues or organs) within an organism (e.g., in a human or in a rodent).
In addition to leaving the carrier unaltered or unmodified during transcytosis, transport of a delivery construct as disclosed herein across an epithelial barrier (e.g., an intact intestinal epithelium) generally does not involve enterocyte intoxication or disruption. Thus, a delivery construct as disclosed herein can comprise a Cholix domain I, a fragment or truncated version thereof (e.g., any one of SEQ ID NO: 6-SEQ ID NO: 125), or a polymeric peptide comprising a plurality of amino acid fragments derived from a Cholix domain I (e.g., SEQ ID NO: 148-SEQ ID NO: 152), and wherein the other domains (e.g., domains II, domain Ib, and III) can be replaced by various other moieties, such as spacers, heterologous cargos (e.g., therapeutic and/or biologically active cargo), small molecules, nucleic acids (e.g., aptamers or interfering RNAs), or any combination thereof, as further described herein.
A carrier of the present disclosure can be used to deliver various cargo molecules into and/or across epithelial cells in an efficient manner, e.g., when comprising an amino acid sequence having at least 80% sequence identity to an amino acid sequence set forth in any one of SEQ ID NO: 4-SEQ ID NO: 125). Thus, a carrier of the present disclosure can enable efficient endocytosis on the apical site and transport into the interior of an epithelial cell (e.g., an enterocyte and/or a polarized gut epithelial cell) such as an intracellular vesicle or compartment or the cytosol and/or a supranuclear region. Such a carrier can comprise an amino acid sequence set forth in any one of SEQ ID NO: 30-SEQ ID NO: 125. Thus, constructs for delivery of cargo molecules into epithelial cells may comprise a truncated Cholix domain I or fragment of a Cholix domain I that does not comprise the amino acid sequence set forth in SEQ ID NO: 151, and/or the amino acid amino acid sequence set forth in SEQ ID NO: 152, or any combination thereof.
A carrier of the present disclosure can comprise one or more potential glycosylation sites. The one or more glycosylation sites can be located within a Cholix domain I (e.g., SEQ ID NO: 4 or SEQ ID NO: 5). A carrier as described herein can comprise the amino acid sequence set forth in SEQ ID NO: 5, wherein the asparagine residues N98, N154, N165, N224, or any combination thereof, can be potential glycosylation sites. Variation or mutation of one or more of these amino acid residues that can act as glycosylation sites can affect or reduce a function related to transcytosis of a delivery construct. TABLE 3 shows exemplary functional peptide fragments of Cholix domain I that were identified to provide one or more functions related to apical-to-basal transcytosis.
As further described herein, a carrier of the present disclosure can comprise one or more functional fragments. Such functional fragments can include those listed in TABLE 3. Thus, a carrier can comprise an amino acid sequence having at least 80% sequence identity to one or more of the amino acid sequences set forth in SEQ ID NO: 148-SEQ ID NO: 152. A carrier can comprise an amino acid sequence having at least 90% sequence identity to one or more of the amino acid sequences set forth in SEQ ID NO: 148-SEQ ID NO: 152. A carrier can comprise an amino acid sequence having at least 95% sequence identity to one or more of the amino acid sequences set forth in SEQ ID NO: 148-SEQ ID NO: 152. A carrier can comprise an amino acid sequence having at least 99% sequence identity to one or more of the amino acid sequences set forth in SEQ ID NO: 148-SEQ ID NO: 152. A carrier as described herein can comprise at least one of the amino acid sequences set forth in SEQ ID NO: 148-SEQ ID NO: 152. A carrier as described herein can comprise at least two of the amino acid sequences set forth in SEQ ID NO: 148-SEQ ID NO: 152. A carrier as described herein can comprise at least three of the amino acid sequences set forth in SEQ ID NO: 148-SEQ ID NO: 152. A carrier as described herein can comprise at least four of the amino acid sequences set forth in SEQ ID NO: 148-SEQ ID NO: 152. A carrier as described herein can comprise all of the amino acid sequences set forth in SEQ ID NO: 148-SEQ ID NO: 152. Thus, a carrier as described herein can comprise the amino acid sequence set forth in SEQ ID NO: 4 or SEQ ID NO: 5, or a functional fragment thereof.
As disclosed herein, the PE exotoxin domain I (SEQ ID NO: 137) comprises amino acids 1-252 of SEQ ID NO: 135 and has been described as a “receptor binding domain” that functions as a ligand for a cell surface receptor and mediates binding of PE to a cell. Thus, a carrier of the present disclosure can be derived from PE and can comprise the receptor binding domain polypeptide having the amino acid sequence set forth in SEQ ID NO: 137. A carrier can comprise an amino acid sequence with greater than 50% homology to SEQ ID NO: 137. A carrier can comprise an amino acid sequence with greater than 60% homology to SEQ ID NO: 137. A carrier can comprise an amino acid sequence with greater than 70% homology to SEQ ID NO: 137. A carrier can comprise an amino acid sequence with greater than 80% homology to SEQ ID NO: 137. A carrier can comprise an amino acid sequence with greater than 90% homology to SEQ ID NO: 137. A carrier can comprise an amino acid sequence with greater than 95% homology to SEQ ID NO: 137. Moreover, conservative or non-conservative substitutions can be made to the amino acid sequence of SEQ ID NO: 7, so long as the ability to mediate binding of the delivery construct to a cell is not substantially eliminated. A carrier can comprise a receptor binding domain that is a truncated version of SEQ ID NO: 137. A carrier can comprise a receptor binding domain polypeptide wherein one or more amino residues of SEQ ID NO: 137 are deleted. A carrier can comprise a receptor binding domain polypeptide wherein one or more amino residues of SEQ ID NO: 137 are substituted with another amino acid.
A carrier of the present disclosure that is derived from a PE domain I can comprise an amino acid sequence having at least 80% identity to the amino acid sequence of SEQ ID NO: 137 or at least 80% identity to a functional fragment thereof. A carrier can comprise a deletion or mutation in one or more of amino acid residues 1-252 of SEQ ID NO: 137. A carrier can comprise an amino acid sequence having at least 90% sequence identity to the amino acid sequence of 1-252 of SEQ ID NO: 137 or at least 90% sequence identity to a functional fragment thereof. A carrier can comprise an amino acid sequence having at least 95% sequence identity to the amino acid sequence of 1-252 of SEQ ID NO: 137 or at least 95% sequence identity to a functional fragment thereof. A carrier can comprise an amino acid sequence having at least 99% sequence identity to the amino acid sequence of 1-252 of SEQ ID NO: 137 or at least 99% sequence identity to a functional fragment thereof. A carrier can comprise an amino acid sequence having 100% sequence identity to the amino acid sequence of 1-252 of SEQ ID NO: 137 or 100% sequence identity to a functional fragment thereof.
A carrier (e.g., a bacterial carrier receptor binding domain) of the present disclosure can be a polypeptide derived from PE and having: at most 5 amino acid residues; at most 10 amino acid residues; at most 15 amino acid residues; at most 20 amino acid residues; at most 30 amino acid residues; at most 40 amino acid residues; at most 50 amino acid residues; at most 60 amino acid residues; at most 70 amino acid residues; at most 80 amino acid residues; at most 90 amino acid residues; at most 100 amino acid residues; at most 110 amino acid residues; at most 120 amino acid residues; at most 130 amino acid residues; at most 140 amino acid residues; at most 150 amino acid residues; at most 160 amino acid residues; at most 170 amino acid residues; at most 180 amino acid residues; at most 190 amino acid residues; at most 200 amino acid residues; at most 210 amino acid residues; at most 220 amino acid residues; at most 230 amino acid residues; at most 240 amino acid residues; at most 250 amino acid residues; at most 260 amino acid residues; and at most 265 amino acid residues of SEQ ID NO: 137. The bacterial carrier receptor binding domain can be a polypeptide derived from PE and having at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 99%, or more sequence homology with SEQ ID NO: 137. The bacterial carrier receptor binding domain can be a polypeptide derived from PE and having at most 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, or 99% sequence homology with SEQ ID NO: 137. The amino acid residues can be consecutive. The amino acid residues can be non-consecutive.
A carrier of the present disclosure can comprise a binding domain that is an artificially synthesized polypeptide having at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 99%, or more amino acid sequence homology to PE domain I. The carrier comprising a receptor binding domain can be a synthetic polypeptide having at most 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, or 99% amino acid sequence homology to PE domain I set forth in SEQ ID NO: 137. The polypeptide can be synthesized using solid-phase synthesis or recombinant expression.
A carrier of the present disclosure capable of delivering cargo across epithelial cells (e.g., polarized epithelial cells) can comprise a receptor binding domain polypeptide (e.g., a domain I or a derivative thereof) wherein one or more amino acid residues of one bacterial carrier receptor binding domain polypeptide is replaced by one or more amino acid residues of a second bacterial carrier receptor binding domain polypeptide (also referred to hereinafter as “a hybrid receptor binding domain polypeptide”). For example, a carrier can comprise an amino acid sequence wherein one or more amino acid residues of SEQ ID NO: 4 are replaced by one or more amino acid residues of SEQ ID NO: 137. Alternatively, a carrier can comprise an amino acid sequence wherein one or more amino acid residues of SEQ ID NO: 137 are replaced by one or more amino acid residues of SEQ ID NO: 4. Furthermore, such a carrier can comprise an amino acid sequence wherein amino acid residues 77-87 of SEQ ID NO: 4 (Cholix) are replaced by amino acid residues of a second bacterial carrier receptor binding domain polypeptide (e.g., a PE domain I). A carrier can comprise an amino acid sequence wherein amino acid residues 188-236 of SEQ ID NO: 4 are replaced by amino acid residues of a second bacterial carrier receptor binding domain polypeptide. A carrier can comprise an amino acid sequence wherein amino acid residues 69-71 of SEQ ID NO: 137 are replaced by amino acid residues of a second bacterial carrier receptor binding domain polypeptide. A carrier can also comprise an amino acid sequence wherein amino acid residues 177-228 of SEQ ID NO: 137 are replaced by amino acid residues of a second bacterial carrier receptor binding domain polypeptide. Thus, a carrier of the present disclosure can comprise an amino acid sequence having at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 99%, or more sequence homology with SEQ ID NO: 4 and at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 99%, or more sequence homology with SEQ ID NO: 137.
A carrier of the present disclosure that is derived from a domain I of an exotoxin can further comprise a portion of an exotoxin translocation domain, or modified translocation domain elements. A translocation domain can be a domain II of an exotoxin. A carrier of the present disclosure that is derived from a domain I of an exotoxin can further comprise a portion of a non-toxic catalytic domain or modified non-toxic catalytic domain elements. A non-toxic catalytic domain can be a modified domain III of an exotoxin, e.g., those that comprise one or more amino acid variations and/or a deletion of one or more amino acid residues rendering the domain III non-toxic (e.g., an E581A substitution (e.g., SEQ ID NO: 3) or a ΔE581deletion). A translocation domain, or a modified translocation domain, and a non-toxic catalytic domain, or a modified non-toxic catalytic domain, can be derived from the same bacterial toxin. Alternatively, a translocation domain, or a modified translocation domain, and a non-toxic catalytic domain, or a modified non-toxic catalytic domain can be derived from a bacterial carrier selected from the group consisting of Cholix carrier (Cholix) and Pseudomonas exotoxin (PE), botulinum toxin, diptheria toxin, pertussis toxin, cholera toxin, heat-labile E. coli entero-toxin, shiga toxin, and shiga-like toxin.
As described herein, Cholix domain II (SEQ ID NO: 126) comprises amino acids 266-386 of SEQ ID NO: 1). A carrier of the present disclosure can comprise a Cholix derived carrier comprising the entire amino acid sequence of SEQ ID NO: 126, or can comprise a portion(s) of SEQ ID NO: 126. Further, conservative or non-conservative substitutions can be made to SEQ ID NO: 126. A representative assay that can routinely be used by one of skill in the art to determine whether a transcytosis domain has transcytosis activity is described herein. A carrier can comprise at least 1%, at least 5%, at least 10%, at least 20%, at least 30%, at least 40%, at least 50%, at least 60%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, or at least 99% amino acid residues of the entire amino acid sequence of SEQ ID NO: 126. A carrier of the present disclosure can comprise a truncated Cholix domain II, e.g., those identified as Cholix425 (SEQ ID NO: 129), Cholix415 (SEQ ID NO: 130), Cholix397 (SEQ ID NO: 131), Cholix386 (SEQ ID NO: 132), Cholix291(SEQ ID NO: 133), and Cholix265 (SEQ ID NO: 4).
As described herein, a PE domain II (SEQ ID NO: 138) comprises amino acids 253-364 of SEQ ID NO: 135). A carrier of the present disclosure can comprise a PE carrier comprising the entire amino acid sequence of SEQ ID NO: 137, or can comprise a portion(s) of SEQ ID NO: 137. For example, it is demonstrated herein that, similar to the Cholix exotoxin domain I, PE domain I can be sufficient for rapid and efficient apical-to-basal transcytosis. Thus, as described above for Cholix derived carriers, portion(s) of PE domain II can be used as a spacer to attach further payload, such as a heterologous cargo. Further, conservative or non-conservative substitutions can be made to SEQ ID NO: 137. A representative assay that can routinely be used by one of skill in the art to determine whether a transcytosis domain has transcytosis activity is described herein. As used herein, the transcytosis activity is not substantially eliminated so long as the activity is, e.g., at least 1%, at least 5%, at least 10%, at least 20%, at least 30%, at least 40%, at least 50%, at least 60%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95%, or at least 99% as compared to a PE carrier comprising the entire amino acid sequence of SEQ ID NO: 137. Thus, a carrier of the present disclosure can comprise a truncated PE domain II, e.g., those identified as PE404 (SEQ ID NO: 141), PE395 (SEQ ID NO: 142), PE376 (SEQ ID NO: 143), PE364 (SEQ ID NO: 144), PE277 (SEQ ID NO: 145), and PE252 (SEQ ID NO: 137).
A carrier of the present disclosure can comprise a receptor binding domain, and a translocation domain (e.g., a domain II), or a modified translocation domain (e.g., a modified domain II), and can further comprise a non-toxic catalytic domain (e.g., a domain III), or modified non-toxic catalytic domain (e.g., a modified domain III). The non-toxic catalytic domain, or modified non-toxic catalytic domain can be derived from a bacterial carrier selected from the group consisting of Cholix carrier (Cholix) and Pseudomonas exotoxin (PE), botulinum toxin, diptheria toxin, pertussis toxin, cholera toxin, heat-labile E. coli entero-toxin, shiga toxin, and shiga-like toxin. In various embodiments, the translocation domain, or modified translocation domain, and the non-toxic catalytic domain, or modified non-toxic catalytic domain, are derived from the same bacterial toxin.
As described herein, Cholix domain III (SEQ ID NO: 128) comprises amino acids 426-634 of SEQ ID NO: 1 and has been described as a catalytic domain responsible for cytotoxicity and includes an endoplasmic reticulum retention sequence. Domain III mediates ADP ribosylation of elongation factor 2 (“EF2”), which inactivates protein synthesis. A carrier that “lacks endogenous ADP ribosylation activity” or a “detoxified Cholix” refers to any Cholix derived carrier described herein (including modified variants) that does not comprise the entire amino acid sequence set forth in SEQ ID NO: 128 (e.g., a portion of a domain III). Such a carrier can comprise one or more modifications within SEQ ID NO: 128 in a manner which detoxifies the molecule. For example, deletion of the glutamic acid (Glu) residue at amino acid position 156 of SEQ ID NO: 128 detoxifies the molecule. In various embodiments, the portion of SEQ ID NO: 128 other than the ER retention signal can be replaced by another amino acid sequence. This amino acid sequence can itself be non-immunogenic, slightly immunogenic, or highly immunogenic. A highly immunogenic ER retention domain is preferable for use in eliciting a humoral immune response. For example, Cholix domain III is itself highly immunogenic and can be used in delivery constructs where a robust humoral immune response is desired.
As described herein, PE Domain III (SEQ ID NO: 140) comprises amino acids 405-613 of SEQ ID NO: 3) and has been described as a catalytic domain responsible for cytotoxicity and includes an endoplasmic reticulum retention sequence. Domain III mediates ADP ribosylation of elongation factor 2 (“EF2”), which inactivates protein synthesis. A PE derived carrier that “lacks endogenous ADP ribosylation activity” or a “detoxified PE” refers to any PE described herein (including modified variants or derivatives) that does not comprise SEQ ID NO: 140 and/or which has been modified within SEQ ID NO: 140 in a manner which detoxifies the molecule. For example, deletion of the glutamic acid (Glu) residue at amino acid position 149 of SEQ ID NO: 140 detoxifies the molecule. In various embodiments, the portion of PE domain III other than the ER retention signal can be replaced by another amino acid sequence. This amino acid sequence can itself be non-immunogenic, slightly immunogenic, or highly immunogenic. A highly immunogenic ER retention domain is preferable for use in eliciting a humoral immune response. For example, PE domain III is itself highly immunogenic and can be used in delivery constructs where a robust humoral immune response is desired.
The present disclosure contemplates carriers that can comprise a receptor binding domain polypeptide having the amino acid sequence derived from the sequence set forth in SEQ ID NO: 137, a translocation domain having the amino acid sequence derived from the sequence set forth in SEQ ID NO: 138, and a non-toxic catalytic domain having the amino acid sequence derived from the sequence set forth in SEQ ID NO: 140. The present disclosure contemplates carriers that can comprise a receptor binding domain polypeptide having the amino acid sequence derived from the sequence set forth in SEQ ID NO: 4 or SEQ ID NO: 5, a translocation domain having the amino acid sequence derived from the sequence set forth in SEQ ID NO: 126, and a non-toxic catalytic domain having the amino acid sequence derived from the sequence set forth in SEQ ID NO: 128.
In addition to carriers comprising a domain I and/or portions of a domain II and a domain III of an exotoxin, the present disclosure provides carriers that can comprise a Cholix domain Ib (SEQ ID NO: 127), or a portion thereof. Cholix domain Ib (SEQ ID NO: 127) consists of amino acids 387-425 of SEQ ID NO: 1. Thus, a carrier that is derived from a domain I of an exotoxin, can further comprise the amino acid sequence set forth in SEQ ID NO: 127, or a modified sequence truncated at an amino acid residue within SEQ ID NO: 127. The herein described PE domain Ib (SEQ ID NO: 139) consists of amino acids 365-404 of SEQ ID NO: 135. Thus, a PE derived carrier that comprises a receptor binding domain, and a translocation domain, or a modified translocation domain, and a non-toxic catalytic domain, or modified non-toxic catalytic domain, can further comprise the amino acid sequence set forth in SEQ ID NO: 139, or a modified sequence truncated at an amino acid residue within SEQ ID NO: 139.
A carrier of the present disclosure can comprise portion(s) of one or more of a domain II, a domain Ib, or a domain III, wherein those portions (e.g., certain amino acid sequences thereof) can be part of a spacer as further described herein.
The methods and compositions of the present disclosure contemplate carriers that can comprise a first portion and a second portion, wherein the first portion is derived from a first exotoxin and the second portion is derived from a second exotoxin; and wherein the carrier can be coupled to a cargo (e.g., a heterologous cargo such as a biologically active cargo). The first exotoxin can be Cholix, and the second exotoxin can be PE. The first portion can be derived from a domain I, a domain II, a domain Ib, or a domain III of Cholix, or any combination thereof. The first portion can comprise an amino acid sequence having at least 80% sequence identity to any one of the amino acid sequences set forth in SEQ ID NO: 1-SEQ ID NO: 133, a functional fragment thereof, or any combination thereof. The first portion can comprise an amino acid sequence having at least 80% sequence identity to any one of the amino acid sequences set forth in SEQ ID NO: 148-SEQ ID NO: 152, a functional fragment thereof, or any combination thereof. The first portion can comprise an amino acid sequence having at least 80% sequence identity to any one of the amino acid sequences set forth in SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 10, or SEQ ID NO: 11, a functional fragment thereof, or any combination thereof. The second portion can be derived from a domain I, a domain II, a domain Ib, or a domain III of PE, or any combination thereof. The second portion can comprise an amino acid sequence having at least 80% sequence identity to any one of the amino acid sequences set forth in SEQ ID NO: 137-SEQ ID NO: 145, a functional fragment thereof, or any combination thereof. The first portion can be chemically coupled or recombinantly coupled to the second portion. The first portion can further be directly or indirectly coupled to the second portion. Such a carrier can comprise an amino acid sequence having at least 80% sequence identity to the amino acid sequence SEQ ID NO: 146 or SEQ ID NO: 147.
Generally, a carrier of the present disclosure can comprise a polypeptide, wherein the polypeptide can comprise at least 110 amino acid residues of a domain I of the exotoxin. A carrier can comprise at least 120 amino acid residues of a domain I of the exotoxin. A carrier can comprise at least 130 amino acid residues of a domain I of the exotoxin. A carrier can comprise at least 140 amino acid residues of a domain I of the exotoxin. A carrier can comprise at least 150 amino acid residues of a domain I of the exotoxin. A carrier can comprise at least 50 contiguous amino acid residues of the domain I of the exotoxin. A carrier can comprise at least 60 contiguous amino acid residues of the domain I of the exotoxin. A carrier can comprise at least 75 contiguous amino acid residues of the domain I of the exotoxin. A carrier can comprise at least 100 contiguous amino acid residues of the domain I of the exotoxin. A carrier can comprise at least 150 contiguous amino acid residues of the domain I of the exotoxin.
The methods and compositions of the present disclosure contemplate carriers that can comprise on or more modifications at the N-terminal. Such a modification can comprise at least one N-terminal methionine residue. The at least one N-terminal methionine residue can be part of an N-cap as described herein. A carrier comprising an N-cap can further comprise one or more amino acid variations in the first 5-10 amino acid residues compared to a reference sequences. Thus, one or more of the first N-terminal amino acid residues of the amino acid sequence set forth in SEQ ID NO: 1 can be substituted with other amino acid residues, as long as the consensus sequence that can define a functional Cholix is not altered. In addition to such amino acid variations, a carrier described herein comprising an N-cap can further comprise an N-terminal methionine residue. An N-cap can also only comprise an addition of an N-terminal methionine residue. Exemplary carriers of the present disclosure that comprise such N-cap (e.g., an additional N-terminal methionine) are set forth in any one of SEQ ID NO: 5, SEQ ID NO: 7, SEQ ID NO: 9, SEQ ID NO: 11, SEQ ID NO: 31, SEQ ID NO: 107, SEQ ID NO: 125. As described herein, functional variants of such carrier can comprise an amino acid sequence having at least 80% sequence identity to an amino acid sequence set forth in any one of SEQ ID NO: 5, SEQ ID NO: 7, SEQ ID NO: 9, SEQ ID NO: 11, SEQ ID NO: 31, SEQ ID NO: 107, SEQ ID NO: 125, or 80% sequence identity to a functional fragment thereof.
Generally, and as further described herein, a “Cholix” (also referred to herein as Cholix toxin or Cholix exotoxin) can encompass a variety of functional variants (e.g., a functional genus), wherein the functional variants can comprise one or more variations is their amino acid sequence relative to SEQ ID NO: 1 as disclosed herein. Thus, in the present disclosure, the Cholix toxin having the amino acid sequence set forth in SEQ ID NO: 1 is used as the reference sequence when referred to Cholix. However, as described herein, the present disclosure is not limited to the Cholix having the amino acid sequence set forth in SEQ ID NO: 1 but instead encompasses all Cholix variants that fall within the functional genus of Cholix. For example, a first Cholix domain I polypeptide (e.g., a first carrier) can comprise the amino acid sequence set forth in SEQ ID NO: 4, and a second Cholix domain I polypeptide (e.g., a second carrier) can comprise the amino acid sequence set forth in SEQ ID NO: 5, wherein both the first polypeptide and the second polypeptide are capable of carrying out the same functions, e.g., transcytosis across an epithelial cell, and interact with the same receptors, such as ribophilin 1, SEC24, CK-8, TMEM132, GRP75, ERGIC-53, and/or perlecan. As described herein, a first carrier and a second carrier can be produced in the same expression system (e.g., a bacterial expression system such as E. coli or a mammalian expression system such as a CHO cell). In other cases, and as described herein, a first carrier and a second carrier are produced in a different expression system (e.g., a bacterial or a mammalian expression system).
A carrier of the present disclosure can comprise properties that allow interactions with endogenous receptors and/or accessing an endogenous transport and transcytosis system. Thus, a carrier of the present disclosure that is derived from Cholix domain I and comprises an amino acid sequence set forth in any one of SEQ ID NO: 4-SEQ ID NO: 125 or SEQ ID NO: 148-SEQ ID NO: 152 can interact with one or more endogenous receptors. Such endogenous receptors can include TMEM132A, GPR75, ERGIC-53, and/or perlecan, and any combination thereof. Such interaction(s) can provide for (e.g., apical-to-basal) transcytosis across an epithelial cell and/or transport to the interior of an epithelial cell. These interactions allow rapid and efficient delivery. These interactions further provide transport mechanisms that may not alter the carrier of the cell that a carrier is delivered into or transported across. For example, carriers described herein do not show any chemical modifications upon release from the basal membrane of an epithelial cell, suggesting that the carriers of the present disclosure may harness one or more endogenous transport system to deliver cargo into and/or across epithelial cells. Receptors that a carrier and/or a delivery construct comprising a carrier can interact with include, but are not limited to, any one of ribophilin 1, SEC24, CK-8, TMEM132, GRP75, ERGIC-53, or perlecan, or any combination thereof. For example, the interaction of a carrier and/or a delivery construct comprising a carrier with ERGIC-53 (also referred to as LAMN1) can be an integral part of the endocytosis and/or transcytosis process as this receptor is the only interacting protein that may subvert in its cellular distribution following luminal application of a carrier. Moreover, and as demonstrated herein, ERGIC-53 (LAMN1) has been implicated in an indirect retrograde pathway from the Golgi to the ER, suggesting that this can be a pathway described as both efficient and rapid.
The present disclosure provides methods and compositions comprising carriers that allow rapid and efficient transport and delivery of cargo across cells such as epithelial cells. A carrier as described herein can transport cargo across an epithelial cell with a transport rate of about 10−10 cm/sec to about 10−2 cm/sec. A carrier can transport cargo across an epithelial cell with a transport rate of about 10−9 cm/sec to about 10−3 cm/sec. A carrier can transport cargo across an epithelial cell with a transport rate of about 10−8 cm/sec to about 10−4 cm/sec. A carrier can transport cargo across an epithelial cell with a transport rate of about 10−7 cm/sec to about 10−5 cm/sec. A carrier can transport cargo across an epithelial cell with a transport rate of about 10−6 cm/sec. A carrier can transport cargo across an epithelial cell with a transport rate of at least 10−8 cm/sec. A carrier can transport cargo across an epithelial cell with a transport rate of at least 10−7 cm/sec. A carrier can transport cargo across an epithelial cell with a transport rate of at least 10−6 cm/sec. A carrier can transport cargo across an epithelial cell with a transport rate of at least 10−5 cm/sec. A carrier can transport cargo across an epithelial cell with a transport rate of at least 10−4 cm/sec. A carrier can transport cargo across an epithelial cell with a transport rate of at least 10−3 cm/sec. A carrier can transport cargo across an epithelial cell with a transport rate of at least 10−2 cm/sec.
Delivery Constructs
The methods and compositions of the present disclosure provide carrier molecules that rapidly and efficiently transport cargo into and/or across epithelial cells. Delivery and/or transport of cargo can be achieved by coupling the cargo to a carrier as described herein. Such a construct can be referred to herein as a “delivery construct.” As described herein, the present disclosure contemplates carriers that can comprise a small molecule, a polypeptide, an aptamer, a fragment thereof, or any combination thereof. As described herein, a carrier can be derived from an exotoxin. The exotoxin can be Cholix or PE. A carrier can be coupled directly or indirectly to the cargo. A carrier can be covalently or non-covalently coupled to the cargo. Thus, a delivery construct can further comprise a spacer that links the carrier to the cargo. The spacer can be any molecule that links the carrier to the cargo and can comprise oligomeric or polymeric spacers (e.g., polyethylene glycol, etc.), and amino acids. Moreover, a delivery construct comprising a carrier coupled to a cargo and, optionally, a spacer and/or another functional moiety, can be produced synthetically or recombinantly (e.g., in E. coli or a CHO cell).
As disclosed herein, the terms “delivery constructs”, “delivery constructs”, “toxin-derived delivery constructs”, “chimeric constructs”, “proteins” and “fusion proteins” can be used interchangeably and can refer to constructs comprising at least one delivery or carrier domain (e.g., a Cholix or PE domain I derived carrier, a small molecule, an aptamer, or any combination thereof) and at least one heterologous cargo molecule such as a therapeutic cargo molecule. The term “heterologous cargo” can be referred to as unrelated to these exotoxins. As further described herein, toxicity (e.g., intoxication of enterocytes) of the bacterial carrier (e.g., Cholix or PE) may not be a necessary requirement for efficient transport of the carrier across intact epithelial layers such as the gut epithelium. Instead, it is demonstrated herein that a carrier that is derived from a domain I (e.g., a truncated version of a domain I) of an exotoxin such as Cholix and PE is sufficient for rapid and efficient transcytosis across epithelial cell (e.g., polarized epithelial cells of a gut).
Generally, a delivery construct (e.g., an isolated delivery construct) comprises a carrier that provides rapid and efficient delivery and/or transport of a cargo to a certain location, wherein the location can be an organ, a tissue, a cell, or a cellular compartment. The cargo molecule can be directly or indirectly coupled to the carrier. The cargo that is coupled to the carrier can be a heterologous cargo (e.g., not derived from the carrier itself). Thus, a delivery construct described herein can comprise a carrier coupled to a heterologous cargo. The carrier can comprise certain functions that allow repaid and efficient transport of cargo to a location, e.g., a location within an epithelial cell or a location(s) within a basolateral compartment. A carrier contemplated herein can be derived from an exotoxin. The exotoxin can be Cholix or PE. A carrier that is derived from a Cholix can comprise an amino acid sequence having at least 80% sequence identity to SEQ ID NO: 1, or at least 80% sequence identity to a functional fragment thereof. It is noted that a Cholix (also referred to herein as Cholix toxin or Cholix exotoxin) can encompass a variety of functional variants (e.g., a functional genus), wherein the functional variants can comprise one or more variations is their amino acid sequence relative to SEQ ID NO: 1 as disclosed herein. Thus, in the present disclosure, the Cholix toxin having the amino acid sequence set forth in SEQ ID NO: 1 is used as the reference sequence when referred to Cholix. However, as described herein, the present disclosure is not limited to the Cholix having the amino acid sequence set forth in SEQ ID NO: 1 but instead encompasses all Cholix variants that fall within the functional genus of Cholix. For example, a first Cholix domain I polypeptide (e.g., a first carrier) can comprise the amino acid sequence set forth in SEQ ID NO: 4, and a second Cholix domain I polypeptide (e.g., a second carrier) can comprise the amino acid sequence set forth in SEQ ID NO: 5, wherein both the first polypeptide and the second polypeptide are capable of carrying out the same functions, e.g., transcytosis across an epithelial cell, and interact with the same receptors, such as ribophilin 1, SEC24 (can also be referred to as COPII coat complex component), cytokeratin-8 (CK-8), transmembrane protein 132 (TMEM132), glucose regulated protein 75 (GRP75), endoplasmatic reticulum Golgi intermediate compartment 53 (ERGIC-53, the number 53 may refer to its molecular weight of approximately 53 kDa), and/or perlecan (also referred to as basement membrane-specific heparan sulfate proteoglycan core protein or HSPG). As described herein, a first carrier and a second carrier can be produced in the same expression system (e.g., a bacterial expression system such as E. coli or a mammalian expression system such as a CHO cell). As described herein, a first carrier and a second carrier can be produced in a different expression system (e.g., a bacterial or a mammalian expression system).
Importantly, the delivery constructs contemplated herein can provide advantages over conventional delivery modalities. Such advantages can include, but are not limited to: a) aid in the production of the delivery construct; b) aid in the refolding of the chimera construct; c) aid in the formulation of the delivery construct; d) aid in reducing the sensitivity of the cargo to proteolytic destruction; e) improve the stability of the delivery construct during storage; f) in embodiments wherein the bacterial carrier elements of domain I are coupled to the heterologous (e.g., a biologically active) cargo without a spacer, or with a non-cleavable spacer, the bacterial carrier elements of domain I can function to retain the chimera to selected locations in the body following transcytosis that results in greater exposure of a biologically active (or diagnostic) cargo to specific cells to provide improved pharmacodynamics; g) in embodiments wherein the bacterial carrier elements of domain I are coupled to a heterologous (e.g., biologically active) cargo with a spacer that is cleavable by an enzyme present at a basolateral membrane of an epithelial cell, or an enzyme present in the plasma of the subject, such cleavage will allow the heterologous (e.g., biologically active) cargo to be released from the remainder of the construct soon after transcytosis across the epithelial membrane; h) the direct delivery of the heterologous cargo to the interior of an epithelial cell such as an intracellular vesicle or compartment or the cytosol or a supranuclear region of an epithelial cell; i) the direct delivery of the heterologous (e.g., biologically active) cargo to the submucosal-GI space and hepatic-portal system can reduce the systemic toxicity observed when the cargo is administered by parenteral routes, as well as enabling access to the submucosal target biology that would be difficult to target via non-oral or GI routes; j) by using endogenous transport and delivery mechanisms, the delivery constructs disclosed herein do not damage the epithelial layer; k) once transported across the GI epithelium, the delivery construct or the biologically active cargo will exhibit an extended serum half-life compared to the biologically active cargo in its non-fused state; 1) oral administration of the delivery construct can deliver an increased effective concentration of the delivered biologically active cargo to the liver of the subject than is observed in the subject's plasma; and m) the ability to deliver the biologically active cargo to a subject without using a needle to puncture the skin of the subject, thus improving such subjects' quality of life by avoiding pain or potential complications associated therewith, in addition to improved patient/care-giver convenience and compliance.
The present disclosure provides methods and compositions for delivery and transport of cargo molecules across an epithelial cell (e.g., via transcytosis) and/or into the interior of an epithelial cell. The methods and compositions disclosed herein can comprise a delivery construct, wherein the delivery construct comprises a carrier coupled to a heterologous cargo (e.g., via a spacer). The transport and delivery processes described herein using the carriers of the present disclosure can comprise endocytosis on the apical side of an epithelial cell. Depending on whether the carrier is configured to deliver cargo into or across an epithelial cell, the transport processes can comprise the release of the delivery construct on the basal side. Furthermore, various mechanisms can be involved in transporting cargo to those various locations. For example, delivery of cargo to an intracellular vesicle or compartment or the cytosol of an epithelial cell can comprise releasing a delivery construct comprising a carrier coupled to that cargo from a vesicle into the an intracellular vesicle or compartment or the cytosol. As another example, transcytosis of a delivery construct can include vesicular transcytosis and, as such, can comprise encapsulating the delivery construct in a vesicle during transcytosis such that the delivery construct may or may not be in contact with the intracellular cytosol.
The methods and compositions of the present disclosure can comprise delivering a cargo to a certain location such that the cargo remains at that location for a certain amount of time. For example, a cargo molecule can be retained at an intracellular or basolateral location that has been targeted using the compositions described herein. Retention can cause the cargo molecule to elicit a certain response or biological effect (e.g., a therapeutic effect). Thus, the present disclosure provides methods and compositions that allow delivery of cargo to a location within across an epithelial cell such the delivery construct (and the cargo) is retained at that location for a specific amount of time. Such retention can be modulated, e.g., by allowing the cargo to be cleaved from the carrier, or by allowing the carrier to reversibly or irreversibly bind a certain protein (e.g., a receptor) that is present at that location.
The delivery constructs of the present disclosure can comprise a carrier, wherein the carrier can be configured to target a certain location inside or across an epithelial cell. Such a location can be an organ, a tissue, a cell, or a cellular compartment. By targeting such locations, the methods and compositions described herein can be used for various applications, e.g., those that include delivery of cargo across an intact epithelial membrane in vitro or in vivo.
As described herein, a carrier can be coupled to a heterologous cargo in any way described herein. A delivery construct comprises a carrier that is coupled to a heterologous cargo via a spacer. The spacer can comprise any moiety recited herein, and can comprise any one of the amino acid sequences set forth in SEQ ID NO: 166-SEQ ID NO: 213. The spacer can be a cleavable spacer. The spacer can be a non-cleavable spacer. A spacer can comprise the amino acid sequence set forth in SEQ ID NO: 210, or a fragment or derivative thereof.
Generally, and as described herein, any carrier disclosed herein (e.g., those listed in TABLE 2 and TABLE 3) can be combined with any one of the cargo molecules described herein (e.g., those listed in TABLE 11 and TABLE 12), and, optionally, with any spacer described herein (e.g., those listed in TABLES 7-10 and those having an amino acid sequence set forth in SEQ ID NO: 207-SEQ ID NO: 213) to form a delivery construct. Thus, a carrier described herein can be derived from an exotoxin. A carrier can be derived from a domain I of an exotoxin. The exotoxin can be Cholix or PE. A delivery construct contemplated herein can comprise a carrier derived from Cholix, wherein the carrier can comprise an amino acid sequence having at least 80% sequence identity to an amino acid sequence set forth in any one of SEQ ID NO: 1-SEQ ID NO: 125, coupled to a heterologous cargo. A carrier can comprise an amino acid sequence having at least 90% sequence identity to an amino acid sequence set forth in any one of SEQ ID NO: 1-SEQ ID NO: 125. A carrier can comprise an amino acid sequence having at least 95% sequence identity to an amino acid sequence set forth in any one of SEQ ID NO: 1-SEQ ID NO: 125. A carrier can comprise an amino acid sequence having at least 99% sequence identity to an amino acid sequence set forth in any one of SEQ ID NO: 1-SEQ ID NO: 125. The exotoxin that a carrier can be derived from can be PE. Thus, a delivery construct comprises a carrier can comprise an amino acid sequence having at least 80% sequence identity to an amino acid sequence set forth in SEQ ID NO: 137, or a functional fragment thereof, coupled to a heterologous cargo.
Exemplary delivery constructs as described in the present disclosure are shown below in TABLE 4.
The methods and compositions of the present disclosure can comprise a delivery construct comprising an amino acid sequence having at least 80% sequence identity to an amino acid sequence set forth in any one of SEQ ID NO: 153-SEQ ID NO: 165, or having at least 80% sequence identity to a functional fragment thereof. A delivery construct can comprise an amino acid sequence having at least 90% sequence identity to an amino acid sequence set forth in any one of SEQ ID NO: 153-SEQ ID NO: 165, or having at least 90% sequence identity to a functional fragment thereof. A delivery construct can comprise an amino acid sequence having at least 95% sequence identity to an amino acid sequence set forth in any one of SEQ ID NO: 153-SEQ ID NO: 165, or having at least 95% sequence identity to a functional fragment thereof. A delivery construct can comprise an amino acid sequence having at least 99% sequence identity to an amino acid sequence set forth in any one of SEQ ID NO: 153-SEQ ID NO: 165, or having at least 99% sequence identity to a functional fragment thereof. A delivery construct can comprise an amino acid sequence having 100% sequence identity to an amino acid sequence set forth in any one of SEQ ID NO: 153-SEQ ID NO: 165, or having 100% sequence identity to a functional fragment thereof.
Exemplary combinations of various carriers, spacers, and heterologous cargos that can form a delivery construct as described herein are shown below in TABLE 5.
A delivery construct of the present disclosure can interact with one or more specific proteins, enzyme, or receptors during transport and/or delivery across an epithelial cell and/or into the interior of an epithelial cell (e.g., a polarized gut epithelial cell). The one or more receptors can be endogenous receptors. Thus, the delivery constructs of the present disclosure can use endogenous receptor systems that provide for rapid efficient transport and delivery of cargo across an epithelial cell or an intact epithelium (e.g., a monolayer of Caco-2 cells and/or an intact gut epithelium of a subject), and/or to the interior of an epithelial cell of an epithelium. Delivery constructs comprising a carrier comprising an amino acid sequence set forth in any one of SEQ ID NO: 30-SEQ ID NO: 125 can enable delivery and transport of a heterologous (e.g., a therapeutically or biologically active) cargo to the interior of an epithelial cell, e.g., to the basal side of an epithelial cell, and/or a supranuclear region (e.g., the endoplasmatic reticulum, the Golgi apparatus, and/or an endosome) of an epithelial cell. The interior of an epithelial cell can be an intracellular vesicle or compartment or the cytosol of the epithelial cell. A cargo (e.g., a heterologous cargo) can be delivered to the basal side of the epithelial cell (e.g., a location or compartment at the basal side). A heterologous cargo can be delivered to a supranuclear region of the epithelial cell. Transport of a delivery construct to the interior of an epithelial cell can comprise releasing the delivery construct from a vesicle that formed during endocytosis of the delivery construct on the apical surface of the epithelial cell. Delivery and/or transport to a location in the interior of a cell can comprise retaining the delivery construct in a vesicle and/or releasing the delivery construct from that vesicle, such that the delivery construct can be in contact with the cytosol of the epithelial cell (e.g., the construct may or may not be in contact with the cytosol of the epithelial cell during transcytosis due to encapsulation in the vesicle). Thus, a carrier comprising a truncated version of Cholix domain I can be released from a vesicle, e.g., those comprising an amino acid sequence set forth in any one of SEQ ID NO: 30-SEQ ID NO: 107, or a functional fragment or derivative thereof.
Delivery constructs of the present disclosure comprising a carrier comprising an amino acid sequence set forth in any one of SEQ ID NO: 4-SEQ ID NO: 29, SEQ ID NO: 129-SEQ ID NO: 133, or SEQ ID NO: 141-SEQ ID NO: 145 can enable delivery and transport of a heterologous (e.g., a therapeutically or biologically active) cargo across an epithelial cell. Transport across an epithelial cell (e.g., a polarized gut epithelial cell) can occur via transcytosis. The transcytosis mechanism utilized by the herein described delivery constructs is an endogenous trafficking system including a variety of distinct receptors that the delivery construct interacts with. A carrier of a delivery construct can comprise the structural elements that allow these receptor interactions. The receptors that a carrier as disclosed herein can interact with include ribophilin 1, SEC24, CK-8, TMEM132, GRP75, ERGIC-53, and perlecan, or any combination thereof. A carrier as described herein may not or may not significantly interact with clathrin or GPR78, or a combination thereof.
Using an endogenous system including those receptors can have several advantages over other transport mechanisms. Using an endogenous transport system can include the following advantages: (i) an intact layer of epithelial cells such as a monolayer or an epithelium in vivo can be crossed without damaging or disrupting the cells or monolayer structure; (ii) rapid and efficient delivery and transport can be achieved; (iii) the interaction of distinct domains or regions of an exotoxin derived construct with specific receptors allows modulation of these interaction in a way that allows to specifically target certain regions or compartments within a cell or within a subject. For example, delivery and transport (e.g., of a heterologous cargo) to the interior of an epithelial cell can be provided by using certain truncated versions of an exotoxin domain I, such as those having an amino acid sequence set forth in any one of SEQ ID NO: 30-SEQ ID NO: 125, or functional fragment thereof. The epithelial cell can be located in the gut of a subject (e.g., a rodent or a human). In various embodiments, delivery and transport (e.g., of a heterologous cargo) across an epithelial layer via transcytosis (e.g., by using an endogenous transcytosis system) can be provided by using certain truncated versions or derivatives of an exotoxin domain I, such as those having an amino acid sequence set forth in any one SEQ ID NO: 4-SEQ ID NO: 29, SEQ ID NO: 129-SEQ ID NO: 133, or SEQ ID NO: 141-SEQ ID NO: 145. The ability of the herein described delivery constructs to rapidly and efficiently deliver therapeutically active and/or diagnostic cargo to those locations enables new options for treatment, prevention, and/or diagnosis of various diseases (e.g., inflammatory disease, autoimmune diseases, hormone-deficiency diseases, obesity and metabolic disorders, and cancer).
Delivery constructs of the present disclosure, in addition to a carrier, a cargo, and, optionally, a spacer, can further comprise one or more functional moieties. A functional moiety can be a detectable agent, an affinity handle (e.g., a clickable functional groups such as an azide), a barcode (e.g., a nucleic acid barcode), cell-penetrating agents, or other functional moieties that modulate the pharmacokinetic (PK) and/or pharmacodynamic (PD) profile of the delivery construct. A delivery construct can comprise a cell-penetrating agent. The cell-penetrating agent can be a peptide. The cell-penetrating agent can comprise polycations, polyorganic acids, endosomal releasing polymers, poly(2-propylacrylic acid), poly(2-ethylacrylic acid), Tat peptide, Arg patch, a knotted peptide, CysTAT, S19-TAT, R8 (SEQ ID NO: 73), pAntp, Pas-TAT, Pas-R8 (SEQ ID NO: 76), Pas-FHV, Pas-pAntP, F2R4 (SEQ ID NO: 79), B55, aurin, IMT-P8, BR2, OMOTAG1, OMOTAG2, pVEC, SynB3, DPV1047, C105Y, Transpotan, MTS, hLF, PFVYLI (SEQ ID NO: 93), maurocalcine, imperatoxin, hadrucalin, hemicalcin, opicalcin-1, opicalcin-2, midkin(62-104), MCoTI-II, or a chlorotoxin. A cell-penetrating agent can be coupled to a delivery construct as described herein via the N- or the C-terminus. A cell-penetrating agent can provide access to a variety of cell types. A cell-penetrating agent can provide additional functionality, e.g., for therapeutic cargo delivery, once the delivery construct has crossed and epithelial layer (e.g., an epithelium of a subject).
The methods and compositions of the present disclosure contemplate delivery constructs that can form a multimer. A multimer comprising multiple delivery constructs can be formed in solution. A multimer can be formed by multimerization of the carrier and/or the heterologous cargo. The multimer can be a heteromer or a homomer. The homomer can be a homodimer. The homodimer can be formed by dimerization of the heterologous cargo. For example, a delivery construct comprising the amino acid sequence set forth in SEQ ID NO: 217 can form a dimer. Dimerization of such a delivery construct can be due to dimerization of the cargo, e.g., IL-10 (e.g., SEQ ID NO: 217) in this case.
Insertion Site for Attachment of the Heterologous Cargo
The methods and compositions of the present disclosure can comprise a delivery construct comprising a carrier coupled to a cargo, such as a heterologous cargo. A heterologous (e.g., biologically active) cargo re can be attached to the carrier (e.g., a small molecule, a polypeptide, an aptamer, or a nucleic acid) by any method known by one of skill in the art without limitation. The heterologous cargo can be introduced into any portion of the carrier that does not disrupt the endocytosis and/or transcytosis activity of the carrier.
The present disclosure provides delivery constructs that comprise a polypeptide carrier. Thus, a heterologous cargo can be directly coupled to the N-terminus or C-terminus of such a polypeptide carrier (e.g., a domain I or a truncated version thereof, e.g., SEQ ID NO: 4-SEQ ID NO: 125). A heterologous cargo can be couple to the carrier via a side chain of an amino acid of the carrier receptor binding domain. A heterologous cargo can be coupled to the carrier with a cleavable spacer such that cleavage at the cleavable spacer(s) separates the heterologous cargo from the remainder of the delivery construct. A heterologous cargo can be also a polypeptide that comprises a short leader peptide that remains attached to the polypeptide following cleavage of the cleavable spacer. For example, the heterologous cargo can comprise a short leader peptide of greater than 1 amino acid, greater than 5 amino acids, greater than 10 amino acids, greater than 15 amino acids, greater than 20 amino acids, greater than 25 amino acids, greater than 30 amino acids, greater than 50 amino acids, or greater than 100 amino acids. A biological active cargo can comprise a short leader peptide of less than 100 amino acids, less than 50 amino acids, less than 30 amino acids, less than 25 amino acids, less than 20 amino acids, less than 15 amino acids, less than 10 amino acids, or less than 5 amino acids. A biological active cargo can comprise a short leader peptide of between 1-100 amino acids, between 5-10 amino acids, between 10 to 50 amino acids, or between 20 to 80 amino acids.
As described herein, the present disclosure provides methods and compositions comprising carrier that are derived from a domain I of an exotoxin, wherein the exotoxin can be Cholix or PE. In native Cholix (e.g., SEQ ID NO: 1 or SEQ ID NO: 2) and PE (e.g., SEQ ID NO: 135) the domain Ib loop is not essential for any known activity of the toxin, including cell binding, translocation, ER retention or ADP ribosylation activity. Accordingly, domain Ib can be deleted entirely, or modified to contain a heterologous cargo, e.g., a biologically active cargo. Thus, the heterologous cargo (e.g., biologically active cargo) can be inserted into Cholix or PE carrier domain Ib. A heterologous cargo (e.g., biologically active cargo), for example, can be inserted into a Cholix derived carrier domain Ib between the cysteines at positions 395 and 402 that are not cross-linked. This can be accomplished by reducing the disulfide linkage between the cysteines, by deleting one or both of the cysteines entirely from the Ib domain, by mutating one or both of the cysteines to other residues, for example, serine, or by other similar techniques. Alternatively, the biologically active cargo can be inserted into the domain Ib loop between the cysteines at positions 395 and 402. In such embodiments, the disulfide linkage between the cysteines can be used to constrain the biologically active cargo domain.
The methods and compositions described herein can comprise delivery constructs that are produced such that a heterologous cargo is expressed together with a carrier (and, optionally, a spacer) as a fusion protein (e.g., the delivery construct). In such cases, the heterologous cargo can be inserted into the delivery construct by any method known to one of skill in the art without limitation. For example, amino acids corresponding to the heterologous cargo can be directly inserted into the receptor binding domain, with or without deletion of native amino acid sequences. Alternatively, a heterologous cargo may not be expressed together with a carrier (and, optionally, a spacer) as a fusion protein, the heterologous cargo can be coupled to the carrier by any suitable method known by one of skill in the art, without limitation, including peptide conjugation chemistry and/or click chemistry.
Spacers
The methods and compositions of the present disclosure can comprise delivery constructs comprising a carrier coupled to a cargo (e.g., a heterologous cargo), wherein the carrier is capable of delivering the heterologous cargo into and/or across an epithelial cell in vitro (e.g., an epithelial cell monolayer) or in vivo (e.g., a gut epithelium of a subject). Such a carrier can be coupled to a cargo in any way described herein. The carrier can be directly or indirectly coupled the cargo. The carrier can also be covalently or non-covalently coupled to the cargo.
The present disclosure provides delivery constructs comprising a carrier coupled to a heterologous cargo via a spacer. A spacer can comprise any moiety recited herein. A spacer can be any molecule that links the carrier to the cargo and can comprise oligomeric or polymeric spacers (e.g., polyethylene glycol, etc.), other small molecule spacer (e.g., those derived from dicarbonic acids such as succinic acid, aspartic acid, etc.) and amino acids (including short peptide sequences etc.). Thus, a “spacer,” as described herein, generally refers to a chemical moiety that can be attached to or coupled to a molecule of the present disclosure. A spacer can be located between a first molecule and a second molecule. A spacer can connect, attach, link, or couple a first molecule (e.g., a polypeptide, small molecule, nucleic acid, etc.) to a second molecule (e.g., a polypeptide, small molecule, nucleic acid, etc.). A spacer can reduce steric hindrance between the first molecule and the second molecule. A spacer can be an amino acid sequence coupled to the C-terminus of a peptide or polypeptide. The amino acid sequence of a spacer as disclosed herein can be between 1-100 amino acid residues long. A spacer can be between 5-75 amino acid residues long. A spacer can be between 5-50 amino acid residues long. In some cases, a spacer is between 5-25 amino acid residues long. A carrier can comprise any one of the amino acid sequences set forth in SEQ ID NO: 4-SEQ ID NO: 125 is coupled to a spacer at its C-terminus (and the spacer can be further coupled to a heterologous cargo via its C-terminus). The spacer can be an amino acid spacer. The spacer can comprise any of the amino acid sequences set forth in SEQ ID NO: 166-SEQ ID NO: 213. The spacer can comprise a portion of a domain II, a domain Ib, or a domain III of an exotoxin, or any combination thereof. For example, a delivery construct as described herein can comprise a carrier comprising an amino acid sequence set forth in any one of SEQ ID NO: 4-SEQ ID NO: 125, coupled to a spacer, wherein the spacer comprises amino acid residues 1-82 of SEQ ID NO: 126.
The present disclosure provides delivery constructs that comprise one or more spacer which are further described herein. A spacer can comprise an amino acid sequence. A spacer can comprise at most 82 amino acid residues of any one SEQ ID NO: 126. Thus, a spacer can comprise the first 82 amino acid residues of the amino acid sequence set forth in SEQ ID NO: 126. The amino acid residues of the Cholix domain II can be contiguous amino acid residues (e.g., residues 1-82 of SEQ ID NO: 126).
Other spacer that can be used in combination with the herein described methods and compositions comprise those comprising an amino acid sequences set forth in SEQ ID NO: 207-SEQ ID NO: 211. A spacer comprises the amino acid sequence set forth in SEQ ID NO: 210, or a fragment or derivative thereof.
The methods and compositions of the present disclosure can comprise spacer that can comprise a portion of a domain II, a domain Ib, and/or a domain III of an exotoxin. For example, a carrier comprising an amino acid sequence set forth in any one of SEQ ID NO: 4-SEQ ID NO: 125 can further be coupled (e.g., via the C-terminus) to a spacer, wherein the spacer comprises from about 80 to about 90 amino acid residues from any one of SEQ ID NO: 126-SEQ ID NO: 128 and/or SEQ ID NO: 138-SEQ ID NO: 140. A spacer can comprise at most 85 amino acid residues of any one of SEQ ID NO: 126-SEQ ID NO: 128 and/or SEQ ID NO: 137-SEQ ID NO: 139. A spacer can comprise at most 82 amino acid residues of any one of SEQ ID NO: 126-SEQ ID NO: 128 and/or SEQ ID NO: 137-SEQ ID NO: 139 A spacer can comprise at most 80 amino acid residues of any one of SEQ ID NO: 126-SEQ ID NO: 128 and/or SEQ ID NO: 137-SEQ ID NO: 139. A spacer can comprise at most 50 amino acid residues of any one of SEQ ID NO: 126-SEQ ID NO: 128 and/or SEQ ID NO: 137-SEQ ID NO: 139. A spacer can comprise at most 25 amino acid residues of any one of SEQ ID NO: 126-SEQ ID NO: 128 and/or SEQ ID NO: 137-SEQ ID NO: 139.
A spacer can comprise at most 82 amino acid residues of any one SEQ ID NO: 126. A spacer can comprise the first 82 amino acid residues of the amino acid sequence set forth in SEQ ID NO: 126. The amino acid residues of the Cholix domain II can be contiguous amino acid residues (e.g., residues 1-82 of SEQ ID NO: 126).
A spacer of the present disclosure can be a cleavable spacer. A spacer of the present disclosure can be a non-cleavable spacer.
Cleavable Spacers
The presently described methods and compositions allow for a heterologous cargo (e.g., a biologically or therapeutically active cargo) to be delivered to a location inside or across an epithelial cell, wherein the heterologous cargo can be coupled to the carrier forming a delivery construct as described herein. Such a delivery construct can further comprise a spacer that can indirectly couple a carrier to a cargo (e.g., a heterologous cargo). A spacer as described herein can be a cleavable spacer. The number of cleavable spacers present in a delivery construct depends, at least in part, on the location of the heterologous cargo in relation to the delivery construct and the nature of the heterologous cargo. When the heterologous cargo can be separated from the remainder of the delivery construct with cleavage at a single spacer, the delivery constructs can comprise a single cleavable spacer. Further, where the heterologous cargo is, e.g., a dimer or other multimer, each subunit of the biologically active cargo can be separated from the remainder of the delivery construct and/or the other subunits of the biologically active cargo by cleavage at the cleavable spacer.
A cleavable spacer can be cleaved by a cleaving enzyme that is present at or near the basolateral membrane of an epithelial cell. By selecting the cleavable spacer to be cleaved by such enzymes, the biologically active cargo can be liberated from the remainder of the delivery construct following transcytosis across the mucous membrane and release from the epithelial cell into the cellular matrix on the basolateral side of the membrane. Further, cleaving enzymes could be used that are present inside the epithelial cell, such that the cleavable spacer is cleaved prior to release of the delivery construct from the basolateral membrane, so long as the cleaving enzyme does not cleave the delivery construct before the delivery construct enters the trafficking pathway in the polarized epithelial cell that results in release of the delivery construct and biologically active cargo from the basolateral membrane of the cell.
A carrier of the present disclosure can be cleaved by an enzyme. The enzyme that is present at a basolateral membrane of a polarized epithelial cell can be selected from, e.g., Cathepsin GI, Chymotrypsin I, Elastase I, Subtilisin AI, Subtilisin AII, Thrombin I, or Urokinase I. TABLE 6 presents these enzymes together with an amino acid sequence that is recognized and cleaved by the particular peptidase.
A cleavable spacer can exhibit a greater propensity for cleavage than the remainder of the delivery construct. As one skilled in the art is aware, many peptide and polypeptide sequences can be cleaved by peptidases and proteases. The cleavable spacer can be selected so that it will be preferentially cleaved relative to other amino acid sequences present in the delivery construct during administration of the delivery construct. A carrier of a delivery construct can be substantially (e.g., about 99%, about 95%, about 90%, about 85%, about 80, or about 75%) intact following delivery of the delivery construct to the bloodstream of the subject. A cargo of a delivery construct can be substantially (e.g., about 99%, about 95%, about 90%, about 85%, about 80, or about 75%) intact following delivery of the delivery construct to the bloodstream of the subject. A cleavable spacer can be substantially (e.g., about 99%, about 95%, about 90%, about 85%, about 80, or about 75%) cleaved following delivery of the delivery construct to the bloodstream of the subject.
A cleaving enzyme found in the plasma of the subject can be used to cleave the cleavable spacer. Any cleaving enzyme known by one of skill in the art to be present in the plasma of the subject can be used to cleave the cleavable spacer. Uses of such enzymes to cleave the cleavable spacers is less preferred than use of cleaving enzymes found near the basolateral membrane of a polarized epithelial cell because it is believed that more efficient cleavage will occur in near the basolateral membrane. However, if the skilled artisan determines that cleavage mediated by a plasma enzyme is sufficiently efficient to allow cleavage of a sufficient fraction of the delivery constructs to avoid adverse effects; such plasma cleaving enzymes can be used to cleave the delivery constructs. Accordingly, the cleavable spacer can be cleaved with an enzyme that is selected from the group consisting of caspase-1, caspase-3, proprotein convertase 1, proprotein convertase 2, proprotein convertase 4, proprotein convertase 4 PACE 4, prolyl oligopeptidase, endothelin cleaving enzyme, dipeptidyl-peptidase IV, signal peptidase, neprilysin, renin, and esterase (see, e.g., U.S. Pat. No. 6,673,574, incorporated by reference in its entirety herein). TABLE 7 presents these enzymes together with an amino acid sequence(s) recognized by the particular peptidase. The peptidase cleaves a peptide comprising these sequences at the N-terminal side of the amino acid identified with an asterisk.
Thus, a cleavable spacer can be any cleavable spacer known by one of skill in the art to be cleavable by an enzyme that is present at the basolateral membrane of an epithelial cell. A cleavable spacer can comprise a peptide. A cleavable spacer can comprise a nucleic acid, such as RNA or DNA. Furthermore, a cleavable spacer can comprise a carbohydrate, such as a disaccharide or a trisaccharide.
Alternatively, a cleavable spacer can be any cleavable spacer known by one of skill in the art to be cleavable by an enzyme that is present in the plasma of the subject to whom the delivery construct is administered. Such a cleavable spacer can comprise a peptide. Such a cleavable spacer can comprise a nucleic acid, such as RNA or DNA. Such a cleavable spacer comprises a carbohydrate, such as a disaccharide or a trisaccharide.
A cleavable spacer can be selected from, or can be derived from the exemplary list presented in TABLE 8.
Moreover, a cleavable spacer can be a spacer that comprises an amino acid sequence that is a known substrate for the tobacco etch virus (TEV) protease. Accordingly, a cleavable spacer can comprise the amino acid sequence set in forth in, e.g., GGGGSGGGENLYFQS (SEQ ID NO: 193).
The novel delivery constructs of the present disclosure can comprise a peptide sequence (or like domain), which serves to inhibit, interfere with, or block the ability of the biologically active cargo to bind to receptors at the surface of epithelial cells. Accordingly, depending upon the biologically cargo to be delivered, the peptide sequence (or like domain) which serves to inhibit, interfere with, or block the ability of the biologically active cargo to bind to its receptor at the surface of epithelial cells will be directed specifically to the receptor to which the biologically active binds.
Various biologically active cargos can bind to GM-1-gangliosides found on the surfaces of mammalian cells. Accordingly, a cleavable spacer of the present disclosure can comprise a peptide sequence, which serves to inhibit, interfere with, or block the ability of the biologically active cargo to bind GM-1 at the surface of epithelial cells. U.S. Pat. No. 8,877,161 teach a number of peptides that interfere with the binding of ligands to GM-1. TABLE 9 presents several examples of peptide sequences, which can be incorporated in whole, or in part, into the cleavable spacers to be used in the preparation of the delivery constructs of the present disclosure.
A cleavable spacer used in the preparation of the delivery constructs of the present disclosure can comprise the amino acid sequence of, e.g., SEQ ID NO: 185, SEQ ID NO: 186, SEQ ID NO: 187, SEQ ID NO: 188, SEQ ID NO: 189 and SEQ ID NO: 190, or variants or fragments thereof, as depicted in TABLE 10 below.
Non-Cleavable Spacers
A delivery construct of the present disclosure can comprise a carrier coupled to a heterologous cargo (e.g., a biologically active cargo), wherein the cargo can be separated from the carrier by a spacer consisting of one or more amino acids (e.g., up to 25 amino acids). The spacer can be a peptide spacer or any other molecular entity that may be used to couple to link a first and a second molecule. Generally, a spacer will have no specific biological activity other than to join the proteins or to preserve some minimum distance or other spatial relationship between them. However, the constituent amino acids of the spacer can be selected to influence some property of the molecule such as the folding, net charge, or hydrophobicity.
The spacer can be capable of forming covalent bonds to both the delivery construct and to the (e.g., biologically active) cargo. Suitable spacers are well known to those of skill in the art and include, but are not limited to, straight or branched-chain carbon spacers, heterocyclic carbon spacers, or peptide spacers. The spacer(s) can be joined to the constituent amino acids of the delivery construct and/or the biologically active cargo through their side groups (e.g., through a disulfide linkage to cysteine). The spacers can be joined to the alpha carbon amino and/or carboxyl groups of the terminal amino acids of the delivery construct and/or the (e.g., biologically active) cargo.
A bifunctional spacer having one functional group capable of reacting with a group on the bacterial carrier and another group reactive on the biologically active cargo can be used to form the desired conjugate. Alternatively, derivatization can involve chemical treatment of the targeting moiety. Procedures for generation of, for example, free sulfhydryl groups on polypeptides, such as antibodies or antibody fragments, are known (See U.S. Pat. No. 4,659,839).
Many procedures and spacer molecules for attachment of various compounds including radionuclide metal chelates, toxins and drugs to proteins such as antibodies are known. See, for example, European Patent Application No. 188,256; U.S. Pat. Nos. 4,671,958, 4,659,839, 4,414,148, 4,699,784; 4,680,338; 4,569,789; and 4,589,071; and Borlinghaus et al. (1987) Cancer Res. 47: 4071-4075.
A cargo (e.g., a biologically active cargo) to be delivered to a location (e.g., a location within a subject such as a human) can be coupled to the carrier using one or more non-cleavable peptide spacers comprising, e.g., the amino acid sequence GTGGS (SEQ ID NO: 207), GGGGS (SEQ ID NO: 208), GGGGSGGGGS (SEQ ID NO: 209), GGGGSGGGGSGGGGS (SEQ ID NO: 210), or GGGGSGGG (SEQ ID NO: 211), wherein the carrier targets said cargo (e.g., biologically active cargo) to specific cells, including but not limited to, cells of the immune system such as macrophages, antigen-presenting cells and dendritic cells (e.g., upon transporting the cargo across an epithelial cell). Generally, a non-cleavable spacer can comprise one or more of (GGGGS)x (SEQ ID NO: 212), wherein x=1, 2, 3, 4, 5, 6, 7, 8, 9, or 10. A non-cleavable spacer can comprise one or more of (GS)x (SEQ ID NO: 213), wherein x=1, 2, 3, 4, 5, 6, 7, 8, 9, or 10.
Production of Delivery Constructs
The delivery constructs of the present disclosure can be produced using a variety of methods. The selection of a production method can depend on the molecular structure of the delivery construct and/or its components (e.g., the carrier, cargo, and/or spacer). Thus, for some delivery constructs organic synthetic methods may be advantageous for producing such delivery construct. A delivery construct of the present disclosure can be a polypeptide. Such polypeptides can be produced, for example, using recombinant DNA methodology. Generally, this involves creating a DNA sequence that encodes the delivery construct, placing the DNA in an expression cassette under the control of a particular promoter, expressing the molecule in a host, isolating the expressed molecule and, if required, folding of the molecule into an active conformational form.
DNA encoding the delivery constructs described herein can be prepared by any suitable method, including, for example, cloning and restriction of appropriate sequences or direct chemical synthesis by methods such as the phosphotriester method of Narang et al. (1979) Meth. Enzymol. 68: 90-99; the phosphodiester method of Brown et al. (1979) Meth. Enzymol. 68: 109-151; the diethylphosphoramidite method of Beaucage et al. (1981) Tetra. Lett., 22: 1859-1862); the solid support method of U.S. Pat. No. 4,458,066, and the like.
Chemical synthesis produces a single stranded oligonucleotide. This can be converted into double stranded DNA by hybridization with a complementary sequence or by polymerization with a DNA polymerase using the single strand as a template. One of skill would recognize that while chemical synthesis of DNA is limited to sequences of about 100 bases, longer sequences can be obtained by the ligation of shorter sequences.
Alternatively, subsequences can be cloned and the appropriate subsequences cleaved using appropriate restriction enzymes. The fragments can then be ligated to produce the desired DNA sequence. A DNA encoding a delivery constructs of the present disclosure can be cloned using DNA amplification methods such as polymerase chain reaction (PCR). Thus, for example, the gene for the biologically active cargo is PCR amplified, using a sense primer containing the restriction site for, e.g., NdeI and an antisense primer containing the restriction site for HindIII. This can produce a nucleic acid encoding the biologically active cargo sequence and having terminal restriction sites. A delivery construct having “complementary” restriction sites can similarly be cloned and then ligated to the biologically active cargo and/or to a spacer attached to the biologically active cargo. Ligation of the nucleic acid sequences and insertion into a vector produces a vector encoding the biologically active cargo joined to the bacterial carrier receptor binding domain. In various embodiments, DNA encoding delivery constructs of the present disclosure is artificially synthesized by, for example, solid-phase DNA synthesis.
The production methods described herein can be used to produce the delivery constructs of the present disclosure, or (functional) variants thereof. For example, a “Cholix” (also referred to herein as Cholix toxin or Cholix exotoxin) can encompass a variety of functional variants (e.g., a functional genus), wherein the functional variants can comprise one or more variations is their amino acid sequence relative to SEQ ID NO: 1 as disclosed herein. Thus, in the present disclosure, the Cholix toxin having the amino acid sequence set forth in SEQ ID NO: 1 is used as the reference sequence when referred to Cholix. However, as described herein, the present disclosure is not limited to the Cholix having the amino acid sequence set forth in SEQ ID NO: 1 but instead encompasses all Cholix variants that fall within the functional genus of Cholix. For example, a variant of the Cholix exotoxin with the amino acid sequence set forth in SEQ ID NI: 1 can be a Cholix exotoxin which amino acid sequence is set forth in SEQ ID NO: 2, wherein both variants are capable of carrying out the same functions, e.g., transcytosis across an epithelial cell, and interact with the same receptors, such as ribophilin 1, SEC24, CK-8, TMEM132, GRP75, ERGIC-53, and/or perlecan.
Moreover, the production method of a polypeptide can affect, to some degree, the amino acid sequence of such polypeptide (e.g., due to post-translational modifications). For example, a first carrier and a second carrier are produced in the same expression system (e.g., a bacterial expression system such as E. coli or a mammalian expression system such as a CHO cell). In other cases, and as described herein, a first carrier and a second carrier are produced in a different expression system (e.g., a bacterial or a mammalian expression system). Bacterial expression systems include E. coli, and mammalian expression systems include CHO cells, for example. A bacterially produced polypeptide can comprise an N-cap, wherein the N-cap can comprise one more modifications at the N-terminal of the polypeptide. An N-cap can comprise an N-terminal methionine residue. Examples of Cholix domain I derived carrier polypeptides that can be bacterially produced and that comprise such N-terminal methionine include those comprising the amino acid sequences set forth in SEQ ID NO: 5, SEQ ID NO: 7, SEQ ID NO: 9, SEQ ID NO: 11, SEQ ID NO: 31, SEQ ID NO: 107, and SEQ ID NO: 135.
Cargo
The present disclosure provides methods and compositions that allow for the rapid and efficient delivery of cargo into and/or across epithelial cells (e.g., polarized epithelial cells) in vitro (e.g., a Caco-2 cell monolayer) and in vivo (e.g., a gut epithelium of a subject). Such rapid and efficient delivery can be achieved by coupling the cargo (e.g., a biologically active cargo) to a carrier to form a delivery construct. Such delivery constructs can be modified to target certain locations within an epithelial cell or to transport cargo across an epithelial cell such as an intact epithelial membrane.
In various embodiments, the compositions and methods of the present disclosure provide efficient transport and delivery of various cargo molecules to different locations (e.g., organs, tissues, or cells) of a subject (e.g., a rodent or a human). The delivery constructs of the present disclosure can allow for delivery into epithelial cells and/or for rapid transcytosis (e.g., vesicular transcytosis) across an epithelial cell layer such as a gut epithelium of a subject. The presently described delivery mechanisms allow for transport and delivery of various cargo molecules. The herein described delivery constructs can be coupled to at least one, at least two, at least three, at least five or at least 10 cargo molecules. The cargo can be a heterologous cargo, e.g., heterologous to the carrier. For example, a delivery construct described herein comprises a Cholix domain I derived carrier (e.g., those having the amino acid sequences set forth in SEQ ID NO: 1-SEQ ID NO: 125) coupled to a heterologous cargo, wherein the heterologous cargo is a non-Cholix derived cargo molecule (e.g., is not derived or does not contain fragments of a Cholix toxin domain I, II, Ib, and III).
A heterologous cargo can be a biologically active cargo. A biologically active cargo can include therapeutic and/or diagnostic molecules. Thus, the delivery constructs of the present disclosure can be used to deliver a biologically active cargo to a subject (e.g., a rodent or a human). A “biologically active cargo” as used herein includes, but is not limited to: a macromolecule, small molecule, peptide, polypeptide, nucleic acid, mRNA, miRNA, shRNA, siRNA, antisense molecule, antibody, DNA, plasmid, vaccine, polymer nanoparticle, or catalytically-active material.
A biologically active cargo of the present disclosure can be a macromolecule that can perform a desirable biological activity when introduced to the bloodstream of the subject. For example, the biologically active cargo can have receptor binding activity, enzymatic activity, messenger activity (i.e., act as a hormone, cytokine, neurotransmitter, or other signaling molecule), luminescent or other detectable activity, or regulatory activity, or any combination thereof. For certain diagnostic purposes, a biologically active cargo can be conjugated to or can itself be a pharmaceutically acceptable gamma-emitting moiety, including but not limited to, indium and technetium, magnetic particles, radiopaque materials such as air or barium and fluorescent compounds.
A heterologous cargo as described herein can be a biologically active cargo. A biologically active cargo that is part of a delivery construct can exert its effects in biological compartments of the subject other than the subject's blood. For example, in various embodiments, the biologically active cargo can exert its effects in the lymphatic system. In other cases, the biologically active cargo can exert its effects in an organ or tissue, such as, for example, the subject's liver, heart, lungs, pancreas, kidney, brain, bone marrow, etc. As such, the biologically active cargo can or cannot be present in the blood, lymph, or other biological fluid at detectable concentrations, yet can still accumulate at sufficient concentrations at its site of action to exert a biological effect.
A biologically active cargo can be a protein that comprises more than one polypeptide subunit. For example, the protein can be a dimer, trimer, or higher order multimer. In various embodiments, two or more subunits of the protein can be connected with a covalent bond, such as, for example, a disulfide bond. The subunits of the protein can be held together with non-covalent interactions. One of skill in the art can routinely identify such proteins and determine whether the subunits are properly associated using, for example, an immunoassay.
A biologically active cargo to be delivered to a certain location (e.g., in a subject) can be selected from, e.g., cytokines and cytokine receptors such as Interleukin-1 (IL-1), IL-2, IL-3, IL-4, IL-5, IL-6, IL-7, IL-8, IL-9, IL-10, IL-11, IL-12, IL-13, IL-14, IL-15, IL-16, IL-17, IL-18, IL-19, IL-20, IL-21, IL-22, IL-23, IL-24, IL-25, IL-26, IL-27, IL-28, IL-29, IL-30, lymphokine inhibitory factor, macrophage colony stimulating factor, platelet derived growth factor, stem cell factor, tumor growth factor-β, tumor necrosis factor, lymphotoxin, Fas, granulocyte colony stimulating factor, granulocyte macrophage colony stimulating factor, interferon-α, interferon-β, interferon-γ, growth factors and protein hormones such as erythropoietin, angiogenin, hepatocyte growth factor, fibroblast growth factor, keratinocyte growth factor, nerve growth factor, tumor growth factor-a, thrombopoietin, thyroid stimulating factor, thyroid releasing hormone, neurotrophin, epidermal growth factor, VEGF, ciliary neurotrophic factor, LDL, somatomedin, insulin growth factor, insulin-like growth factor I and II, chemokines such as ENA-78, ELC, GRO-α, GRO-β, GRO-γ, HRG, LEF, IP-10, MCP-1, MCP-2, MCP-3, MCP-4, MIP-1-α, MIP-1-β, MG, MDC, NT-3, NT-4, SCF, LIF, leptin, RANTES, lymphotactin, eotaxin-1, eotaxin-2, TARC, TECK, WAP-1, WAP-2, GCP-1, GCP-2; α-chemokine receptors, e.g., CXCR1, CXCR2, CXCR3, CXCR4, CXCR5, CXCR6, CXCR7; and β-chemokine receptors, e.g., CCR1, CCR2, CCR3, CCR4, CCR5, CCR6, CCR7.
An illustrative, but not limiting, list of suitable biologically active cargo to be used in the constructs and methods of the present invention is provided in TABLE 11.
A biologically active cargo as described herein can be a hormone. Such a hormone can be a growth hormone. The hormone can be a human growth hormone having, for example, the amino acid sequence set forth in SEQ ID NO: 214.
A biologically active cargo can be a molecule affects and/or interacts with a metabolism of a subject. Thus, a biologically active cargo as described herein can be a drug that can be used to prevent, treat and/or diagnose a metabolic disease or condition. Thus, a biologically active cargo as described herein can be a glucagon-like peptide (GLP). The GLP can be GLP-1 having the amino acid sequence set forth in SEQ ID NO: 215. A hormone that can be used in combination with the methods and compositions described herein can be insulin (with c-peptide element removed from mature protein), or a derivative thereof. An Insulin peptide can comprise the amino acid sequence set forth in SEQ ID NO: 216.
A biologically active cargo can be an interleukin. Specifically, interleukins that can be used with the methods and compositions described herein can include IL-10 and IL-22, having the amino acid sequence set forth in SEQ ID NO: 217 and SEQ ID NO: 218, respectively.
The biologically active cargo disclosed herein can modulate the spatial orientation of a delivery construct. For example, a cargo molecule can induce multimerization of two or more delivery constructs. Such multimers can be homomers or heteromers. The multimer can be a homodimer. For example, a delivery construct comprising the amino acid sequence set forth in SEQ ID NO: 217 can form a dimer. Such dimerization can be induced by IL-10 (as IL-10 can form a natural dimer and thus promote dimerization of a delivery construct comprising an IL-10 as cargo).
A biologically active cargo can also comprise toxin, such as endotoxins, enterotoxins or exotoxins. For example, a biologically active cargo can be an ExtB polypeptide (which will form a natural pentamer) having the amino acid sequence set forth in SEQ ID NO: 219.
Other examples of biologically active cargo that can be delivered according to the present disclosure include, but are not limited to, antineoplastic compounds, such as nitrosoureas, e.g., carmustine, lomustine, semustine, strepzotocin; methylhydrazines, e.g., procarbazine, dacarbazine; steroid hormones, e.g., glucocorticoids, estrogens, progestins, androgens, tetrahydrodesoxycaricosterone; immunoactive compounds such as immunosuppressives, e.g., pyrimethamine, trimethopterin, penicillamine, cyclosporine, azathioprine; and immunostimulants, e.g., levamisole, diethyl dithiocarbamate, enkephalins, endorphins; antimicrobial compounds such as antibiotics, e.g., β-lactam, penicillin, cephalosporins, carbapenims and monobactams, β-lactamase inhibitors, aminoglycosides, macrolides, tetracyclins, spectinomycin; antimalarials, amebicides; antiprotazoals; antifungals, e.g., amphotericin β, antivirals, e.g., acyclovir, idoxuridine, ribavirin, trifluridine, vidarbine, gancyclovir; parasiticides; antihalmintics; radiopharmaceutics; gastrointestinal drugs; hematologic compounds; immunoglobulins; blood clotting proteins, e.g., antihemophilic factor, factor IX complex; anticoagulants, e.g., dicumarol, heparin Na; fibrolysin inhibitors, e.g., tranexamic acid; cardiovascular drugs; peripheral anti-adrenergic drugs; centrally acting antihypertensive drugs, e.g., methyldopa, methyldopa HCl; antihypertensive direct vasodilators, e.g., diazoxide, hydralazine HCl; drugs affecting renin-angiotensin system; peripheral vasodilators, e.g., phentolamine; anti-anginal drugs; cardiac glycosides; inodilators, e.g., amrinone, milrinone, enoximone, fenoximone, imazodan, sulmazole; antidysrhythmics; calcium entry blockers; drugs affecting blood lipids, e.g., ranitidine, bosentan, rezulin; respiratory drugs; sypathomimetic drugs, e.g., albuterol, bitolterol mesylate, dobutamine HCl, dopamine HCl, ephedrine So, epinephrine, fenfluramine HCl, isoproterenol HCl, methoxamine HCl, norepinephrine bitartrate, phenylephrine HCl, ritodrine HCl; cholinomimetic drugs, e.g., acetylcholine Cl; anticholinesterases, e.g., edrophonium Cl; cholinesterase reactivators; adrenergic blocking drugs, e.g., acebutolol HCl, atenolol, esmolol HCl, labetalol HCl, metoprolol, nadolol, phentolamine mesylate, propanolol HCl; antimuscarinic drugs, e.g., anisotropine methylbromide, atropine SO4, clinidium Br, glycopyrrolate, ipratropium Br, scopolamine HBr; neuromuscular blocking drugs; depolarizing drugs, e.g., atracurium besylate, hexafluorenium Br, metocurine iodide, succinylcholine Cl, tubocurarine Cl, vecuronium Br; centrally acting muscle relaxants, e.g., baclofen; neurotransmitters and neurotransmitter agents, e.g., acetylcholine, adenosine, adenosine triphosphate; amino acid neurotransmitters, e.g., excitatory amino acids, GABA, glycine; biogenic amine neurotransmitters, e.g., dopamine, epinephrine, histamine, norepinephrine, octopamine, serotonin, tyramine; neuropeptides, nitric oxide, K+ channel toxins; antiparkinson drugs, e.g., amaltidine HCl, benztropine mesylate, carbidopa; diuretic drugs, e.g., dichlorphenamide, methazolamide, bendroflumethiazide, polythiazide; antimigraine drugs, e.g, carboprost tromethamine mesylate, methysergide maleate.
Still other examples of biologically active cargo that can be delivered according to the present disclosure include, but are not limited to, hormones such as pituitary hormones, e.g., chorionic gonadotropin, cosyntropin, menotropins, somatotropin, iorticotropin, protirelin, thyrotropin, vasopressin, lypressin; adrenal hormones, e.g., beclomethasone dipropionate, betamethasone, dexamethasone, triamcinolone; pancreatic hormones, e.g., glucagon, insulin; parathyroid hormone, e.g., dihydrochysterol; thyroid hormones, e.g., calcitonin etidronate disodium, levothyroxine Na, liothyronine Na, liotrix, thyroglobulin, teriparatide acetate; antithyroid drugs; estrogenic hormones; progestins and antagonists; hormonal contraceptives; testicular hormones; gastrointestinal hormones, e.g., cholecystokinin, enteroglycan, galanin, gastric inhibitory polypeptide, epidermal growth factor-urogastrone, gastric inhibitory polypeptide, gastrin-releasing peptide, gastrins, pentagastrin, tetragastrin, motilin, peptide YY, secretin, vasoactive intestinal peptide, or sincalide.
Still other examples of biologically active cargo that can be delivered according to the present disclosure include, but are not limited to, enzymes such as hyaluronidase, streptokinase, tissue plasminogen activator, urokinase, PGE-adenosine deaminase; intravenous anesthetics such as droperidol, etomidate, fetanyl citrate/droperidol, hexobarbital, ketamine HCl, methohexital Na, thiamylal Na, thiopental Na; antiepileptics, e.g., carbamazepine, clonazepam, divalproex Na, ethosuximide, mephenyloin, paramethadione, phenyloin, primidone. In various embodiments, the biologically active cargo is an enzyme selected from hyaluronidase, streptokinase, tissue plasminogen activator, urokinase, PGE-adenosine deaminase.
A biologically active cargo as described herein can also include a therapeutic and/or diagnostic antibody, an antibody fragment, a diabody, a minibody, or a single-chain variable fragment (e.g., scFv), or a combination thereof. For example, a biologically active cargo as described herein can be an anti-tumor necrosis factor alpha (anti-TNFa) agent. An anti-TNFa agent is an anti-TNFa antibody or a functional fragment thereof. An Anti-TNFa antibody can be adalimumab (Abbvie HUMIRA®, Drug Bank DB 00051) or infliximab (Centocor REMICADE®, Drug Bank DB 00065), or functional fragment (e.g., a binding fragment thereof).
Yet other examples of biologically active cargo that can be delivered according to the present disclosure include, but are not limited to, chemotherapeutics, such as chemotherapy or anti-tumor agents which are effective against various types of human cancers, including leukemia, lymphomas, carcinomas, sarcomas, myelomas etc., such as, for example, doxorubicin, mitomycin, cisplatin, daunorubicin, bleomycin, actinomycin D, and neocarzinostatin.
Yet other examples of biologically active cargo that can be delivered according to the present disclosure include inhibitors of regulatory T cells (Tregs) such as Tregs that express CD4, CD25 and Foxp3, and Tregs such as Tr1, Th3, CD8+CD28−, Qa-1 restricted T cells, and IL-17 Treg cells. Such Treg inhibitors have been extensively studied and described in the art (see, e.g., Casares et al, Journal of Immunology, 185(9): 5150-5159, 2010, and references cited therein).
TABLE 12 shows exemplary amino acid sequences of various heterologous cargos that can be used in combination with the herein disclosed methods and compositions. For example, any of the heterologous cargo molecules shown in TABLE 12 below can be combined with any carrier disclosed herein, e.g., those carrier listed in TABLE 2 and/or TABLE 3 above.
A cargo molecule of the present disclosure can comprise an amino acid sequence having at least 80% sequence identity to any one of the amino acid sequences set forth in SEQ ID NO: 214-SEQ ID NO: 220, at least 80% sequence identity to a functional fragment thereof, and/or any combination of thereof. A cargo molecule of the present disclosure can comprise an amino acid sequence having at least 90% sequence identity to any one of the amino acid sequences set forth in SEQ ID NO: 214-SEQ ID NO: 220, at least 80% sequence identity to a functional fragment thereof, and/or any combination of thereof. A cargo molecule of the present disclosure can comprise an amino acid sequence having at least 95% sequence identity to any one of the amino acid sequences set forth in SEQ ID NO: 214-SEQ ID NO: 220, at least 80% sequence identity to a functional fragment thereof, and/or any combination of thereof. A cargo molecule of the present disclosure can comprise an amino acid sequence having at least 99% sequence identity to any one of the amino acid sequences set forth in SEQ ID NO: 214-SEQ ID NO: 220, at least 80% sequence identity to a functional fragment thereof, and/or any combination of thereof. A cargo molecule of the present disclosure can comprise any one of the amino acid sequences set forth in SEQ ID NO: 214-SEQ ID NO: 220, a functional fragment thereof, and/or any combination of thereof.
Generally, a cargo described and disclosed herein can be retained at a location that has been targeted using the compositions described herein. Retention can cause the cargo molecule to elicit a certain response or biological effect (e.g., a therapeutic effect). The delivery of a molecule (e.g., a heterologous cargo) to a location (e.g., an intracellular compartment or a supranuclear region) can refer to the retention of the molecule at that location. Retention of a molecule at a certain intracellular or extracellular region or compartment can be for a certain amount of time, e.g., at least 2 minutes, at least 5 minutes, at least 10 minutes, at least 15 minutes, at 30 minutes, or at least 60 minutes. Retention of a molecule can depend on various factors such as the location where the molecule is retained and/or the types of molecular interactions that occur between the molecule (e.g., a carrier, a delivery construct, and/or a heterologous cargo). For example, delivery of a heterologous cargo to a basolateral compartment via transcytosis across a polarized epithelial cell can comprise retaining the heterologous cargo at the basolateral location for a time sufficient to elicit a certain effect, such as a therapeutic effect in case of a therapeutic and/or biologically active cargo. A delivery construct can be configured to release a cargo at a specific location, e.g., by using pH-dependent and/or enzyme-dependent spacer. Upon release of a cargo from a carrier, the cargo molecule can elicit a certain effect and/or response. For example, and in the case of biologically and/or therapeutically active cargos, such cargos can elicit their therapeutic effects in vitro or in vivo upon release from the carrier. A cargo may also be capable of eliciting a response when still bound to the carrier. This may depend on the cargo and/or the delivery construct.
A heterologous cargo can be a detectable agent such as a fluorescent molecule or a radioactive moiety. A detectable agent as described herein can be used to detect the molecule that the detectable agent is coupled to in various locations, e.g., inside a subject or inside a cell. A detectable agent can also have additional features and functions, such as therapeutic or other biological properties. For example, a radionuclide coupled to a carrier as described herein can allow the detection of the carrier but can also have therapeutic properties, e.g., as a therapeutic radionuclide. Generally, a carrier can conjugated to, linked to, or fused with detectable agents, such as a fluorophore, a near-infrared dye, a contrast agent, a nanoparticle, a metal-containing nanoparticle, a metal chelate, an X-ray contrast agent, a PET agent, a metal, a radioisotope, a dye, radionuclide chelator, or another suitable material that may be used in imaging.
A delivery construct can comprise about 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 detectable agents. Non-limiting examples of radioisotopes that may be used as detectable agents include alpha emitters, beta emitters, positron emitters, and gamma emitters. The metal or radioisotope may be selected from the group consisting of actinium, americium, bismuth, cadmium, cesium, cobalt, europium, gadolinium, iridium, lead, lutetium, manganese, palladium, polonium, radium, ruthenium, samarium, strontium, technetium, thallium, and yttrium. The metal may be actinium, bismuth, lead, radium, strontium, samarium, or yttrium. The radioisotope may be actinium-225 or lead-212. The near-infrared dyes that may be used in combination with the herein described chimeric binding agents may not be easily quenched by biological tissues and fluids. The fluorophore may be a fluorescent agent emitting electromagnetic radiation at a wavelength between 650 nm and 4000 nm, such emissions being used to detect such agent. Non-limiting examples of fluorescent dyes that may be used as a conjugating molecule in the present disclosure include DyLight-680, DyLight-750, VivoTag-750, DyLight-800, IRDye-800, VivoTag-680, Cy5.5, or indocyanine green (ICG). Near infrared dyes may include cyanine dyes (e.g., Cy7, Cy5.5, and Cy5). Additional non-limiting examples of fluorescent dyes for use as a conjugating molecule in the present disclosure may include acradine orange or yellow, Alexa Fluors (e.g., Alexa Fluor 790, 750, 700, 680, 660, and 647) and any derivative thereof, 7-actinomycin D, 8-anilinonaphthalene-1-sulfonic acid, ATTO dye and any derivative thereof, auramine-rhodamine stain and any derivative thereof, bensantrhone, bimane, 9-10-bis(phenylethynyl)anthracene, 5,12-bis(phenylethynyl)naththacene, bisbenzimide, brainbow, calcein, carbodyfluorescein and any derivative thereof, 1-chloro-9,10-bis(phenylethynyl)anthracene and any derivative thereof, DAPI, DiOC6, DyLight Fluors and any derivative thereof, epicocconone, ethidium bromide, FlAsH-EDT2, Fluo dye and any derivative thereof, FluoProbe and any derivative thereof, Fluorescein and any derivative thereof, Fura and any derivative thereof, GelGreen and any derivative thereof, GelRed and any derivative thereof, fluorescent proteins and any derivative thereof, m isoform proteins and any derivative thereof such as mCherry, hetamethine dye and any derivative thereof, hoeschst stain, iminocoumarin, indian yellow, indo-1 and any derivative thereof, laurdan, lucifer yellow and any derivative thereof, luciferin and any derivative thereof, luciferase and any derivative thereof, mercocyanine and any derivative thereof, nile dyes and any derivative thereof, perylene, phloxine, phyco dye and any derivative thereof, propium iodide, pyranine, rhodamine and any derivative thereof, ribogreen, RoGFP, rubrene, stilbene and any derivative thereof, sulforhodamine and any derivative thereof, SYBR and any derivative thereof, synapto-pHluorin, tetraphenyl butadiene, tetrasodium tris, Texas Red, Titan Yellow, TSQ, umbelliferone, violanthrone, yellow fluorescent protein and YOYO-1. Other Suitable fluorescent dyes may include, but are not limited to, fluorescein and fluorescein dyes (e.g., fluorescein isothiocyanine or FITC, naphthofluorescein, 4′, 5′-dichloro-2′,7′-dimethoxyfluorescein, 6-carboxyfluorescein or FAM, etc.), carbocyanine, merocyanine, styryl dyes, oxonol dyes, phycoerythrin, erythrosin, eosin, rhodamine dyes (e.g., carboxytetramethyl-rhodamine or TAMRA, carboxyrhodamine 6G, carboxy-X-rhodamine (ROX), lissamine rhodamine B, rhodamine 6G, rhodamine Green, rhodamine Red, tetramethylrhodamine (TMR), etc.), coumarin and coumarin dyes (e.g., methoxycoumarin, dialkylaminocoumarin, hydroxycoumarin, aminomethylcoumarin (AMCA), etc.), Oregon Green Dyes (e.g., Oregon Green 488, Oregon Green 500, Oregon Green 514, etc.), Texas Red, Texas Red-X, SPECTRUM RED, SPECTRUM GREEN, cyanine dyes (e.g., CY-3, Cy-5, CY-3.5, CY-5.5, etc.), ALEXA FLUOR dyes (e.g., ALEXA FLUOR 350, ALEXA FLUOR 488, ALEXA FLUOR 532, ALEXA FLUOR 546, ALEXA FLUOR 568, ALEXA FLUOR 594, ALEXA FLUOR 633, ALEXA FLUOR 660, ALEXA FLUOR 680, etc.), BODIPY dyes (e.g., BODIPY FL, BODIPY R6G, BODIPY TMR, BODIPY TR, BODIPY 530/550, BODIPY 558/568, BODIPY 564/570, BODIPY 576/589, BODIPY 581/591, BODIPY 630/650, BODIPY 650/665, etc.), IRDyes (e.g., IRD40, IRD 700, IRD 800, etc.), and the like. Additional suitable detectable agents are described in PCT/US14/56177. Non-limiting examples of radioisotopes include alpha emitters, beta emitters, positron emitters, and gamma emitters. The metal or radioisotope may be selected from the group consisting of actinium, americium, bismuth, cadmium, cesium, cobalt, europium, gadolinium, iridium, lead, lutetium, manganese, palladium, polonium, radium, ruthenium, samarium, strontium, technetium, thallium, and yttrium. The metal may be actinium, bismuth, lead, radium, strontium, samarium, or yttrium. The radioisotope may be actinium-225 or lead-212. Additionally, the following radionuclides may be used for diagnosis and/or therapy: carbon (e.g., 11C or 14C), nitrogen (e.g., 13N), fluorine (e.g., 18F), gallium (e.g., 67Ga or 68Ga), copper (e.g., 64Cu or 67Cu), zirconium (e.g., 89Zr), lutetium (e.g., 177Lu).
A delivery construct as disclosed herein can be conjugated to, coupled to, or fused to a radiosensitizer or photosensitizer. Examples of radiosensitizers may include but are not limited to: ABT-263, ABT-199, WEHI-539, paclitaxel, carboplatin, cisplatin, oxaliplatin, gemcitabine, etanidazole, misonidazole, tirapazamine, and nucleic acid base derivatives (e.g., halogenated purines or pyrimidines, such as 5-fluorodeoxyuridine). Examples of photosensitizers may include but are not limited to: fluorescent molecules or beads that generate heat when illuminated, nanoparticles, porphyrins and porphyrin derivatives (e.g., chlorins, bacteriochlorins, isobacteriochlorins, phthalocyanines, and naphthalocyanines), metalloporphyrins, metallophthalocyanines, angelicins, chalcogenapyrrillium dyes, chlorophylls, coumarins, flavins and related compounds such as alloxazine and riboflavin, fullerenes, pheophorbides, pyropheophorbides, cyanines (e.g., merocyanine 540), pheophytins, sapphyrins, texaphyrins, purpurins, porphycenes, phenothiaziniums, methylene blue derivatives, naphthalimides, nile blue derivatives, quinones, perylenequinones (e.g., hypericins, hypocrellins, and cercosporins), psoralens, quinones, retinoids, rhodamines, thiophenes, verdins, xanthene dyes (e.g., eosins, erythrosins, rose bengals), dimeric and oligomeric forms of porphyrins, and prodrugs such as 5-aminolevulinic acid. Advantageously, this approach may allow for highly specific targeting of diseased cells (e.g., cancer cells) using both a therapeutic agent (e.g., drug) and electromagnetic energy (e.g., radiation or light) concurrently. The proteins of the present disclosure can be conjugated to, coupled to, fused with, or covalently or non-covalently coupled to the agent, e.g., directly or via a spacer.
A radionuclide may be attached to a carrier or delivery construct as described herein using a chelator. Exemplary chelator moieties may include 2,2′,2″-(3-(4-(3-(1-(4-(1,2,4,5-tetrazin-3-yl)phenyl)-1-oxo-5,8,11,14,17,20,23-heptaoxa-2-azapentacosan-25-yl)thioureido)benzyl)-1,4,7-triazonane-2,5,8-triyl)triacetic acid; 2,2′,2″-(3-(4-(3-(1-(4-(1,2,4,5-tetrazin-3-yl)phenyl)-1-oxo-5,8,11,14,17,20,23,26,29,32,35-undecaoxa-2-azaheptatriacontan-37-yl)thioureido)benzyl)-1,4,7-triazonane-2,5,8-triyl)triacetic acid; 2,2′-(7-(4-(3-(1-(4-(1,2,4,5-tetrazin-3-yl)phenyl)-1-oxo-5,8,11,14,17,20,23,26,29,32,35-undecaoxa-2-azaheptatriacontan-37-yl)thioureido)benzyl)-1,4,7-triazonane-1,4-diyl)diacetic acid; 2,2′,2″-(3-(4-(3-(1-(4-(1,2,4,5-tetrazin-3-yl)phenyl)-3,7-dioxo-11,14,17,20,23,26,29-heptaoxa-2,8-diazahentriacontan-31-yl)thioureido)benzyl)-1,4,7-triazonane-2,5,8-triyl)triacetic acid; 2,2′,2″-(3-(4-(3-(1-(4-(1,2,4,5-tetrazin-3-yl)phenyl)-3,7-dioxo-11,14,17,20,23,26,29,32,35,38,41-undecaoxa-2,8-diazatritetracontan-43-yl)thioureido)benzyl)-1,4,7-triazonane-2,5,8-triyl)triacetic acid; 2,2′,2″-(3-(4-(3-(25,28-dioxo-28-((6-(6-(pyridin-2-yl)-1,2,4,5-tetrazin-3-yl)pyridin-3-yl)amino)-3,6,9,12,15,18,21-heptaoxa-24-azaoctacosyl)thioureido)benzyl)-1,4,7-triazonane-2,5,8-triyl)triacetic acid; 2,2′,2″-(3-(4-(3-(37,40-dioxo-40-((6-(6-(pyridin-2-yl)-1,2,4,5-tetrazin-3-yl)pyridin-3-yl)amino)-3,6,9,12,15,18,21,24,27,30,33-undecaoxa-36-azatetracontyl)thioureido)benzyl)-1,4,7-triazonane-2,5,8-triyl)triacetic acid; 2,2′,2″-(3-(4-(1-(4-(6-methyl-1,2,4,5-tetrazin-3-yl)phenyl)-3-oxo-6,9,12,15,18,21,24-heptaoxa-2-azaheptacosan-27-amido)benzyl)-1,4,7-triazonane-2,5,8-triyl)triacetic acid; 2,2′,2″-(2-(4-(1-(4-(6-methyl-1,2,4,5-tetrazin-3-yl)phenoxy)-3,6,9,12,15,18,21,24,27,30,33-undecaoxahexatriacontan-36-amido)benzyl)-1,4,7-triazonane-1,4,7-triyl)triacetic acid; 2,2′,2″-(3-(4-(3-(5-amino-6-((4-(6-methyl-1,2,4,5-tetrazin-3-yl)benzyl)amino)-6-oxohexyl)thioureido)benzyl)-1,4,7-triazonane-2,5,8-triyl)triacetic acid; 2,2′-(7-(4-(3-(5-amino-6-((4-6-methyl-1,2,4,5-tetrazin-3-yl)benzyl)amino)-6-oxohexyl)thioureido)benzyl)-1,4,7-triazonane-1,4-diyl)diacetic acid; 2,2′,2″-(3-(4-(3-(5-amino-6-((5-amino-6-((4-(6-methyl-1,2,4,5-tetrazin-3-yl)benzyl)amino)-6-oxohexyl)amino)-6-oxohexyl)thioureido)benzyl)-1,4,7-triazonane-2,5,8-triyl)triacetic acid; and 2,2′,2″-(3-(4-(3-(5-amino-6-((5-amino-6-((5-amino-6-((4-(6-methyl-1,2,4,5-tetrazin-3-yl)benzyl)amino)-6-oxohexyl)amino)-6-oxohexyl)amino)-6-oxohexyl)thioureido)benzyl)-1,4,7-triazonane-2,5,8-triyl)triacetic acid.
Uses
The present disclosure provides methods and compositions for transport and/or delivery of a cargo molecule to certain location(s) within a cell (e.g., a supranuclear location) or across a cell (e.g., epithelial cell), either in vitro or in vivo (e.g., in a rodent or a human). Such cargo can be directed to a set of location(s) by coupling it to a carrier molecule. Such carrier molecule can interact with unique receptors both on the cell surface and intracellularly for the targeted delivery of the cargo. Various such carrier, cargos, and uses thereof are described herein.
Contemplated herein are delivery constructs that can be used to deliver a cargo to a location within a cell (e.g., epithelial cell) or across a cell (e.g., epithelial cell). Such carriers can be a small molecule, a polypeptide, an aptamer, an antibody, a nucleic acid a fragment of any of the above, or a combination of any of the above. The delivery constructs described herein can be used for various applications, including but not limited to, therapeutic, preventative, and/or diagnostic applications. Such therapeutic, preventative, and/or diagnostic applications can be provided if, for example, therapeutically active cargo molecules are coupled to carriers described herein that enable targeted delivery to various locations (e.g., in a subject such as a human).
Pharmaceutical Compositions and Delivery Methods
The pharmaceutical compositions of the present disclosure relate to compositions for administration to a human subject. The pharmaceutical compositions comprise the non-naturally occurring delivery constructs recited herein, alone or in combination. The pharmaceutical compositions can comprise additional molecules capable of altering the characteristics of the non-naturally occurring delivery constructs, for example, stabilizing, modulating and/or activating their function. The composition may, e.g., be in solid or liquid form and can be, inter alia, in the form of (a) powder(s), (a) tablet(s), (a) solution(s) or (an) aerosol(s). The pharmaceutical composition of the present disclosure may, optionally and additionally, comprise a pharmaceutically acceptable carrier. “Pharmaceutically acceptable carrier” refers to a non-toxic solid, semisolid or liquid filler, diluent, encapsulating material and any of the standard pharmaceutical carriers, vehicles, buffers, and excipients, such as a phosphate buffered saline solution, 5% aqueous solution of dextrose, and emulsions, such as an oil/water or water/oil emulsion, and various types of wetting agents and/or adjuvants.
The pharmaceutical compositions are generally formulated appropriately for the immediate use intended for the delivery construct. For example, if the delivery construct is not to be administered immediately, the delivery construct can be formulated in a composition suitable for storage. One such composition is a lyophilized preparation of the delivery construct together with a suitable stabilizer. Alternatively, the delivery construct composition can be formulated for storage in a solution with one or more suitable stabilizers. Any such stabilizer known to one of skill in the art without limitation can be used. For example, stabilizers suitable for lyophilized preparations include, but are not limited to, sugars, salts, surfactants, proteins, chaotropic agents, lipids, and amino acids. Stabilizers suitable for liquid preparations include, but are not limited to, sugars, salts, surfactants, proteins, chaotropic agents, lipids, and amino acids. Specific stabilizers than can be used in the compositions include, but are not limited to, trehalose, serum albumin, phosphatidylcholine, lecithin, and arginine. Other compounds, compositions, and methods for stabilizing a lyophilized or liquid preparation of the delivery constructs can be found, for example, in U.S. Pat. Nos. 6,573,237, 6,525,102, 6,391,296, 6,255,284, 6,133,229, 6,007,791, 5,997,856, and 5,917,021.
In various embodiments, the pharmaceutical compositions of the present disclosure are formulated for oral delivery. The pharmaceutical compositions formulated for oral administration take advantage of the bacterial toxin's ability to mediate transcytosis across the gastrointestinal (GI) epithelium and/or delivery to the interior of a cell of the GI epithelium (e.g., gut). It is anticipated that oral administration of these pharmaceutical compositions will result in absorption of the delivery construct through polarized epithelial cells of the digestive mucosa, e.g., the intestinal mucosa, followed by release of the biologically active cargo at the basolateral side of the mucous membrane. In various embodiments, the epithelial cell is selected from the group consisting of nasal epithelial cells, oral epithelial cells, intestinal epithelial cells, rectal epithelial cells, vaginal epithelial cells, and pulmonary epithelial cells. Pharmaceutical compositions of the disclosure can include the addition of a transcytosis enhancer to facilitate transfer of the fusion protein across the GI epithelium. Such enhancers are known in the art. See Xia et al., (2000) J. Pharmacol. Experiment. Therap., 295:594-600; and Xia et al. (2001) Pharmaceutical Res., 18(2):191-195, each incorporated by reference in its entirety herein.
Without being bound to any theory, it is assumed that once transported across the GI epithelium, the delivery constructs of the disclosure will exhibit extended half-life in serum, that is, the biologically active cargo of the delivery constructs will exhibit an extended serum half-life compared to the biologically active cargo in its non-fused state. As such, the oral formulations of the pharmaceutical compositions of the present disclosure are prepared so that they are suitable for transport to the GI epithelium and protection of the delivery construct in the stomach. Such formulations can include carrier and dispersant components and can be in any suitable form, including aerosols (for oral or pulmonary delivery), syrups, elixirs, tablets, including chewable tablets, hard or soft capsules, troches, lozenges, aqueous or oily suspensions, emulsions, cachets or pellets granulates, and dispersible powders. In various embodiments, the pharmaceutical compositions are employed in solid dosage forms, e.g., tablets, capsules, or the like, suitable for simple oral administration of precise dosages.
The oral formulation can comprise a delivery construct and one or more compounds that can protect the delivery construct while it is in the stomach. For example, the protective compound should be able to prevent acid and/or enzymatic hydrolysis of the delivery construct. In various embodiments, the oral formulation comprises a delivery construct and one or more compounds that can facilitate transit of the construct from the stomach to the small intestine. The one or more compounds that can protect the delivery construct from degradation in the stomach can also facilitate transit of the construct from the stomach to the small intestine. For example, inclusion of sodium bicarbonate can be useful for facilitating the rapid movement of intra-gastric delivered materials from the stomach to the duodenum as described in Mrsny et al., Vaccine 17:1425-1433, 1999. Other methods for formulating compositions so that the delivery constructs can pass through the stomach and contact polarized epithelial membranes in the small intestine include, but are not limited to, enteric-coating technologies as described in DeYoung, Int J Pancreatol, 5 Suppl: 31-6, 1989 and the methods provided in U.S. Pat. Nos. 6,613,332, 6,174,529, 6,086,918, 5,922,680, and 5,807,832, each incorporated by reference in its entirety herein.
Pharmaceutical compositions intended for oral use can be prepared according to any method known to the art for the manufacture of pharmaceutical compositions and such compositions can contain one or more agents selected from the group consisting of sweetening agents in order to provide a pharmaceutically elegant and palatable preparation. For example, to prepare orally deliverable tablets, the delivery construct is mixed with at least one pharmaceutical excipient, and the solid formulation is compressed to form a tablet according to known methods, for delivery to the gastrointestinal tract. The tablet composition is typically formulated with additives, e.g. a saccharide or cellulose carrier, a binder such as starch paste or methyl cellulose, a filler, a disintegrator, or other additives typically usually used in the manufacture of medical preparations. To prepare orally deliverable capsules, DHEA is mixed with at least one pharmaceutical excipient, and the solid formulation is placed in a capsular container suitable for delivery to the gastrointestinal tract. Compositions comprising delivery constructs can be prepared as described generally in Remington's Pharmaceutical Sciences, 18th Ed. 1990 (Mack Publishing Co. Easton Pa. 18042) at Chapter 89, which is herein incorporated by reference.
The pharmaceutical compositions can be formulated as orally deliverable tablets containing delivery constructs in admixture with non-toxic pharmaceutically acceptable excipients, which are suitable for manufacture of tablets. These excipients can be inert diluents, such as calcium carbonate, sodium carbonate, lactose, calcium phosphate or sodium phosphate; granulating and disintegrating agents, for example, maize starch, gelatin or acacia, and lubricating agents, for example, magnesium stearate, stearic acid, or talc. The tablets can be uncoated or they can be coated with known techniques to delay disintegration and absorption in the gastrointestinal track and thereby provide a sustained action over a longer period of time. For example, a time delay material such as glyceryl monostearate or glyceryl distearate alone or with a wax can be employed.
The pharmaceutical compositions can be formulated as hard gelatin capsules wherein the delivery construct is mixed with an inert solid diluent, for example, calcium carbonate, calcium phosphate, or kaolin or as soft gelatin capsules wherein the delivery construct is mixed with an aqueous or an oil medium, for example, arachis oil, peanut oil, liquid paraffin or olive oil.
Aqueous suspensions can contain a delivery construct in the admixture with excipients suitable for the manufacture of aqueous suspensions. Such excipients are suspending agents, for example, sodium carboxymethylcellulose, methylcellulose, hydroxypropylmethylcellulose, sodium alginate, polyvinylpyrrolidone, gum tragacanth and gum acacia; dispersing or wetting agents can be a naturally occurring phosphatide, for example, lecithin, or condensation products of an alkylene oxide with fatty acids, for example, polyoxyethylene stearate, or condensation products of ethylene oxide with long chain aliphatic alcohols, for example, heptadecylethyloxycetanol, or condensation products of ethylene oxide with partial esters derived from fatty acids and a hexitol such as polyoxyethylene sorbitol monooleate, or condensation products of ethylene oxide with partial esters derived from fatty acids and hexitol anhydrides, for example polyoxyethylene sorbitan monooleate. The aqueous suspensions can also contain one or more preservatives for example, ethyl or n-propyl p-hydroxybenzoate, one or more coloring agents, one or more flavoring agents and one or more sweetening agents such as sucrose or saccharin.
Oily suspensions can be formulated by suspending the delivery construct in a vegetable oil, for example, arachis oil, olive oil, sesame oil or coconut oil, or in a mineral oil such as liquid paraffin. The oil suspensions can contain a thickening agent, for example, beeswax, hard paraffin or cetyl alcohol. Sweetening agents, such as those set forth above, and flavoring agents can be added to provide a palatable oral preparation. These compositions can be preserved by the addition of an antioxidant such as ascorbic acid.
The pharmaceutical compositions can be in the form of oil-in-water emulsions. The oil phase can be a vegetable oil, for example, olive oil or arachis oil, or a mineral oil for example, gum acacia or gum tragacanth, naturally-occurring phosphatides, for example soybean lecithin, and esters or partial esters derived from fatty acids and hexitol anhydrides, for example, sorbitan monooleate, and condensation products of the same partial esters with ethylene oxide, for example, polyoxyethylene sorbitan monooleate. The emulsions can also contain sweetening and flavoring agents.
The pharmaceutical composition can be in the form of a tablet or capsule, and the tablet or capsule can be coated or encapsulated to protect a therapeutically or biologically active cargo from enzymatic action in the stomach and to ensure that there is sufficient biologically active cargo to be absorbed by the subject to produce an effective response. Such coating or encapsulation methods include, e.g., encapsulation in nanoparticles composed of polymers with a hydrophobic backbone and hydrophilic branches as drug carriers, encapsulation in microparticles, insertion into liposomes in emulsions, and conjugation to other molecules. In some cases, the capsule or tablet releases the delivery construct in a pH-dependent manner. Capsules or tablets used for administering a delivery construct as described herein can comprise one or more enteric coatings.
Examples of nanoparticles include mucoadhesive nanoparticles coated with chitosan and Carbopol (Takeuchi et al., Adv. Drug Deliv. Rev. 47(1):39-54, 2001) and nanoparticles containing charged combination polyesters, poly(2-sulfobutyl-vinyl alcohol) and poly(D,L-lactic-co-glycolic acid) (Jung et al., Eur. J. Pharm. Biopharm. 50(1):147-160, 2000).
Encapsulated or coated tablets can be used that release a biologically active cargo in a layer-by-layer manner, thereby releasing biologically active cargo over a pre-determined time frame while moving along the gastrointestinal tract. In addition, tablets comprising the biologically active cargo can be placed within a larger tablet, thereby protecting the inner tablet from environmental and processing conditions, such as temperature, chemical agents (e.g., solvents), pH, and moisture. The outer tablet and coatings further serve to protect the biologically active cargo in the gastric environment.
Pharmaceutical compositions described herein can be formulated for oral delivery using polyester microspheres, zein microspheres, proteinoid microspheres, polycyanoacrylate microspheres, and lipid-based systems (see, for example, DiBase and Morrel, Oral Delivery of Microencapsulated Proteins, in Protein Delivery: Physical Systems, Sanders and Hendren (eds.), pages 255-288 (Plenum Press 1997)).
Surface-active agents or surfactants promote absorption of polypeptides through mucosal membrane or lining. Useful surface-active agents or surfactants include fatty acids and salts thereof, bile salts, phospholipid, or an alkyl saccharide. Examples of fatty acids and salts thereof include sodium, potassium and lysine salts of caprylate (C8), caprate (C10), laurate (C12) and myristate (C14). Examples of bile salts include cholic acid, chenodeoxycholic acid, glycocholic acid, taurocholic acid, glycochenodeoxycholic acid, taurochenodeoxycholic acid, deoxycholic acid, glycodeoxycholic acid, taurodeoxycholic acid, lithocholic acid, and ursodeoxycholic acid. Examples of phospholipids include single-chain phospholipids, such as lysophosphatidylcholine, lysophosphatidylglycerol, lysophosphatidylethanolamine, lysophosphatidylinositol and lysophosphatidylserine; or double-chain phospholipids, such as diacylphosphatidylcholines, diacylphosphatidylglycerols, diacylphosphatidylethanolamines, diacylphosphatidylinositols and diacylphosphatidylserines. Examples of alkyl saccharides include alkyl glucosides or alkyl maltosides, such as decyl glucoside and dodecyl maltoside.
The present disclosure relates to methods and compositions that allow orally administering the pharmaceutical compositions of the disclosure. Without intending to be bound to any particular theory or mechanism of action, it is believed that oral administration of the delivery constructs results in absorption of the delivery construct through polarized epithelial cells of the digestive mucosa, e.g., the intestinal mucosa, followed by cleavage of the delivery construct and release of the biologically active cargo at the basolateral side of the mucous membrane. Thus, when the biologically active cargo exerts a biological activity in the liver, such as, for example, activities mediated by IL-10 binding to its cognate receptor, the biologically active cargo is believed to exert an effect in excess of what would be expected based on the plasma concentrations observed in the subject, i.e., oral administration of the delivery construct can deliver a higher effective concentration of the delivered biologically active cargo to the liver of the subject than is observed in the subject's plasma.
The present disclosure relates to methods of orally administering the pharmaceutical compositions of the disclosure. Such methods can include, but are not limited to, steps of orally administering the compositions by the patient or a caregiver. Such administration steps can include administration on intervals such as once or twice per day depending on the delivery construct, disease or patient condition or individual patient. Such methods also include the administration of various dosages of the individual delivery construct. For instance, the initial dosage of a pharmaceutical composition can be at a higher level to induce a desired effect, such as reduction in blood glucose levels. Subsequent dosages can then be decreased once a desired effect is achieved. Such changes or modifications to administration protocols can be performed by the attending physician or health care worker.
These pharmaceutical compositions can be administered to the subject at a suitable dose. The dosage regimen can be determined by the attending physician based upon specific clinical factors. As is well known in the medical arts, dosages for any one patient depend upon many factors, including the patient's size, body surface area, age, the particular compound to be administered, sex, time and route of administration, general health, and other drugs being administered concurrently. The therapeutically effective amount for a given situation will readily be determined by routine experimentation and is within the skills and judgment of the ordinary clinician or physician. The skilled person knows that the effective amount of a pharmaceutical composition administered to an individual will, inter alia, depend on the nature of the biologically active cargo. The length of treatment needed to observe changes and the interval following treatment for responses to occur vary depending on the desired effect. The particular amounts can be determined by conventional tests, which are well known to the person skilled in the art.
The amount of biologically active cargo is an amount effective to accomplish the purpose of the particular active agent. The amount in the composition typically is a pharmacologically, biologically, therapeutically, or chemically effective amount. However, the amount can be less than a pharmacologically, biologically, therapeutically, or chemically effective amount when the composition is used in a dosage unit form, such as a capsule, a tablet or a liquid, because the dosage unit form can contain a multiplicity of carrier/biologically or chemically active agent compositions or can contain a divided pharmacologically, biologically, therapeutically, or chemically effective amount. The total effective amounts can then be administered in cumulative units containing, in total, pharmacologically, biologically, therapeutically or chemically active amounts of biologically active cargo.
As used herein, the terms “co-administration”, “co-administered” and “in combination with”, referring to the delivery constructs of the disclosure and one or more other therapeutic agents, is intended to mean, and does refer to and include the following: simultaneous administration of such combination of delivery constructs of the disclosure and therapeutic agent(s) to a patient in need of treatment, when such components are formulated together into a single dosage form which releases said components at substantially the same time to said patient; substantially simultaneous administration of such combination of delivery constructs of the disclosure and therapeutic agent(s) to a patient in need of treatment, when such components are formulated apart from each other into separate dosage forms which are taken at substantially the same time by said patient, whereupon said components are released at substantially the same time to said patient; sequential administration of such combination of delivery constructs of the disclosure and therapeutic agent(s) to a patient in need of treatment, when such components are formulated apart from each other into separate dosage forms which are taken at consecutive times by said patient with a significant time interval between each administration, whereupon said components are released at substantially different times to said patient; and sequential administration of such combination of delivery constructs of the disclosure and therapeutic agent(s) to a patient in need of treatment, when such components are formulated together into a single dosage form which releases said components in a controlled manner whereupon they are released in a concurrent, consecutive, and/or overlapping manner at the same and/or different times to said patient, where each part can be administered by either the same or a different route.
A combination therapy can comprise administering the isolated delivery construct composition and the second agent composition simultaneously, either in the same pharmaceutical composition or in separate pharmaceutical compositions. In various embodiments, isolated delivery construct composition and the second agent composition are administered sequentially, i.e., the isolated delivery construct composition is administered either prior to or after the administration of the second agent composition.
An administration of the isolated delivery construct composition and the second agent composition can be concurrent, i.e., the administration period of the isolated delivery construct composition and the second agent composition overlap with each other.
An administration of the isolated delivery construct composition and the second agent composition can be non-concurrent. For example, in various embodiments, the administration of the isolated delivery construct composition is terminated before the second agent composition is administered. The administration second agent composition can be terminated before the isolated delivery construct composition is administered.
Methods of Treatment
The pharmaceutical compositions formulated for oral delivery can be used to treat certain classes of diseases or medical conditions that are particularly amenable for oral formulation and delivery. Such classes of diseases or conditions include, e.g., viral disease or infections, cancer, a metabolic disease, obesity, autoimmune diseases, inflammatory diseases, allergy, graft-vs-host disease, systemic microbial infection, anemia, cardiovascular disease, psychosis, genetic diseases, neurodegenerative diseases, disorders of hematopoietic cells, diseases of the endocrine system or reproductive systems, gastrointestinal diseases. In many chronic diseases, oral formulations of the delivery constructs of the disclosure are particularly useful because they allow long-term patient care and therapy via home oral administration without reliance on injectable treatment or drug protocols.
A pharmaceutical composition of the present disclosure can comprise any of the delivery constructs described herein, which includes any combination of carrier, cargo, and/or spacer described herein. Specifically, the delivery constructs described herein allow for oral administration, which can be followed by transport of the delivery construct across or into a cell of an epithelium of a subject. A delivery construct that has been transported across such an epithelial layer can subsequently reach various parts and/or organs and/or tissues within the subject. A delivery construct, and in various cases the cargo that a delivery construct comprises, can elicit an effect upon reaching a submucosal compartment. For example, a biologically active cargo can be a cargo capable of eliciting an immune response, and thus a delivery construct can present such cargo to immune cell once it has reached a submucosal compartment.
The present disclosure relates to methods for treatment, prophylaxis and/or prevention of an inflammatory disease in a subject, comprising administering a pharmaceutical composition of the present disclosure to the subject. “Inflammatory diseases” include all diseases associated with acute or chronic inflammation. Acute inflammation is the initial response of the body to harmful stimuli and results from an increased movement of plasma and leukocytes (such as e.g. granulocytes) from the blood into the injured tissues. A number of biochemical events propagates and matures the inflammatory response, involving the local vascular system, the immune system, and various cells within the injured tissue. Prolonged inflammation is referred to as chronic inflammation, which leads to a progressive shift in the type of cells present at the site of inflammation and is characterized by simultaneous destruction and healing of the tissue from the inflammatory process. Inflammatory diseases can be caused by e.g. burns, chemical irritants, frostbite, toxins, infection by pathogens, physical injury, immune reactions due to hypersensitivity, ionizing radiation, or foreign bodies, such as e.g. splinters, dirt and debris. Examples of inflammatory diseases are well known in the art.
An inflammatory disease can be selected from the group consisting of inflammatory bowel disease, psoriasis and bacterial sepsis. The term “inflammatory bowel disease”, as used herein, refers to a group of inflammatory conditions of the colon and small intestine including, for example, Crohn's disease, ulcerative colitis, collagenous colitis, lymphocytic colitis, ischemic colitis, diversion colitis, Behcet's syndrome and indeterminate colitis. Delivery constructs that can be used to prevent and/or treat such inflammatory disease include those comprising the amino acid sequence set forth in SEQ ID NO: 154 and/or SEQ ID NO: 155.
“Crohn's disease”, in accordance with the present disclosure, is a T-helper Type 1 (Th1) inflammatory bowel disease, which has an immune response pattern that includes an increased production of interleukin-12, tumor necrosis factor (TNF), and interferon-γ (Romagnani. Inflamm Bowel Dis 1999; 5:285-94), and which can have a devastating impact on the lifestyle of a patient afflicted therewith. Common symptoms of Crohn's disease include diarrhea, cramping, abdominal pain, fever, and even rectal bleeding. Crohn's disease and complications associated with it often results in the patient requiring surgery, often more than once. There is no known cure for Crohn's disease, and long-term, effective treatment options are limited. The goals of treatment are to control inflammation, correct nutritional deficiencies, and relieve symptoms like abdominal pain, diarrhea, and rectal to bleeding. While treatment can help control the disease by lowering the number of times a person experiences a recurrence, there is no cure. Treatment can include drugs, nutrition supplements, surgery, or a combination of these options. Common treatments which can be administered for treatment include anti-inflammation drugs, including sulfasalazine, cortisone or steroids, including prednisone, immune system suppressors, such as 6-mercaptopurine or azathioprine, and antibiotics.
“Psoriasis”, in accordance with the present disclosure, is a disease, which affects the skin and joints. It commonly causes red scaly patches to appear on the skin. The scaly patches caused by psoriasis, called psoriatic plaques, are areas of inflammation and excessive skin production. Skin rapidly accumulates at these sites and takes a silvery-white appearance. Plaques frequently occur on the skin of the elbows and knees, but can affect any area including the scalp and genitals. Psoriasis is hypothesized to be immune-mediated and is not contagious. The disorder is a chronic recurring condition, which varies in severity from minor localized patches to complete body coverage. Fingernails and toenails are frequently affected (psoriatic nail dystrophy)—and can be seen as an isolated finding. Psoriasis can also cause inflammation of the joints, which is known as psoriatic arthritis. Ten to fifteen percent of people with psoriasis have psoriatic arthritis.
The term “bacterial sepsis”, as used herein, refers to life-threatening conditions resulting from the circulation of bacteria in the blood stream. Sepsis results in generalized systemic production of pro-inflammatory cytokines that results in tissue damage and ultimately septic shock due to failure of the microcirculation.
The present disclosure relates to methods for treatment, prophylaxis and/or prevention of an autoimmune disease in a subject, comprising administering a pharmaceutical composition of the present disclosure to the subject. An autoimmune disease, as pertains to the present disclosure, is a disease or disorder arising from and directed against an individual's own tissues or a co-segregate or manifestation thereof or resulting condition therefrom. In various embodiments. the autoimmune disease is selected from the group consisting of systemic lupus erythematosus (SLE), pemphigus vulgaris, myasthenia gravis, hemolytic anemia, thrombocytopenia purpura, Grave's disease, Sjogren's disease, dermatomyositis, Hashimoto's disease, polymyositis, inflammatory bowel disease, multiple sclerosis (MS), diabetes mellitus, rheumatoid arthritis, and scleroderma. Exemplary delivery constructs that can be used to treat those disease can include those comprising any carrier set forth in SEQ ID NO: 4-SEQ ID NO: 125 coupled to, for example, an anti-TNFa antibody, or a functional binding fragment thereof.
“Rheumatoid arthritis”, in accordance with the present disclosure, is an autoimmune disorder that causes the body's immune system to attack the bone joints (Muller B et al., Springer Semin. Immunopathol., 20:181-96, 1998). Rheumatoid arthritis is a chronic, systemic inflammatory disorder that can affect many tissues and organs, but principally attacks synovial joints. The process produces an inflammatory response of the synovium (synovitis) secondary to hyperplasia of synovial cells, excess synovial fluid, and the development of pannus in the synovium. The pathology of the disease process often leads to the destruction of articular cartilage and ankylosis of the joints. Rheumatoid arthritis can also produce diffuse inflammation in the lungs, pericardium, pleura, and sclera, and also nodular lesions, most common in subcutaneous tissue under the skin.
The present disclosure relates to methods and compositions for treatment, prophylaxis and/or prevention of a cancer in a subject, comprising administering a pharmaceutical composition of the present disclosure to the subject. Cancers to be treated include, but are not limited to, non-Hodgkin's lymphomas, Hodgkin's lymphoma, chronic lymphocytic leukemia, hairy cell leukemia, acute lymphoblastic leukemia, multiple myeloma, carcinomas of the pancreas, colon, gastric intestine, prostate, bladder, kidney ovary, cervix, breast, lung, nasopharynx, malignant melanoma and rituximab resistant NHL and leukemia.
The therapeutically effective amount of a pharmaceutical composition of the present disclosure will be administered in combination with one or more other therapeutic agents. Such therapeutic agents can be accepted in the art as a standard treatment for a particular disease state as described herein, such as inflammatory disease, autoimmune disease, or cancer. Exemplary therapeutic agents contemplated include, but are not limited to, cytokines, growth factors, steroids, NSAIDs, DMARDs, anti-inflammatories, chemotherapeutics, radiotherapeutics, or other active and ancillary agents.
The present disclosure relates to methods for treatment, prophylaxis and/or prevention of a metabolic disorder in a subject, comprising administering a pharmaceutical composition of the present disclosure to the subject. In various embodiments, the metabolic disorder is selected from the group consisting of: diabetes, obesity, diabetes as a consequence of obesity, hyperglycemia, dyslipidemia, hypertriglyceridemia, syndrome X, insulin resistance, impaired glucose tolerance (IGT), diabetic dyslipidemia, and hyperlipidemia.
The present disclosure relates to methods for treatment, prophylaxis and/or prevention of a fatty liver disease (e.g., nonalcoholic fatty liver disease (NAFLD); nonalcoholic steatohepatitis (NASH)), a gastrointestinal disease, or a neurodegenerative disease in a subject, comprising administering a pharmaceutical composition of the present disclosure to the subject.
The present disclosure relates to methods and compositions for treatment, prophylaxis and/or prevention of a GH deficient growth disorder in a subject, said method comprising administering a pharmaceutical composition of the present disclosure to the subject. In various embodiments, the disorder is selected from the group consisting of: growth hormone deficiency (GHD), Turner syndrome (TS), Noonan syndrome, Prader-Willi syndrome, short stature homeobox-containing gene (SHOX) deficiency, chronic renal insufficiency, and idiopathic short stature short bowel syndrome, GH deficiency due to rare pituitary tumors or their treatment, and muscle-wasting disease associated with HIV/AIDS.
A subject of the present disclosure can be a human or a rodent. The subject can be a human. A subject can be affected by one or more of the following: inflammatory bowel disease, psoriasis, bacterial sepsis, systemic lupus erythematosus (SLE), pemphigus vulgaris, myasthenia gravis, hemolytic anemia, thrombocytopenia purpura, Grave's disease, Sjogren's disease, dermatomyositis, Hashimoto's disease, polymyositis, inflammatory bowel disease, multiple sclerosis (MS), diabetes mellitus, rheumatoid arthritis, scleroderma, non-Hodgkin's lymphomas, Hodgkin's lymphoma, chronic lymphocytic leukemia, hairy cell leukemia, acute lymphoblastic leukemia, multiple myeloma, carcinomas of the bladder, kidney ovary, cervix, breast, lung, nasopharynx, malignant melanoma, rituximab resistant NHL or leukemia, diabetes, obesity, diabetes as a consequence of obesity, hyperglycemia, dyslipidemia, hypertriglyceridemia, syndrome X, insulin resistance, impaired glucose tolerance (IGT), diabetic dyslipidemia, hyperlipidemia, growth hormone deficiency (GHD), Turner syndrome (TS), Noonan syndrome, Prader-Willi syndrome, short stature homeobox-containing gene (SHOX) deficiency, chronic renal insufficiency, or idiopathic short stature short bowel syndrome.
The methods and compositions described herein can also be used to diagnose disease or condition. Diagnosing a disease or condition can include invasive and non-invasive diagnostic modalities. Specifically, the compositions described herein can be used to non-invasively diagnose a disease, e.g., by measuring the expression of a certain marker (e.g., a biomarker) or antigen. Such diagnoses can be conducted by coupling a cargo to a carrier, wherein the cargo can have a binding affinity for a certain marker (e.g., a biomolecule representative which presence or concentration in a certain organ, tissue, or cell is representative of a certain disease or condition). Diagnoses as described herein can further comprise monitoring a response to a treatment (e.g., the treatment of a subject). For example, if response to a treatment correlates with a reduction of a certain marker (e.g., a biomarker), the delivery constructs of the present disclosure can be used to measure such marker at a certain location (e.g., a certain immune cell population in a submucosal compartment). In addition to non-invasive diagnoses, the methods and compositions described herein can be used to provide biologically and/or therapeutically relevant information, e.g., upon a biopsy sample has been taken from a subject, which can be followed by immunohistochemistry, e.g., the detection of accumulation of a delivery constructs in a certain tissue etc.
Non-invasive diagnosis can comprise molecular and/or nuclear imaging. For example, a delivery construct can comprise cargo that is labeled with a fluorescent and/or radioactive compound such that the location and/or concentration of such a delivery construct can be determined in a subject after administration. Any moiety with diagnostic applicability as described herein can be used to provide diagnostic and/or theranostic (therapeutic and diagnostic) agents.
Polynucleotides Encoding Delivery constructs
The methods and compositions of the present disclosure provides polynucleotides comprising a nucleotide sequence encoding non-naturally occurring delivery constructs and/or hybrid delivery construct polypeptides. These polynucleotides are useful, for example, for making the delivery constructs and/or hybrid delivery construct polypeptides. The disclosure provides an expression system that comprises a recombinant polynucleotide sequence encoding a bacterial carrier receptor binding domain, and a polyspacer insertion site for a polynucleotide sequence encoding a biologically active cargo. The polyspacer insertion site can be anywhere in the polynucleotide sequence so long as the polyspacer insertion does not disrupt the delivery construct of the bacterial toxin. The expression system can comprise a polynucleotide sequence that encodes a cleavable spacer so that cleavage at the cleavable spacer separates a biologically active cargo encoded by a nucleic acid inserted into the polyspacer insertion site from the remainder of the encoded delivery construct. Thus, in embodiments where the polyspacer insertion site is at an end of the encoded construct, the polynucleotide comprises one nucleotide sequence encoding a cleavable spacer between the polyspacer insertion site and the remainder of the polynucleotide. In embodiments where the polyspacer insertion site is not at the end of the encoded construct, the polyspacer insertion site can be flanked by nucleotide sequences that each encode a cleavable spacer.
Various in vitro methods that can be used to prepare a polynucleotide encoding a delivery construct useful in the delivery constructs of the disclosure include, but are not limited to, reverse transcription, the polymerase chain reaction (PCR), the ligase chain reaction (LCR), the transcription-based amplification system (TAS), the self-sustained sequence replication system (3 SR) and the QP replicase amplification system (QB). Any such technique known by one of skill in the art to be useful in construction of recombinant nucleic acids can be used. For example, a polynucleotide encoding the protein or a portion thereof can be isolated by polymerase chain reaction of cDNA using primers based on the DNA sequence of a delivery construct or a nucleotide encoding the receptor binding domain.
Guidance for using these cloning and in vitro amplification methodologies are described in, for example, U.S. Pat. No. 4,683,195; Mullis et al., 1987, Cold Spring Harbor Symp. Quant. Biol. 51:263; and Erlich, ed., 1989, PCR Technology, Stockton Press, NY. Polynucleotides encoding a delivery construct, or a portion thereof, also can be isolated by screening genomic of cDNA libraries using probes selected from the sequences of the desired polynucleotide under stringent, moderately stringent, or highly stringent hybridization conditions.
Further, the polynucleotides can also encode a secretory sequence at the amino terminus of the encoded delivery construct. Such constructs are useful for producing the delivery constructs in mammalian cells as they simplify isolation of the delivery construct and/or hybrid delivery construct polypeptides.
Furthermore, the polynucleotides of the disclosure also encompass derivative versions of polynucleotides encoding a delivery construct. Such derivatives can be made by any method known by one of skill in the art without limitation. For example, derivatives can be made by site-specific mutagenesis, including substitution, insertion, or deletion of one, two, three, five, ten or more nucleotides, of polynucleotides encoding the delivery construct. Alternatively, derivatives can be made by random mutagenesis. One method for randomly mutagenizing a nucleic acid comprises amplifying the nucleic acid in a PCR reaction in the presence of 0.1 mM MnCl2 and unbalanced nucleotide concentrations. These conditions increase the inaccuracy incorporation rate of the polymerase used in the PCR reaction and result in random mutagenesis of the amplified nucleic acid.
Accordingly, the disclosure provides a polynucleotide that can encode one or more delivery constructs. A delivery construct comprises a bacterial carrier and a biologically active cargo to be delivered to a subject; and, optionally, a non-cleavable or cleavable spacer. Cleavage at the cleavable spacer can separate the biologically active cargo from the remainder of the delivery construct. The cleavable spacer can be cleaved by an enzyme that is present at a basolateral membrane of a polarized epithelial cell of the subject or in the plasma of the subject.
The polynucleotide can hybridize under stringent hybridization conditions to any polynucleotide of this disclosure. The polynucleotide can hybridize under stringent conditions to a nucleic acid that encodes any delivery construct of the disclosure.
The disclosure provides expression vectors for expressing the delivery constructs and/or hybrid delivery construct polypeptides. Generally, expression vectors are recombinant polynucleotide molecules comprising expression control sequences operatively linked to a nucleotide sequence encoding a polypeptide. Expression vectors can readily be adapted for function in prokaryotes or eukaryotes by inclusion of appropriate promoters, replication sequences, selectable markers, etc. to result in stable transcription and translation or mRNA. Techniques for construction of expression vectors and expression of genes in cells comprising the expression vectors are well known in the art. See, e.g., Sambrook et al., 2001, Molecular Cloning—A Laboratory Manual, 3rd edition, Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y., and Ausubel et al., eds., Current Edition, Current Protocols in Molecular Biology, Greene Publishing Associates and Wiley Interscience, NY.
Useful promoters for use in expression vectors include, but are not limited to, a metallothionein promoter, a constitutive adenovirus major late promoter, a dexamethasone-inducible MMTV promoter, a SV40 promoter, a MRP pol III promoter, a constitutive MPSV promoter, a tetracycline-inducible CMV promoter (such as the human immediate-early CMV promoter), and a constitutive CMV promoter.
The expression vectors should contain expression and replication signals compatible with the cell in which the delivery constructs are expressed. Expression vectors useful for expressing delivery constructs include viral vectors such as retroviruses, adenoviruses and adeno-associated viruses, plasmid vectors, cosmids, and the like. Viral and plasmid vectors are preferred for transfecting the expression vectors into mammalian cells. For example, the expression vector pcDNA1 (Invitrogen, San Diego, Calif.), in which the expression control sequence comprises the CMV promoter, provides good rates of transfection and expression into such cells.
The expression vectors can be introduced into the cell for expression of the delivery constructs by any method known to one of skill in the art without limitation. Such methods include, but are not limited to, e.g., direct uptake of the molecule by a cell from solution; facilitated uptake through lipofection using, e.g., liposomes or immunoliposomes; particle-mediated transfection; etc. See, e.g., U.S. Pat. No. 5,272,065; Goeddel et al., eds, 1990, Methods in Enzymology, vol. 185, Academic Press, Inc., CA; Krieger, 1990, Gene Transfer and Expression—A Laboratory Manual, Stockton Press, NY; Sambrook et al., 1989, Molecular Cloning—A Laboratory Manual, Cold Spring Harbor Laboratory, NY; and Ausubel et al., eds., Current Edition, Current Protocols in Molecular Biology, Greene Publishing Associates and Wiley Interscience, NY.
The expression vectors can also contain a purification moiety that simplifies isolation of the delivery construct and/or hybrid delivery construct polypeptides. For example, a polyhistidine moiety of, e.g., six histidine residues, can be incorporated at the amino terminal end of the protein. The polyhistidine moiety allows convenient isolation of the protein in a single step by nickel-chelate chromatography. In various embodiments, the purification moiety can be cleaved from the remainder of the delivery construct following purification. In other embodiments, the moiety does not interfere with the function of the functional domains of the delivery construct and thus need not be cleaved.
The present disclosure provides a cell that can comprise an expression vector for expression of the delivery constructs and/or hybrid delivery construct polypeptides, or portions thereof. The cell can be selected for its ability to express high concentrations of the delivery construct to facilitate purification of the protein. In various embodiments, the cell is a prokaryotic cell, for example, E. coli. As described in the examples, the delivery constructs are properly folded and comprise the appropriate disulfide linkages when expressed in E. coli. The cell is a eukaryotic cell. Useful eukaryotic cells include yeast and mammalian cells. Any mammalian cell known by one of skill in the art to be useful for expressing a recombinant polypeptide, without limitation, can be used to express the delivery constructs. For example, Chinese hamster ovary (CHO) cells can be used to express the delivery constructs. The delivery constructs and/or hybrid delivery construct polypeptides of the disclosure can be produced by recombination, as described below. However, the delivery constructs can also be produced by chemical synthesis using methods known to those of skill in the art.
The delivery constructs of the present disclosure can be produced using a variety of methods. The selection of a production method can depend on the molecular structure of the delivery construct and/or its components (e.g., the carrier, cargo, and/or spacer). Thus, for some delivery constructs organic synthetic methods may be advantageous for producing such delivery construct. A delivery construct of the present disclosure can be a polypeptide. Such polypeptides can be produced, for example, using recombinant DNA methodology. Generally, this involves creating a DNA sequence that encodes the delivery construct, placing the DNA in an expression cassette under the control of a particular promoter, expressing the molecule in a host, isolating the expressed molecule and, if required, folding of the molecule into an active conformational form.
DNA encoding the delivery constructs described herein can be prepared by any suitable method, including, for example, cloning and restriction of appropriate sequences or direct chemical synthesis by methods such as the phosphotriester method of Narang et al. (1979) Meth. Enzymol. 68: 90-99; the phosphodiester method of Brown et al. (1979) Meth. Enzymol. 68: 109-151; the diethylphosphoramidite method of Beaucage et al. (1981) Tetra. Lett., 22: 1859-1862); the solid support method of U.S. Pat. No. 4,458,066, and the like.
Chemical synthesis produces a single stranded oligonucleotide. This can be converted into double stranded DNA by hybridization with a complementary sequence or by polymerization with a DNA polymerase using the single strand as a template. One of skill would recognize that while chemical synthesis of DNA is limited to sequences of about 100 bases, longer sequences can be obtained by the ligation of shorter sequences.
Alternatively, subsequences can be cloned and the appropriate subsequences cleaved using appropriate restriction enzymes. The fragments can then be ligated to produce the desired DNA sequence. A DNA encoding a delivery constructs of the present disclosure can be cloned using DNA amplification methods such as polymerase chain reaction (PCR). Thus, for example, the gene for the biologically active cargo is PCR amplified, using a sense primer containing the restriction site for, e.g., NdeI and an antisense primer containing the restriction site for HindIII. This can produce a nucleic acid encoding the biologically active cargo sequence and having terminal restriction sites. A delivery construct having “complementary” restriction sites can similarly be cloned and then ligated to the biologically active cargo and/or to a spacer attached to the biologically active cargo. Ligation of the nucleic acid sequences and insertion into a vector produces a vector encoding the biologically active cargo joined to the bacterial carrier receptor binding domain. In various embodiments, DNA encoding delivery constructs of the present disclosure is artificially synthesized by, for example, solid-phase DNA synthesis.
The production methods described herein can be used to produce the delivery constructs of the present disclosure, or (functional) variants thereof. For example, a “Cholix” (also referred to herein as Cholix toxin or Cholix exotoxin) can encompass a variety of functional variants (e.g., a functional genus), wherein the functional variants can comprise one or more variations is their amino acid sequence relative to SEQ ID NO: 1 as disclosed herein. Thus, in the present disclosure, the Cholix toxin having the amino acid sequence set forth in SEQ ID NO: 1 is used as the reference sequence when referred to Cholix. However, as described herein, the present disclosure is not limited to the Cholix having the amino acid sequence set forth in SEQ ID NO: 1 but instead encompasses all Cholix variants that fall within the functional genus of Cholix. For example, a variant of the Cholix exotoxin with the amino acid sequence set forth in SEQ ID NI: 1 can be a Cholix exotoxin which amino acid sequence is set forth in SEQ ID NO: 2, wherein both variants are capable of carrying out the same functions, e.g., transcytosis across an epithelial cell, and interact with the same receptors, such as ribophilin 1, SEC24, CK-8, TMEM132, GRP75, ERGIC-53, and/or perlecan.
Moreover, the production method of a polypeptide can affect, to some degree, the amino acid sequence of such polypeptide (e.g., due to post-translational modifications). For example, a first carrier and a second carrier are produced in the same expression system (e.g., a bacterial expression system such as E. coli or a mammalian expression system such as a CHO cell). In other cases, and as described herein, a first carrier and a second carrier are produced in a different expression system (e.g., a bacterial or a mammalian expression system). Bacterial expression systems include E. coli, and mammalian expression systems include CHO cells, for example. A bacterially produced polypeptide can comprise an N-cap, wherein the N-cap can comprise one more modifications at the N-terminal of the polypeptide. An N-cap can comprise an N-terminal methionine residue. Examples of Cholix domain I derived carrier polypeptides that can be bacterially produced and that comprise such N-terminal methionine include those comprising the amino acid sequences set forth in SEQ ID NO: 5, SEQ ID NO: 7, SEQ ID NO: 9, SEQ ID NO: 11, SEQ ID NO: 31, SEQ ID NO: 107, and SEQ ID NO: 135.
Experimental Methods
Transcytosis Testing. The transcytosis function of the isolated delivery constructs can be tested as a function of the delivery construct's ability to pass through an epithelial membrane. Because transcytosis first requires binding to the epithelial cell, these assays can also be used to assess the function of the delivery construct of the delivery construct.
The delivery construct's transcytosis activity can be tested by any method known by one of skill in the art, without limitation. In various embodiments, transcytosis activity can be tested by assessing the ability of a delivery construct to enter a non-polarized cell to which it binds. In case of Cholix derived carrier, and without intending to be bound to any particular theory or mechanism of action, it is described herein that the transcytosis function that allows a delivery construct to pass through a polarized epithelial cell and the function to enter non-polarized cells resides in the same domain, i.e. the domain described herein as domain I. Thus, the delivery construct's ability to enter the cell can be assessed, for example, by detecting the physical presence of the construct in the interior of the cell. For example, the delivery construct can be labeled with, for example, a fluorescent marker, and the delivery construct exposed to the cell. Then, the cells can be washed, removing any delivery construct that has not entered the cell, and the amount of label remaining determined. Detecting the label in this traction indicates that the delivery construct has entered the cell.
The delivery construct's transcytosis ability can be tested by assessing the delivery construct's ability to pass through a polarized epithelial cell. For example, the delivery construct can be labeled with, for example, a fluorescent marker (e.g., RFP) and contacted to the apical membranes of a layer of epithelial cells. Fluorescence detected on the basolateral side of the membrane formed by the epithelial cells indicates that the transcytosis domain is functioning properly.
In vivo transcytosis can be tested using male Wistar rats. Male Wistar rats can be housed 3-5 per cage with a 12/12 h light/dark cycle and can be 225-275 g (approximately 6-8 weeks old) when placed on study. Experiments can be conducted during the light phase using a non-recovery protocol that uses continuous isoflurane anesthesia. A 4-5 cm midline abdominal incision that exposes mid-jejunum regions can be conducted. Stock solutions at 3.86×10−5M of test articles can be prepared in phosphate buffered saline (PBS), with 50 μL (per 250 g rat) being administered by intraluminal injection (ILI) using a 29-gauge needle. The injection site mesentery can then be marked with a permanent marker. At study termination, a 3-5 mm region that captured the marked intestine segment can be isolated and processed for microscopic assessment. In vivo experiments are performed in accordance with the U.K. Animals (Scientific Procedures) Act of 1986, the European Communities Council Directive of 1986 (86/609/EEC), and the University of Bath's ethical review procedures.
Cleavable Spacer Cleavage Testing. The function of the cleavable spacer can generally be tested in a cleavage assay. Any suitable cleavage assay known by one of skill in the art, without limitation, can be used to test the cleavable spacers. Both cell-based and cell-free assays can be used to test the ability of an enzyme to cleave the cleavable spacers.
An exemplary cell-free assay for testing cleavage of cleavable spacers comprises preparing extracts of polarized epithelial cells and exposing a labeled delivery construct bearing a cleavable spacer to the fraction of the extract that corresponds to membrane-associated enzymes. In such assays, the label can be attached to either the biologically active cargo to be delivered or to the remainder of the delivery construct. Among these enzymes are cleavage enzymes found near the basolateral membrane of a polarized epithelial cell, as described above. Cleavage can be detected, for example, by binding the delivery construct with, for example, an antibody and washing off unbound molecules. If label is attached to the biologically active cargo to be delivered, then little or no label should be observed on the molecule bound to the antibodies. Alternatively, the binding agent used in the assay can be specific for the biologically active cargo, and the remainder of the construct can be labeled. In either case, cleavage can be assessed.
Cleavage can also be tested using cell-based assays that test cleavage by polarized epithelial cells assembled on semi-permeable membranes. For example, a labeled delivery construct, or portion of a delivery construct comprising the cleavable spacer, can be contacted to either the apical or basolateral side of a monolayer of suitable epithelial cells, such as, for example, Caco-2 cells, under conditions that permit cleavage of the spacer. Cleavage can be detected by detecting the presence or absence of the label using a reagent that specifically binds the delivery construct, or portion thereof. For example, an antibody specific for the delivery construct can be used to bind a delivery construct comprising a label distal to the cleavable spacer in relation to the portion of the delivery construct bound by the antibody. Cleavage can then be assessed by detecting the presence of the label on molecules bound to the antibody. If cleavage has occurred, little or no label should be observed on the molecules bound to the antibody. By performing such experiments, enzymes that preferentially cleave at the basolateral membrane rather than the apical membrane can be identified, and, further, the ability of such enzymes to cleave the cleavable spacer in a delivery construct can be confirmed.
Further, cleavage can also be tested using a fluorescence reporter assay as described in U.S. Pat. No. 6,759,207. Briefly, in such assays, the fluorescence reporter is contacted to the basolateral side of a monolayer of suitable epithelial cells under conditions that allow the cleaving enzyme to cleave the reporter. Cleavage of the reporter changes the structure of the fluorescence reporter, changing it from a non-fluorescent configuration to a fluorescent configuration. The amount of fluorescence observed indicates the activity of the cleaving enzyme present at the basolateral membrane.
Further, cleavage can also be tested using an intra-molecularly quenched molecular probe, such as those described in U.S. Pat. No. 6,592,847. Such probes generally comprise a fluorescent moiety that emits photons when excited with light of appropriate wavelength and a quencher moiety that absorbs such photons when in close proximity to the fluorescent moiety. Cleavage of the probe separates the quenching moiety from the fluorescent moiety, such that fluorescence can be detected, thereby indicating that cleavage has occurred. Thus, such probes can be used to identify and assess cleavage by particular cleaving enzymes by contacting the basolateral side of a monolayer of suitable epithelial cells with the probe under conditions that allow the cleaving enzyme to cleave the probe. The amount of fluorescence observed indicates the activity of the cleaving enzyme being tested.
In Vivo Studies. Male Wistar rats, housed in groups of 3-5 per cage with a 12/12 h light/dark cycle, were 225-275 g (approximately 6-8 weeks old) when placed on study after an overnight fast. All experiments were conducted during the light phase and carried out using a non-recovery protocol that used continuous isoflurane anesthesia. A 4-5 cm midline abdominal incision was made to expose the small intestine (mid-jejunum to proximal ileum regions). Equimolar stock solutions of Exotoxin A (PE)-RPF or Cholix-RFP truncation chimeras prepared in phosphate buffered saline were injected intra-lumenally using a 29-gauge hypodermic needle in a volume of 200 μL/kg (or ˜50 μL per 250 g rat). The adjacent mesentery of each intra-lumenal injection site was marked with a permanent ink pen. At selected time internals, the animal was euthanized and a 3-5 mm region that captured the marked intestine segment was isolated. All experiments were performed in accordance with the U.K. Animals (Scientific Procedures) Act of 1986, the European Communities Council Directive of 1986 (86/609/EEC), and the University of Bath's ethical review procedures.
Microscopy. Isolated tissues were rinse briefly in ice-cold PBS and then fixed with 4% paraformaldehyde on ice prior to labeling with primary antibodies to Exotoxin A (PE), Cholix, or RFP. Tissue distribution of a fluorescent-labeled secondary antibody that recognized these primary antibodies was assessed using a Zeiss LSM 510 fluorescence microscope. DAPI (4′,6-diamidino-2-phenylindole) was used as a nuclear stain.
Immunohistochemistry. Rehydrate tissue slides in decreasing concentrations of ethanol. Slides are immersed in histoclear (x2), 100% ethanol, 90% ethanol, 80% ethanol, 70% ethanol and PBS for 5 minutes each. Boil slides in 10 mM sodium citrate (pH 6) for 10 minutes. Remove from boil and allow to cool for 20 minutes. Dry slide and add a wax border around each tissue section using an ImmEdge hydrophobic pen. Wash tissue sections by pipetting PBS directly onto tissue. Perform 3×5 minute washes. Permeabilise tissue by pipetting 0.2% Triton x-100 in PBS onto sections. Incubate at room temperature for 45 minutes. Wash 3×5 minutes with PBS. Block tissue sections by pipetting 2% BSA and 2% donkey serum in 0.1% Triton x-100 in PBS onto sections. Incubate for 2 hours at room temperature. Remove blocking solution and add primary antibodies. Dilute antibodies to required concentration in 0.05% Triton x-100 and 1% BSA in PBS. Incubate overnight at 4° C. Wash 3×5 minutes with PBS. Incubate with secondary antibodies. Dilute antibodies to required concentration in 0.05% Triton x-100 and 1% BSA in PBS. Incubate for 2 hours at room temperature. Wash 3×5 minutes with PBS. Incubate with 200 nM DAPI at room temperature for 45 minutes. Wash 3×5 minutes with PBS. Dehydrate tissue sections by immersing in 70% ethanol, 100% ethanol, histoclear and 100% ethanol for 5 minutes each. Place a drop of fluorshield mounting media on each tissue section and cover with a glass coverslip. Gently apply pressure to the coverslip to remove air bubbles. Allow mounting media to dry for 4 hours. Store slides at 4° C. and image using confocal fluorescent microscope.
Evaluation of Cholix Domain I Interacting Proteins. In order to identify Cholix and/or PE interacting partners (e.g., receptors, enzymes, etc.) and establish the vesicular compartments where they interact with Cholix or PE exotoxins (e.g., a domain I of those exotoxins or a truncated version thereof), a series of pull-downs can be performed to identify potential interaction partners that can be followed by in silico associations using surface plasmon resonance, in vitro transcytosis studies using polarized Caco-2 human intestinal epithelial cells where genetic knockdown of specific targets can be achieved, and in vivo transcytosis studies where Cholix elements and specific receptors can be co-localized in established vesicular structures. Without being bound to any theory, it is assumed that a transcytosis process can involve elements that are normally restricted within specific vesicular elements of polarized intestinal epithelial cells but can be recruited or “hijacked” by, e.g., Cholix domain I or truncated versions thereof, to leave the late endosome and avoid lysosomal degradation following apical receptor-mediated endocytosis.
The following examples merely illustrate the disclosure, and are not intended to limit the disclosure in any way.
This Example describes the exemplary preparation of delivery constructs comprising truncated Cholix carriers (truncation in domains II and/or Ib) and truncated PE carriers (truncation in domains II and/or Ib) conjoined to heterologous cargos. In this Example, various non-naturally occurring delivery constructs were prepared as a single amino acid sequence and comprising a modified Cholix carrier sequence and/or a modified PE carrier sequence, a polyglycine-serine peptide spacer sequence, and a heterologous cargo.
The following modified Cholix and/or PE carriers were prepared and used to prepare Constructs 1-12: 1) a modified Cholix carrier truncated at amino acid residue 425 of SEQ ID NO: 1 (Cholix425, SEQ ID NO: 129); 2) a modified Cholix carrier truncated at amino acid residue 415 of SEQ ID NO: 1 (Cholix415, SEQ ID NO: 130); 3) a modified Cholix carrier truncated at amino acid residue 397 of SEQ ID NO: 1 (Cholix397, SEQ ID NO: 131); 4) a modified Cholix carrier truncated at amino acid residue 386 of SEQ ID NO: 1 (Cholix386, SEQ ID NO: 132); 5) a modified Cholix carrier truncated at amino acid residue 291 of SEQ ID NO: 1 (Cholix291, SEQ ID NO: 133); 6) a modified Cholix carrier truncated at amino acid residue 265 of SEQ ID NO: 1 (Cholix265, SEQ ID NO: 4); 7) a modified PE carrier truncated at amino acid residue 404 of SEQ ID NO: 135 (PE404, SEQ ID NO: 141); 8) a modified PE carrier truncated at amino acid residue 395 of SEQ ID NO: 135 (PE395, SEQ ID NO: 142); 9) a modified PE carrier truncated at amino acid residue 375 of SEQ ID NO: 135 (PE375, SEQ ID NO: 143); 10) a modified PE carrier truncated at amino acid residue 364 of SEQ ID NO: 135 (PE364, SEQ ID NO: 144); 11) a modified PE carrier truncated at amino acid residue 277 of SEQ ID NO: 135 (PE277, SEQ ID NO: 145); and 12) a modified PE carrier truncated at amino acid residue 252 of SEQ ID NO: 135 (PE252, SEQ ID NO: 137). In each Construct 1-12, the polyglycine-serine peptide spacer GTGGS (SEQ ID NO: 201) was used to conjoin red fluorescent protein (RFP, SEQ ID NO: 220) at the C-terminus of each modified toxin. The RFP emulated the presence of a biologically active cargo.
Codon-optimized genes were obtained from a commercial source and cloned into the pET26(+) expression vector that was used to transform BL21(DE3) component E. coli cells using the manufacturer's suggested protocol. Clones were selected using Kanamycin/Agar plates incubate overnight at 37° C. Protein expression in fermented cultures of selected clones was achieved by 1 mM IPTG induction. Pelleted bacteria were lysed to collect inclusion bodies that were extensively washed in 50 mM Tris, 20 mM EDTA, 2.5% Triton X-100, 0.5 M NaCl, pH 8 prior to solubilization facilitated by sonication in 100 mM Tris, pH 8, 7 M Guanidine HCl. After centrifugation to pellet insoluble materials and the addition of dithiothreitol, proteins in the supernatant were refolded using a shuffle buffer containing 100 mM Tris, pH 8, 0.5 M L-Arginine, 1 M Urea, 2 mM EDTA, 1 mM oxidized glutathione (fresh made), and 1 mM Reduced glutathione (fresh made) that was dialyzed at 4° C. against 25 mM Tris, pH 8, 0.1 M Urea, and 1 mM EDTA. Following 0.45 μm filtration, desired proteins were purified using ion exchange and size exclusion chromatography. Final protein samples were analyzed by SDS-polyacrylamide gel electrophoresis and stored at −80° C.
This Example describes an exemplary in vivo study to evaluate epithelial trafficking and delivery functions of the exotoxin derived carrier molecules described herein.
The in vivo studies used 7-8 weeks old male adult Wistar rats with an average weight of about 250 g. Where required, experiments were performed using a non-recovery protocol. Generally, rats were anesthetized using inhaled isoflurane and euthanized, when required, by inhaled CO2. Experiments were initiated by making an about 4 cm long abdominal incision to access the mid-jejunum region of the small intestine. Upon making the incision, approximately 50 μL of a prepared solution containing the delivery construct or multiple delivery constructs in a concentration of about 1-1.5 mg/mL was injected into the intestinal lumen of an area devoid of foodstuffs through a 27-gauge needle using a 1 mL syringe. The mesentery adjacent to the site of injection was labeled with a marker and the intestine was returned to the abdominal cavity, with the incision being closed with clamps At specific time points, the injected intestine was retrieved, surgically isolated and flushed with a 4° C. isotonic PBS solution.
Washed, excised samples were fixed (4% paraformaldehyde in PBS) overnight at 4° C. before dehydration through graded series of ethanol/water solutions and overnight incubation in chloroform. Dehydrated tissues were immersed in wax, sectioned, and mounted on polylysine slides and processed for antigen retrieval using sodium citrate. Afterward, sections were permeabilized with 0.2% Triton-X100 in PBS prior to thrice washing in PBS and blocking with 2% BSA+2% serum of the animal the secondary antibodies have been raised. Primary antibodies were diluted in 1% BSA, 0.1% Triton-X100 in PBS and incubate overnight at 4° C. in humidified air. Fluorescent secondary antibodies were diluted in 1% BSA, 0.1% Triton-X100 in PBS and incubated for 2 hours at room temperature prior to processing for confocal microscopy. On occasion, an approximately 1 cm section of intestine at the injection site was collected for biochemical studies.
This Example shows an exemplary list of proteins or markers for specific cell compartments that were analyzed using immunohistochemical (IHC) staining and immuno-fluorescence confocal microscopy and when evaluating the delivery constructs of the present disclosure.
The following TABLE 13 shows exemplary Cell compartment specific protein markers used herein. For example, Cholix derived delivery constructs comprising an IL-10 as the heterologous cargo were followed during experiments using either a monoclonal antibody (mAb) against IL-10 and/or a polyclonal antibody (pAb) raised against the Cholix carrier (e.g., a truncated domain I).
This example describes trans-epithelial transport of delivery constructs comprising truncated Cholix carriers (e.g., truncation in domains II and/or Ib) and truncated PE carriers (e.g., truncation in domain II and/or Ib) conjoined to biologically active cargos across polarized intestinal epithelium occurred (e.g., via apical-to-basolateral transcytosis).
Using the purified isolated monomeric forms of the various delivery constructs prepared as described in EXAMPLE 1, a series of in vivo transport studies were performed using the rat intra-luminal injection model (see additional methods section below). In this analysis, a rat is maintained under isoflurane anesthesia for the duration of this non-recovery study. During this time, the small intestine is exposed following a midline abdominal incision and a mid-jejunum region is selected with the adjacent mesentery being identified using an indelible marking pen. At the location, a 50 μL injection volume was used to administer ˜5 μg of Constructs 7-12. The test protein was dissolved in phosphate buffered saline (PBS) and injected using a 28-gauge needle. After intra-luminal injection, the small intestine segment was returned to the abdominal cavity and retrieved at set periods of time.
Once retrieved, the tissue segment exposed to Constructs 7-12 was flushed with PBS, lightly fixed in paraformaldehyde, and prepared for fluorescence microscopy (see additional methods section below) where the delivery construct was detected using a polyclonal raised against the PE or Cholix that was recognized using a secondary antibody labelled with a red fluorescent dye. The presence or absence of transport for Constructs 7-12 is depicted in
Uptake of each of Constructs 7-12 into a limited population of cells within the Lamina propria was consistent with that observed previously for full-length PE. The finding that efficient trans-epithelial transport of PE across polarized intestinal epithelium occurred even for Construct 12 (PE252-RFP, e.g., amino acid with SEQ ID NO: 137 coupled to amino acid with SEQ ID NO: 220) was surprising and remarkable, suggesting that not only trans-epithelial transport across polarized intestinal epithelial cells, but also targeting to specific cells within the submucosal compartment can be achieved by elements found within domain I (SEQ ID NO: 137) of PE.
Based upon the surprising findings using the PE Constructs 7-12, Construct 6 (Cholix265-RFP), which comprises only domain I of Cholix (SEQ ID NO: 4) was evaluated. Immunofluorescence assessment of Cholix265-RFP (e.g., amino acid of SEQ ID NO: 4 or 5 coupled to SEQ ID NO: 220) transport across rat small intestine in vivo produced a similar outcome as observed with PE Construct 12. Evaluation using an antibody to both the Cholix and the RFP component was used to demonstrate that both elements of the chimera were being transported (see e.g.,
In this example, delivery constructs comprising the amino acid sequences set forth in SEQ ID NO: 146 (Construct 13) and SEQ ID NO: 146 (Construct 14) were prepared, and evaluated as described above in EXAMPLE 2. The chimeric Cholix-PE constructs of this example comprise mixed domains I, II, Ib, and III from either the Cholix exotoxin or the PE exotoxin as described herein.
The chimeric carrier construct 13 (SEQ ID NO: 146) comprises a Cholix domain I derived from the sequence set forth in SEQ ID NO: 1 (amino acid residues 1-265 of SEQ ID NO: 2), a PE translocation domain II derived from the sequence set forth in SEQ ID NO: 138, a PE domain Ib derived from the sequence set forth in SEQ ID NO: 139, and a non-toxic PE catalytic domain III derived from the sequence set forth in SEQ ID NO: 140. The chimeric carrier construct 14 (SEQ ID NO: 147) comprises a PE domain I derived from the sequence set forth in SEQ ID NO: 137, a Cholix carrier translocation domain II derived from the sequence set forth in SEQ ID NO: 126, a Cholix carrier domain Ib derived from the sequence set forth in SEQ ID NO: 127, and a non-toxic Cholix carrier catalytic domain III derived from the sequence set forth in SEQ ID NO: 128.
As shown in
This example demonstrates the transcytosis function of truncated Cholix derived carrier polypeptides, wherein, importantly, the truncation occurred at various locations within the domain I of the Cholix exotoxin.
The non-cleavable polyglycine-serine peptide spacer GGGGSGGGGSGGGGS (SEQ ID NO: 210) was used to couple human growth hormone (HGH) (SEQ ID NO: 214) to the C-terminus of various modified Cholix carrier polypeptides to prepare the following delivery constructs for evaluation according to the protein production procedure described in EXAMPLE 1 above (in this bacterially produced): 1) SEQ ID NO: 160, which comprises a modified Cholix carrier truncated at amino acid residue 187 of SEQ ID NO: 5; 2) SEQ ID NO: 159, which comprises a modified Cholix carrier truncated at amino acid residue 151 of SEQ ID NO: 5; 3) SEQ ID NO: 158, which comprises a modified Cholix carrier truncated at amino acid residue 134 of SEQ ID NO: 5; 4) SEQ ID NO: 161, which comprises a modified Cholix carrier truncated at amino acid residue 206 of SEQ ID NO: 5; 5) SEQ ID NO: 162, which comprises a modified Cholix carrier truncated at amino acid residue 245 of SEQ ID NO: 5; 6) SEQ ID NO: 163, which comprises a modified Cholix carrier truncated at amino acid residue 251 of SEQ ID NO: 5; and 8) SEQ ID NO: 165, which comprises a modified Cholix carrier comprising amino acid residues 40-187 of SEQ ID NO: 5.
In order to analyze the produced fusion proteins, constructs were injected into the lumen of the small intestine of rats and the injection site was collected 5, 10 or 15 minutes after injection. The tissue was fixed and sectioned then stained with anti-Cholix and anti-HGH antibodies. Fluorescent secondary antibodies were used to visualize the protein location using confocal microscopy. As depicted in
This suggests that the N-terminal can be involved in the transport pathway but is not sufficient for complete transcytosis through the cell. The surprising findings depicted in
This example demonstrates apical-to-basolateral transcytosis of a modified, non-toxic Cholix (ntChx) across polarized intestinal epithelial cells in vitro.
In this example, the Cholix construct was rendered non-toxic through an amino acid variation of a specific glutamic acid residue (substituted with alanine) within the enzymatic pocket for ADP-ribosylation, resulting in the E581A substitution and a polypeptide with the amino acid sequence set forth in SEQ ID NO: 3 (ntChx).
transport at 37° C. of non-toxic E581A Cholix (ntChx) was measured across confluent sheets (0.6 cm2 filter surface area) of primary human intestinal epithelium in vitro, with concentrations of 2.5-200 μg/mL being applied to the apical surface and the amount of ntChx in the basal compartment after 2 h being measured by ELISA (
A time-course assessing transcytosis of ntChx at concentrations of 5, 10, and 20 μg/mL demonstrated that ntChx transcytosis began to reach a linearity after an approximately 20-25 min lag phase (
The apical membrane surface pH of the small intestinal epithelium can be between 5 and 7 (17). transcytosis across primary human intestinal epithelium in vitro tested for 20 μg/mL and examined after 120 min was observed to be approximately twice as efficient when the apical media was pH 7 compared to pH 5, while the basal pH of 7 or 5 did not seem to have an effect (
Without being bound to any theory, it was assumed that the greater variability observed for outcomes where the apical pH of 5 was tested on ntChx transport can have been due to efforts by the epithelium to neutralize this apical compartment during the course of the study that can be occurring just at the apical plasma membrane in close proximity to the site of receptor-endocytosis of ntChx. In sum, these data suggest that ntChx as disclosed herein can be capable of efficient, consistent, and continuous transport across human intestinal epithelium through a receptor-mediated process that can not result in significant size modification to the transported protein.
This example demonstrates apical-to-basolateral transcytosis of ntChx (SEQ ID NO: 3) across polarized intestinal epithelial cells in vivo, examining the ability of ntChx to transport across an intestinal epithelium in vivo by direct intra-luminal injection (ILI) into rat jejunum.
Immunofluorescent microscopic images showed that ntChx, identified using an anti-Cholix polyclonal antisera, entered into epithelial cells rapidly and trafficked through these epithelial cells in vesicular-like structures that involved clatherin co-localizations, with the transcytosis process being completed within minutes (
ILI of ntChx into rat jejunum appeared to restrict the exposure to the upper segments and tip of the intestinal villi.
This example demonstrates apical-to-basolateral transcytosis of ntChx (SEQ ID NO: 3) that involves accessing specific vesicular compartments (e.g.,
Transcytosis of ntChx can involve receptor-mediated endocytosis processes and subsequent vesicular trafficking that avoids the typical fate for ligands internalized by this route of lysosomal degradation. A number of obligate and facilitative intracellular pathogens are capable of subverting host cells endocytic and secretory pathways that restrict their exposure to the lysosomal through effector proteins capable or manipulating host cells processes. This example examined ntChx-containing vesicles undergoing transcytosis to determine the identity of associated proteins that can define the trafficking elements and cellular compartments that can be involved in transcytosis of Chx and Chx variants as disclosed herein.
Upon uptake at the apical plasma membrane, ntChx-positive vesicles were observed to co-localize with Ras-related protein Rab 5 and early endosomal antigen 1 (EEA1) (
Apical application of ntChx-NPs resulted in a transcytosis process consistent with that observed for ntChx alone and without co-localization with LAMP1-positive structures (
This example demonstrates the in vivo transport of Cholix domain I (e.g., SEQ ID NO: 4 or SEQ ID NO: 4) truncated carrier proteins as described in EXAMPLE 6 compared to non-toxic full-length Cholix as described in EXAMPLE 7.
Transcytosis of ntChx (SEQ ID NO: 3) in vitro was monitored by Western blot and immunofluorescence microscopy using a polyclonal antibody raised against the full-length protein. To test whether this polyclonal antibody can provide equivalent coverage across all regions of ntChx for the purpose of detecting truncated forms of the exotoxin, the capacity for a truncated form of Cholix to ferry a protein cargo that could be used to assess transcytosis equivalence was investigated.
Genetic chimeras of full-length protein (ntChx) and a version of the protein composed of only domain I were prepared, comprising the amino acid sequence set forth in SEQ NO: 5, and its C-terminus was used to conjugate red fluorescent protein (RFP, SEQ ID NO: 220) via its N-terminus, resulting in the construct having the amino acid sequence set forth in SEQ ID NO: 157). RFP alone, having a molecular weight of 25.9 kDa (225 amino acid residues) was used as a transcytosis control.
The data show that the extent of transcytosis of RFP alone was minimal compared that of ntChx-RFP and Cholix domain I (M+Cholix1-265 or residues 1-266 of SEQ ID NO: 5)—RFP (SEQ ID NO: 156) when examined 30 min after ILI in to rat jejunum in vivo (
This example demonstrates the in vitro apical-basolateral transcytosis and intracellular delivery functions of various truncated Cholix domain I carrier proteins conjugated to human growth hormone via a spacer as described above in EXAMPLE 6.
To further explore the function of elements within Cholix domain I involved in transcytosis, a series of chimeras that contained a pharmaceutically-relevant protein, human growth hormone (HGH, SEQ ID NO: 214), were prepared as genetic constructs. Each truncated sequence of the Cholix domain I (SEQ ID NO: 5, bacterially expressed) was conjugated via the C-terminus to the N-terminus of HGH through a G4SG4SG4S spacer sequence (SEQ ID NO: 210), resulting in the chimeras having the amino acid sequences set forth in SEQ ID NO: 158, SEQ ID NO: 159, SEQ ID NO: 160, SEQ ID NO: 161, SEQ ID NO: 162, SEQ ID NO: 163, and SEQ ID NO: 164. In the case of the K187 truncation of Cholix domain I with SEQ ID NO: 5, the first 39 amino acids were also deleted to produce the E40-K187 fragment of Cholix domain I (SEQ ID NO: 5) to yield the construct with the amino acid sequence set forth in SEQ ID NO: 165 (TABLE 14).
Experiments investigating the transport capabilities of these chimeras across human intestinal epithelial monolayers in vitro demonstrated that the delivery constructs with the amino acid sequences set forth in SEQ ID NO: 158, SEQ ID NO: 159, SEQ ID NO: 160, and SEQ ID NO: 165 did not transport, unlike SEQ ID NO: 161, as shown in
These results suggest that domain I of Cholix is sufficient for apical-to-basal transport, and that it can function as a transcytosis element to deliver various heterologous cargos across epithelial cells, wherein the heterologous cargo may replace the domains II, Ib, and III of the Cholix exotoxin. Additionally, it has been demonstrated that elements within the first 206 amino acid residues of the bacterially expressed Cholix protein (e.g., SEQ ID NO: 5, or, alternatively the first 205 amino acid residues of SEQ ID NO: 4) can be sufficient for the transcytosis function and thus may be used as an efficient carrier for various heterologous cargos. Remarkably, the results suggest that the transcytosis efficiency of these first 206 amino acids of SEQ ID NO: 5 may even be greater than that of the entire domain I (e.g., SEQ ID NO: 5) or the full-length mature Cholix exotoxin (e.g., SEQ ID NO: 1 or SEQ ID NO: 2). Thus, the herein disclosed truncated Cholix domain I constructs can be used to efficiently shuttle heterologous cargo molecules such as therapeutic and/or diagnostic agents across an epithelial cell layer (e.g., the gut epithelium) enabling oral administration of therapeutic and/or diagnostic agents (e.g., larger polypeptides or proteins such as antibodies) that are otherwise administered via parenteral administration routes (e.g., intravenously of subcutaneously). In addition, these results show that truncated versions of Cholix domain I may be used to deliver various heterologous cargo into epithelial cells using the delivery constructs as described herein.
This example demonstrates the in vivo transport of a Cholix domain I (e.g., SEQ ID NO: 4 or SEQ ID NO: 5) truncated protein chimeras across gut epithelial cells for delivery of heterologous cargo (in this example: human growth hormone).
Selected truncation chimeras as shown above in TABLE 14 of EXAMPLE 11 were examined for their capacity for transcytosis in vivo following ILI into rat jejunum. The notation indicating the length and residue at which the truncated occurred of the truncated Cholix domain I carriers are relative to SEQ ID NO: 5.
The data obtained in these studies show that while M+Cholix1-133-(SEQ ID NO: 10)-HGH (SEQ ID NO: 158) did not enter into rat epithelium by 15 min (
These results suggest that elements of Cholix domain I (SEQ ID NO: 5) between E134 and D151 are essential to apical endocytosis, that elements within the first 39 amino acids of Cholix domain I may be critical for trafficking from the apical vesicular pool to the basal vesicular pool, and that elements between K187 and K206 may be critical for Cholix secretion from the basolateral surface of enterocytes. Thus, these results demonstrate that Cholix domain I and truncated version thereof, e.g., those comprising the first 206 amino acid residues of Cholix domain I (SEQ ID NO: 5), can efficiently deliver various cargo across epithelial cells (e.g., across polarized gut epithelial cells of a subject). Moreover, these results show that truncated versions of Cholix domain I may be used to deliver various heterologous cargo into epithelial cells using the delivery constructs as described herein.
This example demonstrates recapitulation of Cholix domain I (SEQ ID NO: 5) transcytosis using functional elements, e.g., functional peptide fragments, of Cholix domain I to generate a synthetic polypeptide that is capable of delivery into epithelial cells and/or across an epithelial cell layer (e.g., an epithelial cell monolayer and/or a gut epithelium of a subject) in vitro (
To that end, transcytosis experiments using specific peptides derived from portions of Cholix domain I (SEQ ID NO: 5) that were identified as critical for apical endocytosis were used to model the various steps and aspects such as intracellular trafficking, and basal membrane secretion of transcytosis of full-length ntChx, exemplary peptide fragments of Cholix domain are shown below in TABLE 15 (including the molecular mass and isoelectric point (pI)).
134ELDQQRNII
1MVEEALNIFD
151DLDNQTLEQ
187KAAQKEGSR
For example, the peptide 134ELDQQRNIIEVPKLYSID151 (SEQ ID NO: 148) was the element that differed between M+Cholix1-150-HGH (amino acid sequence set forth in SEQ ID NO: 159) and M+Cholix1-133-HGH (amino acid sequence set forth in SEQ ID NO: 158), one chimera that could undergo endocytosis and one that could not. Another peptide of interest is within the first 39 amino acids (1MVEEALNIFDECRSPCSLTPEPGKPIQSKLSIPSDVVLD39, SEQ ID NO: 149), which was lacking in the M+Cholix39-186 construct (SEQ ID NO: 165) that lacked the ability to traffic from the apical portion of the epithelial cell to the basal domain following endocytosis. The peptide that provided the difference between M+Cholix1-150-(SEQ ID NO: 210)-HGH and M+Cholix1-186-(SEQ ID NO: 210)-HGH was 151DLDNQTLEQWKTQGNVSFSVTRPEHNIAISWPSVSYK187 (SEQ ID NO: 151); M+Cholix1-150-(SEQ ID NO: 210)-HGH showed the ability to access a supra-nuclear area of the cell that was not accessed by M+Cholix1-150-(SEQ ID NO: 210)-HGH. Finally, M+Cholix1-265-(SEQ ID NO: 210)-HGH was secreted from the basal surface of intestinal epithelial cells while M+Cholix1-186-(SEQ ID NO: 210)-HGH was not; 187KAAQKEGSRHKRWAHWHTGLAL206 (SEQ ID NO: 152) is the peptide that describes the difference in the sequences of these two chimeras (see e.g.,
A polymer framework containing peptide sequences of amino acids from positions 1-39, 134-151, 151-178, and 178-206 of Cholix domain I with SEQ ID NO: 5 in various combinations was labeled with different of quantum dot forms.
The in vitro data show that some selected peptide sequences of Cholix domain I peptide elements are sufficient to achieve apical to basal transcytosis in vitro and in vivo (
The data shows that various Cholix sequence variants as disclosed herein retain efficient endocytosis following uptake from the lumen but lack ability to complete transcytosis, being useful to target apical or apical and basal vesicular structures. From the data presented, it appears that Cholix utilizes a receptor-mediated-type endocytosis process that involves amino acids 134-151, which provides access to an early endosomal vesicular compartment in the apical portion of enterocytes (e.g., gut epithelial cells). Amino acids 151-187 of the Cholix exotoxin domain I (e.g., SEQ ID NO: 5) as described herein appear to allow its movement to a supra-nuclear compartment consistent with a sorting site in the cell for secretory events, and thus allow delivery of various cargos to those locations as well. Movement to the basal compartment of the cells becomes more efficient with the presence of amino acids 1-40. Finally, amino acids 187-206 provide a mechanism for secretion from the basal membrane that releases the entire and intact protein into the Lamina propria where it could provide therapeutically effective concentrations of therapeutic cargo molecules (e.g., interleukins), present antigens to immune cells, and/or allow the cargo to be taken up into systemic circulation for delivery to other target organs/tissues in a subject.
This example demonstrates that Cholix domain I derived delivery constructs utilize distinct compartments for trafficking into and across (e.g., via transcytosis) epithelial cells using various marker proteins (see e.g., EXAMPLE 3) that indicate Cholix derived carrier constructs utilize specific and endogenous trafficking pathways. The study described in this example was conducted using the Cholix derived delivery construct having the amino acid sequence set forth in SEQ ID NO: 154 (comprising the M+Cholix386 carrier coupled to IL-10 via the spacer with the sequence set forth in SEQ ID NO: 210, M=N-term. methionine).
EEA1 antigen.
Rab7. Moreover, it was shown that the Cholix-IL-10 delivery constructs (SEQ ID NO: 154, top right) strongly co-localizes with the Rab7 (top left) predominantly in the apical compartment of enterocytes, but with only limited co-localization in cells within the Lamina propria, suggesting the presence of the Cholix derived delivery constructs in late endosome compartments (
LAMP1. LAMP1 was identified in large, specific vesicles consistent mature lysosomes that were devoid of Cholix-IL-10 delivery constructs (SEQ ID NO: 154, whitearrows). Cholix-IL-10 chimera, however, also co-localizes with the LAMP1 antigen in cellular locations other than lysosome-like structures, consistent with vesicle trafficking at both the apical and basal domains of enterocytes, suggesting the presence of the Cholix derived delivery constructs in lysosomal compartments (
Clathrin. Next, Cholix-IL-10 chimera (SEQ ID NO: 154) also strongly co-localized with clathrin-coated vesicles, particularly in areas adjacent to the nucleus and with Rab 1 predominantly in the basal compartment of enterocytes as well as in selected cells within the Lamina propria (
Calnexin. Cholix-IL-10 chimera (SEQ ID NO: 154) co-localized with the endoplasmic reticulum as demonstrated by calnexin in a pattern adjacent to the nucleus in enterocytes and in a large fraction of cells with in the Lamina propria (
Endoplasmatic reticulum Golgi intermediate compartment. Cholix-IL-10 chimera (SEQ ID NO: 154) strongly co-localizes with the endoplasmatic reticulum Golgi intermediate compartment (ERGIC) and the LAMN1 antigen appeared to re-distribute in response to carrier endocytosis and transcytosis, as shown for 1 (
Giantin. Cholix-IL-10 chimera (SEQ ID NO: 154) did not co-localize with the low levels of giantin present in enterocytes (
58K antigen. The 58K antigen localized in enterocytes at a site apical to the nucleus and the Cholix-IL10 chimera shows some co-localization with this antigen in a manner that suggests a brief movement through this compartment. No 58K antigen was observed in cells within the Lamina propria (
TGN38 antigen. Cholix-IL-10 chimera (SEQ ID NO: 154) showed some level of co-localization with the TGN38 antigen (top right), which showed a cellular distribution that was restricted to the apical side of nuclei in enterocytes and adjacent to the nucleus in a few cells within the Lamina propria (
Rab 1. Cholix-IL-10 chimera (SEQ ID NO: 154, top right) strongly co-localized with Rab 1 (top left) predominantly in the basal compartment of enterocytes and in selected cells within the Lamina propria (
This data demonstrates that the Cholix derived delivery constructs of the present disclosure interact with various endogenous proteins and receptors to harness an endogenous transport system for efficient delivery of cargo across and/or into epithelial cells (e.g., polarized gut epithelial cells).
Based on the results shown above in EXAMPLE 14, this example demonstrates a protocol for the assessment of Cholix interacting receptors and various additional information regarding those interactions. Various Cholix derived delivery constructs including those having an amino sequence set forth in SEQ ID NO: 154 (M+Cholix386-GGGGSGGGGSGGGGS (SEQ ID NO: 210)-IL-10) and a construct comprising the Cholix domain I set forth in SEQ ID NO: 5 coupled to IL-10 (SEQ ID NO: 217) or HGH (SEQ ID NO: 153) via the GGGGSGGGGSGGGGS spacer (SEQ ID NO: 210) were used in this study, e.g., SEQ ID NO: 164. First, a limited set of candidate proteins as carrier protein receptors have been identified through bead capture and mass spectrometry analysis studies. Then, the interactions of the Cholix carrier with these candidate proteins were assessed in vitro (e.g., using Caco-2 cell monolayers) and in vivo (e.g., in the rat jejunum).
Generally, nano-sized magnetic beads (25 nm or 100 nm diameter) were decorated with the non-toxic carrier elements of the Cholix protein using either a biotin-based or poly-histidine-based method of interaction (e.g., using 1D SDS-PAGE, described in e.g.,
After multiple washings, these magnetic bead-enriched vesicles were solubilized in lysis buffer and the protein components present were separated by 2-D SDS-PAGE (
Comparison of outcomes from repeats of this protocol were used to identify a limited set of most promising candidates that were then examined for their content in Caco-2 cells and in rat small intestine (
Microscopic co-localization of candidate proteins and Cholix derived delivery construct was evaluated in rat jejunum in vivo. Here, co-localization of a delivery construct comprising a Cholix carrier protein coupled to IL-10 (SEQ ID NO: 154, M+Cholix386-GGGGSGGGGSGGGGS (SEQ ID NO: 210)-IL-10) with CK8 was shown in vivo, after rat jejunum was treated with a luminal application of the construct having the amino acid sequence set forth in SEQ ID NO: 154 for 1 minute (
To ensure that the receptor distribution was consistent between rat in vivo studies and human intestine, information was compared to IHC studies described in the human atlas. Here, two of the receptors identified by mass spectrometry and verified in rat jejunum were examined.
Knock-down in Caco-2 cells using sh-RNA technology were used to establish stable cell lines that were used to validate the involvement of these target proteins in the apical-to-basal transcytosis of the Cholix carrier protein. These studies were then repeated using rat jejunum in vivo to compare to the Caco-2 cell in vitro findings.
Here, transport of Cholix domain I derived delivery construct in CRISPR knockout HSPC stable Caco-2 cells was evaluated.
Similar studies were conducted for the additional candidate proteins K8 (
Rat jejunum ILI studies demonstrated that GRP75 was distributed in enterocytes in distinct apical and basal vesicular populations; SEQ ID NO: 164 co-localized with GRP75 in vesicles within the apical third of enterocytes not immediately adjacent to the apical plasma membrane (
This data demonstrates that, indeed, Cholix derived carrier and cargo transport and delivery is an active and selective process involving distinct receptors. This may be useful for the targeted delivery and therapeutic and/or diagnostic molecules across and/or to the interior of epithelial cells (e.g., gut epithelial cells) for the treatment and diagnosis of diseases as described herein.
This example demonstrates the assessment of the pH-dependence of a Cholix derived carrier protein (e.g., SEQ ID NO: 4) and one of its interacting receptors during active transcytosis, GRP75.
For this study, Biacore binding interactions were used to examine the pH-dependency of Cholix carrier-GRP75 interactions. Cholix carrier proteins were attached to magnetic beads using the biotin-streptavidin bioconjugation and incubated with purified GRP75 protein in buffer solutions with pH 5.5, 6.5, and 7.5, respectively (
Binding affinities at those three pH levels were generally in the low nanomolar range, however, a significantly higher (approximately 20-fold higher) binding affinity of the Cholix carrier to GRP75 was measured at pH 6.5, indicating pH dependency of this interaction.
In this example, the type of proteins and their compartmental locations in epithelial cells was examined using a Cholix domain I derived delivery construct (SEQ ID NO: 5) that was shown to possess equal, if not higher, transcytosis function than full-length Cholix exotoxin (SEQ ID NO: 1). All amino acid residues and their positions are shown relative to the bacterially expressed Cholix domain I sequence set forth in SEQ ID NO: 5.
Interaction partners for Cholix domain I ending at K266 of SEQ ID NO: 5, bacterially expressed Cholix carrier comprise an N-terminal methionine) were captured using a magnetic bead and isolation procedure followed separated by 2-D gel electrophoresis separation and identified using mass spectrometry as described above in EXAMPLE 15. Importantly, in this example a number of truncated forms of the full-length Cholix exotoxin were also prepared to examine various aspects of these interactions: truncations at amino acid E134, D151, K187, L206, K245, or Q251, or L206 conjoined to the N-terminus of human growth hormone (HGH) through a G4SG4SG4S sequence with this glycine-serine spacer being identified previously for constructing genetic chimeras. In the case of the K187 truncation, we also deleted the first 39 amino acids to produce the E40-K187 fragment of Chx domain I with SEQ ID NO: 5. As described above, e.g., in EXAMPLE 10, the construct with SEQ ID NO: 158 failed to achieve apical entry into intestinal epithelial cells, the construct with SEQ ID NO: 159 and SEQ ID NO: 160 underwent endocytosis to reach both apical and basal vesicular pools within enterocytes but did not to access the Lamina propria, and the construct with SEQ ID NO: 165 underwent endocytosis but failed to migrate from the apical to the basal vesicular compartment of the enterocyte, and, finally, the construct with SEQ ID NO: 164 efficiently and rapidly completes transcytosis. Thus, the first 206 amino acids of Cholix domain I were evaluated for elements that may participate in the events that resulted in apical-to-basal transcytosis.
First, the transmembrane protein 123A (TMEM132A) was evaluated. TMEM132A is a single-pass transmembrane protein that contains cohesin and three tandem immunoglobulin domains, thus connecting the extracellular medium with the intracellular cytoskeleton. Interactions between TMEM132A and serine/threonine-protein phosphatase 1 (PP1) have been demonstrated, providing a mechanism to regulate intracellular cytoskeletal events through a RVxF interaction motif.
It was found that Cholix domain I (SEQ ID NO: 5, bacterially expressed) enriched the isolation of TMEM132A along with catalytic and regulatory subunits of the PP1 complex. ELISA-based studies showed that Cholix domain I with SEQ ID NO: 5 interacted with the extracellular domain of TMEM132A; SPR studies showed this interaction to occur at pH 7.5 and less at pH 5.5. Knock-down studies in Caco-2 cells, to generate Caco-2TMEM132A− cells, showed that reduction of TMEM132A dramatically reduced the transport of transcytosis of Cholix domain I with SEQ ID NO: 5.
Intraluminal injection (ILI) studies performed in rat jejunum resulted in co-localization of the Cholix domain I-HGH delivery construct (SEQ ID NO: 164) with TMEM132A that was restricted to the apical plasma membrane of enterocytes. A time course examining transcytosis of SEQ ID NO: 164 suggested that TMEM132A remained at or adjacent to the apical plasma membrane and did not redistribute significantly to other regions of these polarized epithelial cells. While the construct with SEQ ID NO: 158 did not significantly enter into enterocytes following apical application, the construct with SEQ ID NO: 159 did enter, suggesting that a domain of Chx critical for apical cell entry resided with the 17 amino acids that discriminated where two carrier constructs. Once internalized, the internal pH of an early or a recycling endosome can drop from neutrality to ˜6.0. Examination of interactions between the construct having sequence set forth in SEQ ID NO: 164 and TMEM132A demonstrated that these occurred to a much greater extent at pH 7.4 compared to pH 5.5, consistent with the theory that release from an internalization receptor, in this case TMEM132A, could be facilitated by decreased vesicle pH that could occur following apical Chx uptake.
Studies examining clathrin distribution in rat enterocytes did not show co-localizations with the construct having sequence set forth in SEQ ID NO: 164 at the apical surface, suggesting that Chx entry may not involve clathrin-mediated uptake. Strikingly, the cellular distribution of TMEM132A following the construct having sequence set forth in SEQ ID NO: 164 application remained at the apical surface, but was found more frequently in apical vesicles following apportion of the construct with SEQ ID NO: 159, suggesting that the lack of other elements within Cholix domain I (SEQ ID NO: 5) were necessary for the handoff to a receptor (or receptors) required for the next step in its trafficking. These results suggest that Chx can engage TMEM132A at the luminal surface and that these interactions are involved in the initial endocytosis process from the intestinal lumen and that subsequent interactions within early endosomes are required for the transcytosis process to continue.
Cytokeratin 8 (CK-8) was one of several proteins in this family identified in the initial screen as a potential Chx interaction partner; CK-8 was previously identified as a cell-surface receptor for the Pet toxin secreted from enteroaggregative E. coli. ELISA-based binding studies showed CK-8 to interact with TMEM132A and also Chx. CK-8 distribution in rat enterocytes was restricted to the apical surface and at discrete domains in the apical and basal compartments. A time course examining transcytosis of the construct having sequence set forth in SEQ ID NO: 164 suggested that CK-8 cellular distribution did not change dramatically following apical M+Cholix1-265-HGH (SEQ ID NO: 164) application and that some co-localizations were observed in the apical compartment of enterocytes. Knock-down of CK-8 was performed in Caco-2 cells (Caco-2CK8−) and evaluated with its impact on transcytosis of the construct having sequence set forth in SEQ ID NO: 164. CK-8 knockdown, as further shown above in EXAMPLE 15, did not affect the transport of the construct having sequence set forth in SEQ ID NO: 164, demonstrating the ability for this in vitro model to determine selective function for interaction partners in the transcytosis process of Chx. These studies point out that proteins identified in Chx pull-downs that co-localize with cellular compartments visited by the construct having sequence set forth in SEQ ID NO: 164 may not be essential for transcytosis.
This example demonstrates that distinct proteins such as GRP75 are involved in early endosomal sorting of Cholix and Cholix derived delivery constructs (e.g., those having an amino acid sequence set forth in SEQ ID NO: 158-SEQ ID NO: 165).
Transcytosis of the delivery construct was demonstrated to consistently traffic in large quantities across enterocytes. Specific compartments that strongly co-localized with this transcytosis included early endosomes and late endosomes. The Cholix derived carrier appeared to be associated with clathrin-coated vesicles in the vicinity of the ER-Golgi network organized adjacent to enterocyte nuclei. Co-localization of the Cholix derived carrier was observed with the ER and ERGIC, also described as LMAN1 (lectin, mannose binding 1), but limited in its association with elements of the cis-Golgi, Golgi, and trans-Golgi network. The Cholix derived carrier having SEQ ID NO: 164 co-localized with recycling endosomes near the basal surface of enterocytes in a manner that might coordinate with ERGIC re-distribution. ERGIC-53 can also function as an intracellular cargo receptor involved in the anterograde transport of a limited number of glycoprotein ligands in the early exocytic pathway and is used by a number of RNA viruses as part of their exocytosis strategy. ELISA-based binding studies demonstrated that the construct having sequence set forth in SEQ ID NO: 164 can associate with ERGIC-53 at pH 7.4, but this interaction is significantly stronger at pH 5.5. SPR studies further supported this pH-dependent interaction.
The observed distribution of GPR75 in both apical and basal vesicular compartments of enterocytes did not suggest a role for an efficient vectored routing mechanism of the construct having sequence set forth in SEQ ID NO: 164 from an apical to a basal vesicular compartment; rather, GPR75 could play a role in the local vesicular pools in each location. Further, we did not observe any subverted distribution of GPR75 as has been observed for the actions of other bacterial effector proteins. Thus, we conjectured that Chx interactions with GPR75 may provide some function other that routing vesicles from an apical endosomal compartment to a basal endosome compartment and hypothesized that GPR75 interactions could function to minimize routing of this bacterial effector protein from vesicles to lysosomes at both locations.
Additional studies with TMEM132A demonstrated a greater interaction affinity with the construct having sequence set forth in SEQ ID NO: 164 at neutral compared to an acidic pH suggesting that once internalized, the construct having sequence set forth in SEQ ID NO: 164 could find another receptor for trafficking while the internalization receptor cycled back to the apical surface of the cell. In this hypothesis, the trafficking receptor would have a greater interaction affinity for Chx at an acidic pH relative to neutrality. Indeed, examination of GPR75 interactions with the construct having sequence set forth in SEQ ID NO: 164 demonstrated a higher affinity between these two molecules at pH 5.5 compared to pH 7.4.
This data demonstrates that the herein described Cholix derived delivery constructs efficiently access the enterocytes (e.g., polarized gut epithelial cells) and interact with proteins involved in early endosomal sorting, allowing these constructs to avoid intracellular degradation pathways that results in the delivery and transport of intact carrier and cargo, e.g., across epithelial cell via transcytosis and/or to the interior via endocytosis.
This example demonstrates that Cholix domain I derived delivery constructs interact with distinct proteins such as ERGIC-53 during intracellular sorting.
Luminal introduction of the delivery constructs with SEQ ID NO: 164 in the rat ILI model provided data to support ERGIC-53 as an element subverted by Cholix constructs of the present disclosure to achieve efficient transcytosis. Prior to and at times immediately following apical application of the construct having sequence set forth in SEQ ID NO: 164, ERGIC-53 was observed in discrete populations in enterocytes that was focused near the apical surface of the cell nucleus, a location where ERGIC is consistently located. Within a few minutes of luminal application of the construct having sequence set forth in SEQ ID NO: 164, ERGIC-53 was observed to move to areas within enterocytes adjacent to the apical plasma membrane and to a basal domain. Thus, Cholix carrier transcytosis and ERGIC-53 redistribution to the basal area of enterocytes was coincident.
Since ERGIC-53 is involved in glycoprotein export from the ER, the cellular distribution of an ER resident protein ribophorin 1 (dolichyl-diphosphooligosaccharide protein glycosyltransferase subunit 1) that mediates N-glycosylation events was examined. Importantly, ribophorin 1 was observed in a pull-down using GRP75. Transcytosis of the construct having sequence set forth in SEQ ID NO: 164 was observed following its ILI into rat jejunum did not affect the intracellular distribution of ribophorin 1, showing it to co-localize to a limited extent in the apical vesicular compartment where ribophorin 1 was present throughout the time course during which ERGIC-53 was subverted to the basal compartment. Additionally, ERGIC-53 interacts with a constellation of proteins, including SEC24, in its role as a soluble cargo receptor. Notably, a pull-down with GRP75 as bait identified SEC24. Similarly, apical application of the construct having sequence set forth in SEQ ID NO: 164 did not induce a gross alteration of intracellular compartment organization.
The ERGIC is involved in sorting soluble molecules destined for secretion from the cell and ERGIC-53 undergoes a process of concentrative sorting that involves the coat protein COPII. Since both COPI and COPII are involved in vesicle trafficking at the ER-Golgi interface, the potential for these coat proteins to co-localized with the construct having sequence set forth in SEQ ID NO: 164 during the transcytosis process was investigated. Rat enterocytes demonstrated a COPI distribution beneath the apical plasma membrane and at a supra-nuclear site consistent with the Golgi apparatus, a distribution that was also observed following the apical application of the construct with SEQ ID NO: 158 that did not enter these cells, and the construct with SEQ ID NO: 165 that underwent endocytosis but remained in an apical vesicular compartment. Similar to that observed for untreated tissues or those exposed to the construct with SEQ ID NO: 158, ERGIC-53 (LMAN1) distribution in enterocytes exposed to an apical application of the construct with SEQ ID NO: 159 or the construct with SEQ ID NO: 165 remained primarily in an apical vesicular compartment, with very little basal vesicular compartment distribution in enterocytes (
Apical application of the construct with SEQ ID NO: 159 or the construct with SEQ ID NO: 165 resulted in the co-localization of HGH with COPI beneath the apical membrane and at a supra-nuclear site, with limited co-localization events being observed in the apical vesicular pool region of enterocytes. Apical treatment with the construct with SEQ ID NO: 160 resulted in extensive co-localization of HGH with COPI beneath the apical membrane and some co-localizations within the apical vesicular compartment, and less co-localization events in the supra-nuclear region.
This data demonstrate that Cholix derived delivery constructs such as those having amino acid sequences set forth in SEQ ID NO: 158, SEQ ID NO: 159 and SEQ ID NO: 165 can be used to delivery various cargo molecules to intracellular compartments of an epithelial cell. This may be particularly useful for the targeted delivery of therapeutic and/or biologically active molecules capable of eliciting a therapeutic and/or biological effect at those locations.
This example demonstrates a mechanism that can be harnessed to achieve efficient basal release of Cholix derived delivery constructs, allowing efficient transport of cargo across epithelial layers (e.g., a gut epithelium).
The basement membrane-specific heparan sulfate proteoglycan protein (HSPG, HSPG2 or perlecan), an integral component of basement membranes that support the simple columnar epithelium of the intestine, was identified in initial capture studies (see e.g.,
Stable knock-down of perlecan in Caco-2 cells (Caco-2HSPG2−) grown in a polarized format significantly reduced the ability of the construct with SEQ ID NO: 164 to complete transcytosis in vitro. ELISA-based binding studies demonstrated that Chx can associate with perlecan. SPR studies showed that Chx interacts with perlecan at pH 5.5 but not at pH 7.4.
In enterocytes from untreated animals of following apical exposure with the construct with SEQ ID NO: 158, perlecan-positive immunolabeling was observed in vesicles that were distributed in the apical, supra-nuclear, and basal compartments; ERGIC-53 (LAMN1) distribution was restricted to a location between the apical and supra-nuclear compartments (
Notably, the Chx transcytosis pathway described herein suggests that Cholix derived carrier proteins coupled to a heterologous (non-Cholix derived) cargo do not result in cellular disorganization, outside of the subversion of ERGIC-53 (LAMN1), indicating that the cargo (e.g., therapeutic) delivery mechanisms described herein do not impair the epithelial layer or the cell itself. Thus, highly efficient cargo delivery without impairing the epithelium of the delivery construct itself may be an important feature of the herein described delivery constructs and methods. It may allow delivery of various therapeutic and/or diagnostic or other cargo molecules in a non-invasive manner, potentially allowing for standards of safety and therapeutic efficacy.
This data demonstrates that specific proteins (e.g., ERGIC-53, ribophilin 1, SEC24, CK-8, TMEM132A, GPR75, and perlecan) are involved in trafficking a Cholix domain I derived delivery construct across an epithelial cell and allow its release from the basal membrane. The identity of the distinct interaction partners and pH-dependencies of these interactions may be particularly useful for the therapeutic applications as the herein described trafficking pathway allows the delivery of Cholix domain I derived carriers coupled to various cargo molecules to reach the basolateral compartment (e.g., Lamina propria) by using endogenous trafficking pathways. However, and demonstrated in EXAMPLE 11 above, specific functional elements of Cholix (and PE) domain I allow the delivery of heterologous cargo to distinct locations within and/or across the epithelium.
Thus, the herein described multi-receptor, multi-compartment pathways used by Cholix derived delivery constructs to efficiently achieve the transcytosis can provide a potential roadmap for the oral delivery of therapeutic molecules (e.g., protein therapeutics such as therapeutic antibodies) that can be coupled to a Cholix domain I carrier or a carrier derived therefrom.
This example shows that portions of the functional sequence elements of Cholix domain I that are described herein to promote transcytosis and apical-to-basal trafficking are located at the protein surface of domain I of the Cholix exotoxin.
Protein structure analyses demonstrated that functional elements required for apical endocytosis, apical-to-basal trafficking and basal release are in proximity to each other on the surface of the Cholix domain I protein.
A surface model of bacterially expressed Cholix domain I (SEQ ID NO: 5) was used to highlight selected areas of potential interest in this transcytosis process due to their projection from the protein surface (
This data shows that portions of the amino acid sequence of Cholix domain I that are distant from each other in terms of amino acid position within the sequence can, in fact, be in close proximity to each other in a 3D configuration of the Cholix domain I protein. This data suggests that the 3D structure and surface morphology of Cholix domain I allows interaction with receptors and receptor elements required to efficient endocytosis and/or transport the epithelial cell. This can be useful to design orally administrable therapeutics comprising such Cholix domain I derived carrier molecules to provide therapeutically effective doses basolateral compartments, the Lamina propria, etc. to elicit therapeutic effects.
All of the articles and methods disclosed and claimed herein can be made and executed without undue experimentation in light of the present disclosure. While the articles and methods of this disclosure have been described in terms of embodiments, it will be apparent to those of skill in the art that variations can be applied to the articles and methods without departing from the spirit and scope of the disclosure. All such variations and equivalents apparent to those skilled in the art, whether now existing or later developed, are deemed to be within the spirit and scope of the disclosure as defined by the appended claims. All patents, patent applications, and publications mentioned in the specification are indicative of the levels of those of ordinary skill in the art to which the disclosure pertains. All patents, patent applications, and publications are herein incorporated by reference in their entirety for all purposes and to the same extent as if each individual publication was specifically and individually indicated to be incorporated by reference in its entirety for any and all purposes. The disclosure illustratively described herein suitably can be practiced in the absence of any element(s) not specifically disclosed herein. The terms and expressions which have been employed are used as terms of description and not of limitation, and there is no intention that in the use of such terms and expressions of excluding any equivalents of the features shown and described or portions thereof, but it is recognized that various modifications are possible within the scope of the disclosure claimed. Thus, it should be understood that although the present disclosure has been specifically disclosed by embodiments and optional features, modification and variation of the concepts herein disclosed can be resorted to by those skilled in the art, and that such modifications and variations are considered to be within the scope of this disclosure as defined by the appended claims.
SEQ ID NO: 1 is a 634 amino acid sequence of mature Vibrio cholera Cholix toxin.
SEQ ID NO: 2 is a 634 amino acid sequence of mature Vibrio cholera Cholix toxin.
SEQ ID NO: 3 is a non-toxic (nt) variant of the mature V. cholera Cholix toxin.
SEQ ID NO: 4 is a domain I of a Cholix toxin.
SEQ ID NO: 5 is a domain I of a Cholix toxin comprising an N-terminal methionine residue (e.g., due to bacterial expression).
SEQ ID NO: 6-SEQ ID NO: 125 are truncated versions of Cholix domain I.
SEQ ID NO: 126 is an amino acid sequence of the V. cholera Cholix carrier translocation domain (domain II).
SEQ ID NO: 127 is an amino acid sequence of the V. cholera Cholix carrier domain Ib.
SEQ ID NO: 128 is an amino acid sequence of the V. cholera Cholix carrier catalytic domain (domain III).
SEQ ID NO: 129 is the amino acid sequence of Cholix1-425.
SEQ ID NO: 130 is the amino acid sequence of Cholix1-415.
SEQ ID NO: 131 is the amino acid sequence of Cholix1-397.
SEQ ID NO: 132 is the amino acid sequence of Cholix1-386.
SEQ ID NO: 133 is the amino acid sequence of Cholix1-291.
SEQ ID NO: 134 is a nucleic acid sequence encoding the mature Vibrio cholera Cholix toxin set forth in SEQ ID NO: 2.
SEQ ID NO: 135 is a nucleic acid sequence encoding the 613 amino acid sequence of mature Pseudomonas exotoxin A (PE).
SEQ ID NO: 136 is a nucleic acid sequence encoding the mature Pseudomonas exotoxin A (PE) set forth in SEQ ID NO: 135.
SEQ ID NO: 137 is an amino acid sequence of the Pseudomonas exotoxin A (PE) receptor binding domain (Domain I).
SEQ ID NO: 138 is an amino acid sequence of the Pseudomonas exotoxin A (PE) translocation domain (Domain II).
SEQ ID NO: 139 is an amino acid sequence of the Pseudomonas exotoxin A (PE) Domain Ib.
SEQ ID NO: 140 is an amino acid sequence of the Pseudomonas exotoxin A (PE) catalytic domain (Domain III).
SEQ ID NO: 141 is the amino acid sequence of PE1-404.
SEQ ID NO: 142 is the amino acid sequence of PE1-395.
SEQ ID NO: 143 is the amino acid sequence of PE1-375.
SEQ ID NO: 144 is the amino acid sequence of PE1-364.
SEQ ID NO: 145 is the amino acid sequence of PE1-277.
SEQ ID NO: 146 is the amino acid sequence of a hybrid delivery construct.
SEQ ID NO: 147 is the amino acid sequence of a hybrid delivery construct.
SEQ ID NO: 148 is the amino acid sequence of a functional peptide sequence derived from Cholix domain I (e.g., for endocytosis).
SEQ ID NO: 149 is the amino acid sequence of a functional peptide sequence derived from Cholix domain I (e.g., for apical-to-basal transport).
SEQ ID NO: 150 is the amino acid sequence of a functional peptide sequence derived from Cholix domain I (e.g., for apical-to-basal transport).
SEQ ID NO: 151 is the amino acid sequence of a functional peptide sequence derived from Cholix domain I (e.g., for supranuclear localization).
SEQ ID NO: 152 is the amino acid sequence of a functional peptide sequence derived from Cholix domain I (e.g., for basal release).
SEQ ID NO: 153 is the amino acid sequence of a Cholix derived delivery construct comprising human growth hormone (HGH).
SEQ ID NO: 154 is the amino acid sequence of a Cholix derived delivery construct comprising interleukin-10 (IL-10).
SEQ ID NO: 155 is the amino acid sequence of a Cholix derived delivery construct comprising interleukin-10 (IL-22).
SEQ ID NO: 156 is the amino acid sequence of a Cholix derived delivery construct comprising red fluorescent protein (RFP).
SEQ ID NO: 157 is the amino acid sequence of a Cholix derived (comprising non-toxic mature Cholix) delivery construct comprising red fluorescent protein (RFP).
SEQ ID NO: 158 is the amino acid sequence of a truncated Cholix domain I delivery construct comprising HGH.
SEQ ID NO: 159 is the amino acid sequence of a truncated Cholix domain I delivery construct comprising HGH.
SEQ ID NO: 160 is the amino acid sequence of a truncated Cholix domain I delivery construct comprising HGH.
SEQ ID NO: 161 is the amino acid sequence of a truncated Cholix domain I delivery construct comprising HGH.
SEQ ID NO: 162 is the amino acid sequence of a truncated Cholix domain I delivery construct comprising HGH.
SEQ ID NO: 163 is the amino acid sequence of a truncated Cholix domain I delivery construct comprising HGH.
SEQ ID NO: 164 is the amino acid sequence of a Cholix domain I delivery construct comprising HGH.
SEQ ID NO: 165 is the amino acid sequence of a truncated Cholix domain I delivery construct comprising HGH.
SEQ ID NO: 166-SEQ ID NO: 186 are the amino acid sequences of various peptidase cleavage sites.
SEQ ID NO: 187-SEQ ID NO: 193 are the amino acid sequences of various GM-1 receptor binding peptides.
SEQ ID NO: 194-SEQ ID NO: 206 are the amino acid sequences of various cleavable spacers.
SEQ ID NO: 207-SEQ ID NO: 213 are the amino acid sequences of various non-cleavable spacers.
SEQ ID NO: 214 is the amino acid sequence of a human growth hormone (HGH).
SEQ ID NO: 215 is the amino acid sequence of a GLP-1 agonist peptide.
SEQ ID NO: 216 is the amino acid sequence of an insulin peptide.
SEQ ID NO: 217 is the amino acid sequence of a human interleukin-10 (IL-10).
SEQ ID NO: 218 is the amino acid sequence of a human interleukin-22 (IL-22).
SEQ ID NO: 219 is the amino acid sequence of an ExtB polypeptide.
SEQ ID NO: 220 is the amino acid sequence of a Red Fluorescent Protein (RFP).
SEQ ID NO: 221 is the amino acid sequence of a Cholix domain I derived carrier coupled to a spacer.
This application is a continuation of PCT/US2019/021474, filed Mar. 8, 2019, which claims the benefit of U.S. Provisional Application Nos. 62/640,168 filed Mar. 8, 2018; 62/640,188 filed Mar. 8, 2018; 62/640,194 filed Mar. 8, 2018, and 62/756,889, filed Nov. 7, 2018 which applications are incorporated herein by reference in their entirety for all purposes.
| Number | Name | Date | Kind |
|---|---|---|---|
| 5328984 | Pastan et al. | Jul 1994 | A |
| 5512658 | Pastan et al. | Apr 1996 | A |
| 5589384 | Lipscombe et al. | Dec 1996 | A |
| 5602095 | Pastan et al. | Feb 1997 | A |
| 5668255 | Murphy | Sep 1997 | A |
| 5696237 | Fitzgerald et al. | Dec 1997 | A |
| 5807832 | Russell-Jones et al. | Sep 1998 | A |
| 5817633 | Heerze et al. | Oct 1998 | A |
| 5863745 | Fitzgerald et al. | Jan 1999 | A |
| 5965406 | Murphy | Oct 1999 | A |
| 6022950 | Murphy | Feb 2000 | A |
| 6051405 | Fitzgerald et al. | Apr 2000 | A |
| 6086900 | Draper | Jul 2000 | A |
| 6086918 | Stern et al. | Jul 2000 | A |
| 6251392 | Hein et al. | Jun 2001 | B1 |
| 6565856 | Skeiky et al. | May 2003 | B1 |
| 6673574 | Stern et al. | Jan 2004 | B2 |
| 6838553 | Hwang et al. | Jan 2005 | B1 |
| 7193055 | Daugherty et al. | Mar 2007 | B2 |
| 7314625 | Fitzgerald | Jan 2008 | B2 |
| 7314632 | Fitzgerald | Jan 2008 | B1 |
| 7335361 | Liao et al. | Feb 2008 | B2 |
| 7378100 | Chang et al. | May 2008 | B2 |
| 7465455 | Chang et al. | Dec 2008 | B2 |
| 7595054 | Liao et al. | Sep 2009 | B2 |
| 7611714 | Mrsny | Nov 2009 | B2 |
| 7618635 | Chang et al. | Nov 2009 | B2 |
| 7666991 | Mrsny | Feb 2010 | B2 |
| 7713737 | Mrsny | May 2010 | B2 |
| 7727538 | Quinn et al. | Jun 2010 | B2 |
| 7824695 | Fitzgerald et al. | Nov 2010 | B1 |
| 7964200 | Mrsny et al. | Jun 2011 | B2 |
| 8092806 | Wallach et al. | Jan 2012 | B2 |
| 8092809 | Fitzgerald | Jan 2012 | B2 |
| 8206950 | Liao et al. | Jun 2012 | B2 |
| 8309102 | Mrsny et al. | Nov 2012 | B2 |
| 8372407 | Liao et al. | Feb 2013 | B2 |
| 8790897 | Quinn et al. | Jul 2014 | B2 |
| 9090691 | Mrsny et al. | Jul 2015 | B2 |
| 9259456 | Kidron | Feb 2016 | B2 |
| 9481714 | Wu et al. | Nov 2016 | B2 |
| 9657063 | Kuo et al. | May 2017 | B2 |
| 10010602 | Chien et al. | Jul 2018 | B2 |
| 10130688 | Mrsny et al. | Nov 2018 | B2 |
| 10400013 | Liao et al. | Sep 2019 | B2 |
| 10617741 | Mrsny et al. | Apr 2020 | B2 |
| 10617767 | Mrsny et al. | Apr 2020 | B2 |
| 10624955 | Mrsny et al. | Apr 2020 | B2 |
| 10624956 | Mrsny et al. | Apr 2020 | B2 |
| 10624957 | Mrsny et al. | Apr 2020 | B2 |
| 10786555 | Mrsny et al. | Sep 2020 | B2 |
| 10786556 | Mrsny et al. | Sep 2020 | B2 |
| 10799565 | Mrsny et al. | Oct 2020 | B2 |
| 11027020 | Mrsny et al. | Jun 2021 | B2 |
| 11246915 | Mrsny et al. | Feb 2022 | B2 |
| 11324833 | Mrsny et al. | May 2022 | B2 |
| 20030054012 | Fitzgerald et al. | Mar 2003 | A1 |
| 20040071736 | Quinn et al. | Apr 2004 | A1 |
| 20050079171 | Fitzgerald et al. | Apr 2005 | A1 |
| 20070003578 | Fitzgerald | Jan 2007 | A1 |
| 20070148131 | Mrsny | Jun 2007 | A1 |
| 20080085277 | Cho et al. | Apr 2008 | A1 |
| 20080317761 | Cines et al. | Dec 2008 | A1 |
| 20090081235 | Fitzgerald et al. | Mar 2009 | A1 |
| 20090092660 | Mrsny | Apr 2009 | A1 |
| 20090142341 | Pastan et al. | Jun 2009 | A1 |
| 20090148401 | Mrsny | Jun 2009 | A1 |
| 20090155297 | Mrsny | Jun 2009 | A1 |
| 20090285771 | Mrsny | Nov 2009 | A1 |
| 20090285848 | Mrsny | Nov 2009 | A1 |
| 20090304684 | Mrsny | Dec 2009 | A1 |
| 20090305978 | Zane | Dec 2009 | A1 |
| 20100151005 | Muro-Galindo et al. | Jun 2010 | A1 |
| 20110250199 | Fitzgerald et al. | Oct 2011 | A1 |
| 20120258104 | Echeverri et al. | Oct 2012 | A1 |
| 20140065172 | Echeverri et al. | Mar 2014 | A1 |
| 20150265718 | Mrsny et al. | Sep 2015 | A1 |
| 20150265719 | Mrsny et al. | Sep 2015 | A1 |
| 20160222362 | Zhang et al. | Aug 2016 | A1 |
| 20180353610 | Mrsny et al. | Dec 2018 | A1 |
| 20200140511 | Porat et al. | May 2020 | A1 |
| 20200354411 | Bard et al. | Nov 2020 | A1 |
| 20210100887 | Chen et al. | Apr 2021 | A1 |
| 20210154304 | Maclean et al. | May 2021 | A1 |
| 20220112259 | Maclean et al. | Apr 2022 | A1 |
| Number | Date | Country |
|---|---|---|
| 0532090 | Mar 1993 | EP |
| 1522585 | Apr 2005 | EP |
| 1000163 | Oct 2005 | EP |
| 1000162 | Sep 2006 | EP |
| 1749833 | Feb 2007 | EP |
| 1379550 | Mar 2009 | EP |
| 1242122 | Sep 2009 | EP |
| 1379273 | Sep 2009 | EP |
| 1757615 | Aug 2011 | EP |
| 1882478 | Mar 2012 | EP |
| 1871880 | Aug 2012 | EP |
| 2065392 | Aug 2012 | EP |
| 2237794 | Apr 2013 | EP |
| 3402810 | Nov 2018 | EP |
| 3302543 | Apr 2020 | EP |
| WO-2006044205 | Apr 2006 | WO |
| WO-2007109110 | Sep 2007 | WO |
| WO-2008021234 | Feb 2008 | WO |
| WO-2009014650 | Jan 2009 | WO |
| WO-2009026328 | Feb 2009 | WO |
| WO-2009115531 | Sep 2009 | WO |
| WO-2009149281 | Dec 2009 | WO |
| WO-2010046783 | Apr 2010 | WO |
| WO-2012036746 | Mar 2012 | WO |
| WO-2012110596 | Aug 2012 | WO |
| WO-2013003824 | Jan 2013 | WO |
| WO-2015113005 | Jul 2015 | WO |
| WO-2015171965 | Nov 2015 | WO |
| WO-2015171965 | Mar 2016 | WO |
| WO-2018067401 | Apr 2018 | WO |
| WO-2018106895 | Jun 2018 | WO |
| WO-2019036382 | Feb 2019 | WO |
| WO-2019133647 | Jul 2019 | WO |
| WO-2019173787 | Sep 2019 | WO |
| WO-2020096695 | May 2020 | WO |
| Entry |
|---|
| Groneberg, D.A., et al. 2003 Respiratory Medicine 97(4): 382-387. (Year: 2003). |
| CA2,948,346 Office Action dated Jun. 2, 2021. |
| Challa et al. Bacterial Toxin Fusion Proteins Elicit Mucosal Immunity against a Foot-and-Mouth Disease Virus Antigen When Administered Intranasally to Guinea Pigs. Adv Virol, vol. 2011, Article ID 713769 (2011). 11 pages. |
| Challa et al. MARTs and MARylation in the Cytosol: Biological Functions, Mechanisms of Action, and Therapeutic Potential. Cells 10:313 (Feb. 3, 2021). 21 pages. |
| Challa et al. Non-toxic Pseudomonas aeruginosa exotoxin A expressing the FMDV VP1 G-H loop for mucosal vaccination of swine against foot and mouth disease virus. Vaccine 25 (2007) 3328-3337. Available online Jan. 12, 2007. |
| CN201580036678.8 Office Action dated Jul. 28, 2021 (w/ English translation). |
| EP19717013.7 Office Action dated May 20, 2021. |
| Gray et al. Cloning, nucleotide sequence, and expression in Escherichia coli of the exotoxin A structural gene of Pseudomonas aeruginosa. Proc Natl Acad Sci, vol. 81, pp. 2645-2649 (May 1984). |
| Kim et al. Induction of anti-inflammatory immune response by an adenovirus vector encoding 11 tandem repeats of Aβ1-6: Toward safer and effective vaccines against Alzheimer's disease. Biochemical and Biophysical Research Communications 336:84-92 (2005). Available online Aug. 19, 2005. |
| PCT/US2019/050708 International Preliminary Report on Patentability dated May 11, 2021. |
| PCT/US2021/032097 International Search Report and Written Opinion dated Jul. 30, 2021. |
| U.S. Appl. No. 17/004,686 Office Action dated Jul. 14, 2021. |
| U.S. Appl. No. 17/129,376 Office Action dated Jun. 29, 2021. |
| Co-pending U.S. Appl. No. 17/129,376, inventors Hunter; Thomas Carl et al., filed Dec. 21, 2020. |
| Aman et al. A mutant cholera toxin B subunit that binds GM1-ganglioside but lacks immunomodulatory or toxic activity. PNAS 98(15):8536-8541 (Jul. 17, 2001). |
| Anselmo et al. Non-invasive delivery strategies for biologies. Nature Reviews Drug Discovery 18:19-40 (Jan. 2019). Published online Nov. 30, 2018. |
| Apostolaki et al. Nasal Delivery of Antigen with the B Subunit of Escherichia coli Heat-Labile Enterotoxin Augments Antigen-Specific T-Cell Clonal Expansion and Differentiation. Infection and Immunity 72(7):4072-4080 (Jul. 2004). DOI: 10.1128/IAI.72.7.4072-4080.2004. |
| Arbit et al. Oral Insulin Delivery in a Physiologic Context: Review. J Diabetes Sci Technol 11(4):825-832 (Jul. 2017) Epub Feb. 2, 2017. |
| Arhewoh et al. An overview of site-specific delivery of orally administered proteins/peptides and modelling considerations. JMBR: A Peer-review Journal of Biomedical Sciences 3(1):7-20 (Jun. 2004). |
| Awasthi et al. Development of a PCR-restriction fragment length polymorphism assay for detection and subtyping of cholix toxin variant genes of Vibrio cholerae. Journal of Medical Microbiology 63(5):667-673 (May 1, 2014). DOI: 10.1099/jmm.0.070797-0. |
| Awasthi et al. Novel Cholix Toxin Variants, ADP-Ribosylating Toxins in Vibriocholerae Non-O1/Non-O139 Strains, and Their Pathogenicity. Infection and Immunity 81(2):531-541 (Feb. 2013). Published ahead of print Dec. 10, 2012. |
| Basset et al. Cholera-Like Enterotoxins and Regulatory T cells. Toxins 2:1774-1795 (Jul. 6, 2010). doi: 10.3390/toxins2071774. |
| Bishop-Lilly et al. Genome Sequencing of 15 Clinical Vibrio Isolates, Including 13 Non-O1/Non-O139 Serogroup Strains.Genome Announc 2(5):e00893-14 (Sep. 11, 2014). doi:10.1128/genomeA.00893-14. |
| Boirivant et al. Oral Administration of Recombinant Cholera Toxin Subunit B Inhibits IL-12-Mediated Murine Experimental (Trinitrobenzene Sulfonic Acid) Colitis. J Immunol 166:3522-3532 (2001). doi: 10.4049/jimmunol.166.5.3522. |
| Bonissone et al. N-terminal Protein Processing: A Comparative Proteogenomic Analysis. Molecular & Cellular Proteomics 12: 10.1074/mcp.M112.019075, 14-28 (2013). |
| Bourganis et al. Polyelectrolyte complexes as prospective carriers for the oral delivery of protein therapeutics. European Journal of Pharmaceutics and Biopharmaceutics 111:44-60 (2017). Available online Nov. 12, 2016. |
| Bublin et al. Use of a genetic cholera toxin B subunit/allergen fusion molecule as mucosal delivery system with immunosuppressive activity against Th2 immune responses. Vaccine 25(50):8395-8404 (Dec. 5, 2007). DOI: https://doi.org/10.1016/j.vaccine.2007.10.003. Available online Oct. 22, 2007. |
| Choonara et al. A review of advanced oral drug delivery technologies facilitating the protection and absorption of protein and peptide molecules. Biotechnology Advances 32:1269-1282 (2014). Available online Aug. 3, 2014. |
| Co-pending U.S. Appl. No. 16/779,350, inventors Liu; Keyi et al., filed Jan. 31, 2020. |
| Co-pending U.S. Appl. No. 16/884,456, inventors Mrsny; Randall J. et al., filed May 27, 2020. |
| Co-pending U.S. Appl. No. 16/997,781, inventors Mrsny; Randall J. et al., filed Aug. 19, 2020. |
| Co-pending U.S. Appl. No. 17/004,686, inventors Mrsny; Randall J. et al., filed Aug. 27, 2020. |
| Crowe et al. Oral delivery of the anti-tumor necrosis factor α domain antibody, V565, results in high intestinal and fecal concentrations with minimal systemic exposure in cynomolgus monkeys. Drug Development and Industrial Pharmacy 45(3):387-394 (2019). Accepted author version posted online Nov. 5, 2018. Published online Nov. 25, 2018. |
| Date et al. Nanoparticles for oral delivery: Design, evaluation and state-of-the-art. Journal of Controlled Release 240:504-526 (Oct. 28, 2016). |
| Delie et al. Polymeric Particulates to Improve Oral Bioavailability of Peptide Drugs. Molecules 10(1):65-80 (Jan. 31, 2005). |
| Donaldson et al. Mucosal administration of the B subunit of E. coli heat-labile enterotoxin promotes the development of Foxp3-expressing regulatory T cells. Mucosal Immunology 4(2):227-238 (Mar. 2011). Published online Oct. 13, 2010. doi: 10.1038/mi.2010.65. |
| Donaldson et al. The Escherichia coli heat-labile enterotoxin B subunit protects from allergic airway disease development by inducing CD4+ regulatory T cells. Mucosal Immunology 6(3):535-546 (May 2013). Published online Oct. 3, 2012. doi: 10.1038/mi.2012.93. |
| Fitzgerald, et al. Pseudomonas exotoxin-mediated selection yields cells with altered expression of low-density lipoprotein receptor-related protein. Journ of Cell Biology, 129.6 (1995): 1533-1541. |
| Fraser et al. Mutant Escherichia coli Heat-Labile Toxin B Subunit That Separates Toxoid-Mediated Signaling and Immunomodulatory Action from Trafficking and Delivery Functions. Infection and Immunity 71(3):1527-1537 (Mar. 2003). DOI: 10.1128/IAI.71.3.000-000.2003. |
| GenBank Accession No. AAW80252. Version No. AAW80252.1 hypothetical exotoxin A [Vibrio cholerae]. Record created Feb. 9, 2005. 2 pages. Retrieved Nov. 11, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/58615288?report=ipg. |
| GenBank Accession No. AKB06426. Version No. AKB06426.1. exotoxin A catalytic family protein [Vibrio cholerae]. Record created Apr. 6, 2015. 2 pages. Retrieved Aug. 30, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/AKB06426. |
| GenBank Accession No. ALH24940. Version No. ALH24940.1. cholix toxin [Vibrio cholerae]. Record created Oct. 11, 2015. 2 pages. Retrieved Sep. 6, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/ALH24940.1. |
| GenBank Accession No. ALI16365. Version No. ALI16365.1. truncated cholix toxin [Vibrio cholerae]. Record created Oct. 12, 2015. 2 pages. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/ALI16365.1. |
| GenBank Accession No. ALI16366. Version No. ALI16366.1. truncated cholix toxin [Vibrio cholerae]. Record created Oct. 12, 2015. 2 pages. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/ALI16366.1. |
| GenBank Accession No. ALI87044. Version No. ALI87044.1. cholix toxin [Vibrio cholerae]. Record created Oct. 14, 2015. 2 pages. Retrieved Aug. 30, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/ALI87044.1. |
| GenBank Accession No. ALJ02941. Version No. ALJ02941.1. cholix toxin [Vibrio cholerae]. Record created Oct. 18, 2015. 2 pages. Retrieved Sep. 6, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/ALJ02941.1. |
| GenBank Accession No. AUT32289. Version No. AUT32289.1. cholix toxin [Vibrio cholerae]. Record created Jan. 31, 2018. 2 pages. Retrieved Sep. 6, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/AUT32289.1. |
| GenBank Accession No. AUT32291. Version No. AUT32291.1. cholix toxin [Vibrio cholerae]. Record created Jan. 31, 2018. 2 pages. Retrieved Sep. 6, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/AUT32291.1. |
| GenBank Accession No. AUT32293. Version No. AUT32293.1. cholix toxin [Vibrio cholerae]. Record created Jan. 31, 2018. 2 pages. Retrieved Sep. 6, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/AUT32293.1. |
| GenBank Accession No. AUT32294. Version No. AUT32294.1. cholix toxin [Vibrio cholerae]. Record created Jan. 31, 2018. 2 pages. Retrieved Sep. 6, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/AUT32294.1. |
| GenBank Accession No. BAM72568. Version No. BAM72568.1. cholix toxin, partial [Vibrio cholerae]. Record created Dec. 14, 2012. 2 pages. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/BAM72568.1. |
| GenBank Accession No. BAM72569. Version No. BAM72569.1. cholix toxin, partial [Vibrio cholerae]. Record created Dec. 14, 2012. 2 pages. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/BAM72569.1. |
| GenBank Accession No. BAM72570. Version No. BAM72570.1. cholix toxin, partial [Vibrio cholerae]. Record created Dec. 14, 2012. 2 pages. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/BAM72570.1. |
| GenBank Accession No. BAM72571. Version No. BAM72571.1. cholix toxin, partial [Vibrio cholerae]. Record created Dec. 14, 2012. 2 pages. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/BAM72571.1. |
| GenBank Accession No. BAM72573. Version No. BAM72573.1. cholix toxin, partial [Vibrio cholerae]. Record created Dec. 14, 2012. 2 pages. Retrieved Sep. 6, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/BAM72573.1. |
| GenBank Accession No. BAM72574. Version No. BAM72574.1. cholix toxin, partial [Vibrio cholerae]. Record created Dec. 14, 2012. 2 pages. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/BAM72574.1. |
| GenBank Accession No. BAM72575. Version No. BAM72575.1. cholix toxin, partial [Vibrio cholerae]. Record created Dec. 14, 2012. 2 pages. Retrieved Sep. 6, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/BAM72575.1. |
| GenBank Accession No. BAM72576. Version No. BAM72576.1. cholix toxin, partial [Vibrio cholerae]. Record created Dec. 14, 2012. 2 pages. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/BAM72576.1. |
| GenBank Accession No. BAM72582. Version No. BAM72582.1. cholix toxin, partial [Vibrio cholerae]. Record created Dec. 14, 2012. 2 pages. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/BAM72582.1. |
| GenBank Accession No. BAM72585. Version No. BAM72585.1. cholix toxin, partial [Vibrio cholerae]. Record created Dec. 14, 2012. 2 pages. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/BAM72585.1. |
| GenBank Accession No. BAM72587. Version No. BAM72587.1. cholix toxin, partial [Vibrio cholerae]. Record created Dec. 14, 2012. 2 pages. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/BAM72587.1. |
| GenBank Accession No. BAM72590. Version No. BAM72590.1. cholix toxin, partial [Vibrio cholerae]. Record created Dec. 14, 2012. 2 pages. Retrieved Sep. 6, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/BAM72590.1. |
| GenBank Accession No. BAM72593. Version No. BAM72593.1. cholix toxin, partial [Vibrio cholerae]. Record created Dec. 14, 2012. 2 pages. Retrieved Sep. 6, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/BAM72593.1. |
| GenBank Accession No. BAM72594. Version No. BAM72594.1. cholix toxin, partial [Vibrio cholerae]. Record created Dec. 14, 2012. 2 pages. Retrieved Sep. 6, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/BAM72594.1. |
| GenBank Accession No. BAM72595. Version No. BAM72595.1. cholix toxin, partial [Vibrio cholerae]. Record created Dec. 14, 2012. 2 pages. Retrieved Sep. 6, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/BAM72595.1. |
| GenBank Accession No. BAM72596. Version No. BAM72596.1. cholix toxin, partial [Vibrio cholerae]. Record created Dec. 14, 2012. 2 pages. Retrieved Sep. 6, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/BAM72596.1. |
| GenBank Accession No. BAM72610. Version No. BAM72610.1. cholix toxin, partial [Vibrio cholerae]. Record created Dec. 14, 2012. 2 pages. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/BAM72610.1. |
| GenBank Accession No. BAM72611. Version No. BAM72611.1. cholix toxin, partial [Vibrio cholerae]. Record created Dec. 14, 2012. 2 pages. Retrieved Sep. 6, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/BAM72611.1. |
| GenBank Accession No. EFH75651. Version No. EFH75651.1. conserved hypothetical protein [Vibrio cholerae RC385]. Record created Jun. 4, 2010. 2 pages. Retrieved Sep. 6, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/EFH75651.1. |
| GenBank Accession No. KFD89501. Version No. KFD89501.1. exotoxin A binding family protein [Vibrio cholerae]. Record created Jul. 31, 2014. pages. Retrieved Sep. 6, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/KFD89501.1. |
| GenBank Accession No. KFD96741. Version No. KFD96741.1. exotoxin A binding family protein [Vibrio cholerae]. Record created Jul. 31, 2014. 2 pages. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/KFD96741.1. |
| GenBank Accession No. KFE28160. Version No. KFE28160.1. exotoxin A binding family protein [Vibrio cholerae]. Record created Jul. 31, 2014. 2 pages. Retrieved Sep. 6, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/KFE28160.1. |
| GenBank Accession No. KNH55243. Version No. KNH55243.1. hypothetical protein A59_2898 [Vibrio cholerae 623-39]. Record created Aug. 5, 2015. 2 pages. Retrieved Sep. 6, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/KNH55243.1. |
| GenBank Accession No. P01241. Somatotropin. Record created Jul. 21, 1986. 12 pages. Retrieved Aug. 29, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/P01241. |
| GenBank Accession No. Q5EK40. Version No. Q5EK40.1. Cholix toxin. Record created Feb. 9, 2005. 9 pages. Retrieved Aug. 30, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/Q5EK40.1. |
| GenBank Accession No. SYZ81493. Version No. SYZ81493.1. Cholix toxin precursor [Vibrio cholerae]. Record created Sep. 6, 2018. 1 page. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/SYZ81493.1. |
| GenBank Accession No. WP_000941100. Version No. WP_000941100.1. Multispecies: cholix toxin [Vibrio]. Record created Feb. 5, 2013. 1 page. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_000941100.1. |
| GenBank Accession No. WP_002044040. Version No. WP_002044040.1. cholix toxin [Vibrio cholerae]. Record created May 4, 2013. 1 page. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_002044040.1. |
| GenBank Accession No. WP_032467916. Version No. WP_032467916.1. cholix toxin [Vibrio cholerae]. Record created Oct. 4, 2014. 1 page. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_032467916.1. |
| GenBank Accession No. WP_032482668. Version No. WP_032482668.1. cholix toxin [Vibrio cholerae]. Record created Oct. 4, 2014. 1 page. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_032482668.1. |
| GenBank Accession No. WP_033932701. Version No. WP_033932701.1. cholix toxin [Vibrio cholerae]. Record created Dec. 5, 2014. 1 page. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_033932701.1. |
| GenBank Accession No. WP_042988437. Version No. WP_042988437.1. cholix toxin [Vibrio cholerae]. Record created Feb. 17, 2015. 1 page. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_042988437.1. |
| GenBank Accession No. WP_057552180. Version No. WP_057552180.1. cholix toxin [Vibrio cholerae]. Record created Nov. 10, 2015. 1 page. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_057552180.1. |
| GenBank Accession No. WP_057557199. Version No. WP_057557199.1. cholix toxin [Vibrio cholerae]. Record created Nov. 10, 2015. 1 page. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_057557199.1. |
| GenBank Accession No. WP_069648100. Version No. WP_069648100.1. cholix toxin [Vibrio cholerae]. Record created Sep. 20, 2016. 1 page. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_069648100.1. |
| GenBank Accession No. WP_071178365. Version No. WP_071178365.1. cholix toxin [Vibrio cholerae]. Record created Nov. 2, 2016. 1 page. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_071178365.1. |
| GenBank Accession No. WP_071186455. Version No. WP_071186455.1. cholix toxin [Vibrio cholerae]. Record created Nov. 2, 2016. 1 page. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_071186455.1. |
| GenBank Accession No. WP_076008260. Version No. WP_076008260.1. cholix toxin [Vibrio cholerae]. Record created Jan. 19, 2017. 1 page. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_076008260.1. |
| GenBank Accession No. WP_076025263. Version No. WP_076025263.1. cholix toxin [Vibrio cholerae]. Record created Jan. 19, 2017. 1 page. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_076025263.1. |
| GenBank Accession No. WP_084980904. Version No. WP_084980904.1. cholix toxin [Vibrio cholerae]. Record created Apr. 21, 2017. 1 page. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_084980904.1. |
| GenBank Accession No. WP_088131881. Version No. WP_088131881.1. cholix toxin [Vibrio cholerae]. Record created Jun. 19, 2017. 1 page. Retrieved Sep. 6, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_088131881.1. |
| GenBank Accession No. WP_095461883. Version No. WP_095461883.1. cholix toxin [Vibrio cholerae]. Record created Sep. 2, 2017. 1 page. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_095461883.1. |
| GenBank Accession No. WP_095463544. Version No. WP_095463544.1. cholix toxin [Vibrio cholerae]. Record created Sep. 2, 2017. 1 page. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_095463544.1. |
| GenBank Accession No. WP_095466115. Version No. WP_095466115.1. cholix toxin [Vibrio cholerae]. Record created Sep. 2, 2017. 1 page. Retrieved Sep. 6, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_095466115.1. |
| GenBank Accession No. WP_095473667. Version No. WP_095473667.1. cholix toxin [Vibrio cholerae]. Record created Sep. 2, 2017. 1 page. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_095473667.1. |
| GenBank Accession No. WP_095477173. Version No. WP_095477173.1. cholix toxin [Vibrio cholerae]. Record created Sep. 2, 2017. 1 page. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_095477173.1. |
| GenBank Accession No. WP_095490358. Version No. WP_095490358.1. cholix toxin [Vibrio cholerae]. Record created Sep. 2, 2017. 1 page. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_095490358.1. |
| GenBank Accession No. WP_113605545. Version No. WP_113605545.1. cholix toxin [Vibrio sp. 2017V-1105]. Record created Jul. 15, 2018. 1 page. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_113605545.1. |
| GenBank Accession No. WP_113620122. Version No. WP_113620122.1. cholix toxin [Vibrio sp. 2014V-1107]. Record created Jul. 15, 2018. 1 page. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_113620122.1. |
| GenBank Accession No. WP_113628761. Version No. WP_113628761.1. cholix toxin [Vibrio cholerae]. Record created Jul. 15, 2018. 1 page. Retrieved Sep. 6, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_113628761.1. |
| GenBank Accession No. WP_114707943. Version No. WP_114707943.1. cholix toxin [Vibrio cholerae]. Record created Aug. 2, 2018. 1 page. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_114707943.1. |
| GenBank Accession No. WP_114708586. Version No. WP_114708586.1. cholix toxin [Vibrio cholerae]. Record created Aug. 2, 2018. 1 page. Retrieved Sep. 6, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_114708586.1. |
| GenBank Accession No. WP_1 14711324. Version No. WP_114711324.1. cholix toxin [Vibrio cholerae]. Record created Aug. 2, 2018. 1 page. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_114711324.1. |
| GenBank Accession No. WP_114718037. Version No. WP_114718037.1. cholix toxin [Vibrio cholerae]. Record created Aug. 2, 2018. 1 page. Retrieved Sep. 6, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_114718037.1. |
| GenBank Accession No. WP_114728533. Version No. WP_114728533.1. cholix toxin [Vibrio cholerae]. Record created Aug. 2, 2018. 2 pages. Retrieved Sep. 6, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_114728533.1. |
| GenBank Accession No. WP_114735885. Version No. WP_114735885.1. cholix toxin [Vibrio cholerae]. Record created Aug. 2, 2018. 1 page. Retrieved Sep. 6, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_114735885.1. |
| GenBank Accession No. WP_114741531. Version No. WP_114741531.1. cholix toxin [Vibrio cholerae]. Record created Aug. 2, 2018. 1 page. Retrieved Sep. 6, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_114741531.1. |
| GenBank Accession No. WP_114743333. Version No. WP_114743333.1. cholix toxin [Vibrio cholerae]. Record created Aug. 2, 2018. 1 page. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_114743333.1. |
| GenBank Accession No. WP_114774300. Version No. WP_114774300.1. cholix toxin [Vibrio cholerae]. Record created Aug. 2, 2018. 1 page. Retrieved Sep. 6, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_114774300.1. |
| GenBank Accession No. WP_114776277. Version No. WP_114776277.1. cholix toxin [Vibrio cholerae]. Record created Aug. 2, 2018. 1 page. Retrieved Sep. 6, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_114776277.1. |
| GenBank Accession No. WP_114788528. Version No. WP_114788528.1. cholix toxin, partial [Vibrio cholerae]. Record created Aug. 2, 2018. 1 page. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_114788528.1. |
| GenBank Accession No. WP_114794357. Version No. WP_114794357.1. cholix toxin [Vibrio cholerae]. Record created Aug. 2, 2018. 1 page. Retrieved Sep. 6, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_114794357.1. |
| GenBank Accession No. WP_114808068. Version No. WP_114808068.1. cholix toxin [Vibrio cholerae]. Record created Aug. 2, 2018. 1 page. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_114808068.1. |
| GenBank Accession No. WP_114967888. Version No. WP_114967888.1. cholix toxin [Vibrio cholerae]. Record created Aug. 3, 2018. 1 page. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_114967888.1. |
| GenBank Accession No. WP_114974465. Version No. WP_114974465.1. cholix toxin [Vibrio cholerae]. Record created Aug. 3, 2018. 1 page. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_114974465.1. |
| GenBank Accession No. WP_119788544. Version No. WP_119788544.1. cholix toxin [Vibrio cholerae]. Record created Sep. 26, 2018. 1 page. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_119788544.1. |
| GenBank Accession No. WP_123013236. Version No. WP_123013236.1. cholix toxin [Vibrio cholerae]. Record created Nov. 10, 2018. 1 page. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_123013236.1. |
| GenBank Accession No. WP_123162729. Version No. WP_123162729.1. cholix toxin [Vibrio cholerae]. Record created Nov. 14, 2018. 1 page. Retrieved Sep. 9, 2019 at URL: https://www.ncbi.nlm.nih.gov/protein/WP_123162729.1. |
| Ghosh et al. Peptides as drug delivery vehicles across biological barriers. Journal of Pharmaceutical Investigation 48:89-111 (Jan. 2018). Published online Dec. 12, 2017. |
| Gupta, et al. Permeation of insulin, calcitonin and exenatide across Caco-2 monolayers: measurement using a rapid, 3-day system. PloS one 8.2 (2013): e57136. |
| Hajishengallis et al. Type II Heat-labile Enterotoxins: Structure, Function, and Immunomodulatory Properties. Vet Immunol Immunopathol 152(1-2):68-77 (Mar. 15, 2013). doi:10.1016/j.vetimm.2012.09.034. |
| Hsu, et al. Vaccination against Gonadotropin-releasing Hormone (GnRH). Cancer Res. Jul. 15, 2000; 60:3701-3705. |
| Ji et al. The B subunit of Escherichia coli heat-labile toxin alters the development and antigen-presenting capacity of dendritic cells. J Cell Mol Med 19(8):2019-2031 (2015). doi: 10.1111/jcmm.12599. |
| Johnson et al. Complete Genome Assemblies for Two Single-Chromosome Vibrio cholerae Isolates, Strains 1154-74 (Serogroup O49) and 10432-62 (Serogroup O27). Genome Announc 3(3):e00462-15 (May 14, 2015). 2 pages. doi:10.1128/genomeA.00462-15. |
| J∅rgensen, et al. Cholix toxin, a novel ADP-ribosylating factor from Vibrio cholerae. Journal of Biological Chemistry 283.16 (Apr. 18, 2008): 10671-10678. |
| Killeen, et al. Conformational integrity of a recombinant toxoid of Pseudomonas aeruginosa exotoxin A containing a deletion of glutamic acid-553. Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1138.2 (1992): 162-166. |
| Kondo et al. Activity of immunotoxins constructed with modified Pseudomonas exotoxin A lacking the cell recognition domain. J Biol Chem 263(19):9470-9475 (Jul. 5, 1988). |
| Kumar et al. Genome Sequence of Non-O1 Vibrio cholerae PS15. Genome Announcements 1(1):e00227-12 (Jan./Feb. 2013). 2 pages. |
| Laurent. Characterization of the trafficking pathway used by Pseudomonas aeruginosa Exotoxin A and application to oral drug delivery. Ph.D. Thesis. University of Bath. Dec. 2015. Retrieved Dec. 18, 2019 from URL: https://purehost.bath.ac.uk/ws/portalfiles/portal/187920618/Thesis_F.Laurent_Dec2015.pdf. 312 pages. |
| Lueben et al. Mucoadhesive Polymers in Peroral Peptide Drug Delivery. II. Carbomer and Polycarbophil Are Potent Inhibitors of the Intestinal Proteolytic Enzyme Trypsin. Pharmaceutical Research 12(9):1293-1298 (1995). |
| Lugo et al. The Father, Son and Cholix Toxin: The Third Member of the DT Group Mono-ADP-Ribosyltransferase Toxin Family. Toxins 7(8):2757-2772 (Jul. 24, 2015). |
| Luross et al. Escherichia coli Heat-Labile Enterotoxin B Subunit Prevents Autoimmune Arthritis Through Induction of Regulatory CD4+ T Cells. Arthritis & Rheumatism 46(6):1671-1682 (Jun. 6, 2002). DOI 10.1002/art. 10328. |
| Mahato et al. Emerging trends in oral delivery of peptide and protein drugs. Crit Rev Ther Drug Carrier Syst. 2003;20(2-3):153-214. |
| Mattoo et al. Interactions of bacterial effector proteins with host proteins. Curr Opin Immunol. Aug. 2007;19(4):392-401. |
| Mekalanos et al. Cholera toxin genes: nucleotide sequence, deletion analysis and vaccine development. Nature 306:551-557 (1983). |
| Merritt et al. Crystal structure of cholera toxin B-pentamer bound to receptor GM1 pentasaccharide. Protein Science 3:166-175 (1994). |
| Milling et al. Regulation of intestinal immunity: Effects of the oral adjuvant Escherichia coli heat-labile enterotoxin on heat-labile enterotoxin on migrating dendritic cells. Eur. J. Immunol. 37:87-99 (2007). DOI 10.1002/eji.200636199. |
| Moroz, et al. Oral delivery of macromolecular drugs: Where we are after almost 100years of attempts. Adv Drug Deliv Rev. Jun. 1, 2016;101:108-121. |
| Mrsny. Biotech Start-up—A Practical Guide. Bath, United Kingdom (Presentation.) (Nov. 19, 2018.) 18 pages. |
| Mrsny. Breaking Through the Biological Barriers that Limit Protein Drug Delivery. Bangor University, United Kingdom (Presentation.) (Aug. 6, 2015.) 26 pages. |
| Mrsny. Breaking Through the Biological Barriers that Limit Protein Drug Delivery. (Presentation.) Controlled Release Society, Florence, Italy (Nov. 8, 2014.) 43 pages. |
| Mrsny. Breaking Through the Biological Barriers that Limit Protein Drug Delivery. (Presentation.) Tours, France (Jul. 2, 2015.) 25 pages. |
| Mrsny. Employing endogenous pathways for the oral delivery of biopharmaceuticals. (Presentation.) Reading, United Kingdom (Jul. 18, 2018.) 35 pages. |
| Mrsny, et al. Bacterial toxins as tools for mucosal vaccination. Drug Discovery Today. 2002; 4:247-258. |
| Mrsny et al. Mucosal administration of a chimera composed of Pseudomonas exotoxin and the gp120 V3 loop sequence of HIV-1 induces both salivary and serum antibody responses. Vaccine 17(11-12):1425-1433 (Mar. 17, 1999). |
| Mrsny. Harnessing Mucosal Immunology for Health. Bath, United Kingdom (Presentation.) (Sep. 25, 2018.) 29 pages. |
| Mrsny. Harnessing Mucosal Immunology for Health. Ma'alot-Tarshiha, Israel (Presentation.) (Oct. 7, 2018.) 28 pages. |
| Mrsny, Lessons from nature: “Pathogen-Mimetic” systems for Mucosal Nano-medicines, Advanced Drug Delivery Reviews, vol. 61 :172-192 (online Dec. 24, 2008). |
| Mrsny. Molecular mechanisms of transcytosis pathways: Drug delivery thru epithelial and endothelial barriers. (Presentation.) (Dec. 3, 2010). 42 pages. |
| Mrsny. Molecular mechanisms of transcytosis pathways: Drug delivery thru epithelial and endothelial barriers. (Presentation.) Emory University, Atlanta, GA, United States. (Sep. 24, 2010). 51 pages. |
| Mrsny. Molecular mechanisms of transcytosis pathways: Drug delivery thru epithelial and endothelial barriers. (Presentation.) Nanomedicine and Drug Delivery Symposium (NanoDDS), University of Nebraska Omaha, Omaha, NE, United States. (Oct. 3, 2010.) 42 pages. |
| Mrsny. My Secondment(Gap Years?) at AMT. University of Bath, United Kingdom(Presentation.) (Oct. 6, 2017.) 20 pages. |
| Mrsny. Overcoming Barriers to Oral Protein Delivery. Boston, MA, United States (Presentation.) (Jul. 23, 2018.) 35 pages. |
| Mrsny. Overcoming Biological Barriers that Limit Peptide and Protein Drug Delivery. Berlin, Germany (Presentation.) (May 23, 2016.) 26 pages. |
| Mrsny. Overcoming Biological Barriers that Limit Peptide and Protein Drug Delivery. Denver, CO, United States (Presentation.) (Nov. 17, 2016.) 15 pages. |
| Mrsny. Overcoming Biological Barriers that Limit Peptide and Protein Drug Delivery. (Presentation.) (Jun. 14, 2016.) 36 pages. |
| Mrsny. Overcoming Biological Barriers that Limit Peptide and Protein Drug Delivery. University of California San Francisco, CA, United States (Presentation.) (Mar. 24, 2016.) 36 pages. |
| Mrsny. Paracellular and Transcellular Strategies to Enhance Oral Protein Delivery. (Presentation.) San Francisco, CA, United States (Mar. 15, 2013.) 41 pages. |
| Mrsny. Paracellular and Transcellular Strategies to Enhance Oral Protein Delivery. (Presentation.) Seoul, South Korea (Mar. 15, 2012.) 54 pages. |
| Mrsny. Paracellular and Transcellular Strategies to Enhance Oral Protein Delivery. (Presentation.) University of California, Santa Barbara, CA, United States. (Feb. 26, 2013.) 54 pages. |
| Mrsny. Permeation of barriers for GI and pulmonary drug delivery. (Presentation.) Gordon Research Conference, New Hampshire, United States. (Aug. 13, 2012.) 46 pages. |
| Mrsny. Prospects for Oral Delivery of Peptide and Protein Therapeutics. San Francisco, CA, United States (Presentation.) (May 21, 2018.) 29 pages. |
| Mrsny. Prospects for Oral Delivery of Peptide and Protein Therapeutics. University of Nottingham, United Kingdom(Presentation.) (Jun. 20, 2018.) 62 pages. |
| Mrsny. Strategies to Enhance the Oral Delivery of Therapeutic Proteins and Peptides. (Presentation.) Berlin, Germany. (Sep. 28, 2011.) 42 pages. |
| Mrsny. Strategies to Enhance the Oral Delivery of Therapeutic Proteins and Peptides. (Presentation.) Dunedin, New Zealand (Feb. 15, 2012). 42 pages. |
| Mrsny. Strategies to Enhance the Oral Delivery of Therapeutic Proteins and Peptides. (Presentation.) Nottingham, United Kingdom. (Sep. 2, 2011.) 42 pages. |
| Mrsny. Strategies to Enhance the Oral Delivery of Therapeutic Proteins and Peptides. (Presentation.) San Francisco, CA, United States. (Jun. 20, 2011.) 42 pages. |
| Mrsny. Strategies to Enhance the Oral Delivery of Therapeutic Proteins and Peptides. (Presentation.) The University of Sheffield, Sheffield, United Kingdom. (Jan. 16, 2012.) 42 pages. |
| Mrsny. TJ Regulation using Cell-Penetrating Peptides. (Presentation.) University of Copenhagen, Denmark (May 12, 2015.) 62 pages. |
| Mrsny. Understanding & Developing the Science Behind Oral Protein and Peptide Delivery. (Presentation.) Nottingham, United Kingdom (Jan. 22, 2014.) 48 pages. |
| Mrsny. Understanding & Developing the Science Behind Oral Protein Delivery: An Academic Case Study. (Presentation.) Berlin, Germany (Feb. 20, 2013.) 39 pages. |
| Mrsny. Understanding & Developing the Science Behind Oral Protein Delivery. (Presentation.) University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, United States. (May 28, 2014.) 37 pages. |
| Mrsny. Understanding & Developing the Science Behind Oral Protein Delivery. (Presentation.) University of Westminster, London, United Kingdom. (Mar. 15, 2013). 40 pages. |
| Mrsny. Understanding & Developing the Science Behind Oral Protein Delivery. (Presentation.) Academy of Pharmaceutical Sciences, Edinburgh, United Kingdom.(Sep. 3, 2013). 40 pages. |
| Mrsny. Understanding & Developing the Science Behind Oral Protein Delivery. (Presentation.) University College Dublin, Dublin, lreland(May 22, 2013). 44 pages. |
| Mrsny. Understanding & Developing the Science Behind Oral Protein Delivery. (Presentation.) University of East Anglia, Norwich, United Kingdom(Jun. 27, 2013). 43 pages. |
| Mrsny. Understanding Exotoxin Transcytosis for the Application of Oral Protein Delivery. Dresden, Germany (Presentation.) (Nov. 12, 2015.) 26 pages. |
| Mudrak et al. Heat-Labile Enterotoxin: Beyond GM1 Binding. Toxins 2:1445-1470 (Jun. 14, 2010). doi:10.3390/toxins2061445. |
| Pastan et al. Recombinant Toxins as Novel Therapeutic Agents. Annu Rev Biochem 61:331-54 (1992). |
| Plant et al. Modulation of the Immune Response by the Cholera-like Enterotoxins. Current Topics in Medicinal Chemistry 4:509-519 (2004). |
| Plant et al. The B subunit of Escherichia coli heat labile enterotoxin abrogates oral tolerance, promoting predominantly Th2-type immune responses. Eur J Immunol 33:3186-3195 (2003). |
| Porat. Accelerating Development of a Novel Chimera Protein through the Identification of a Two Column Purification Process Using NH2-750F and CaPure Resins. San Francisco, CA, United States.(Presentation.) (Nov. 7, 2018.) 30 pages. |
| Purdy et al. A Glimpse into the Expanded Genome Content of Vibrio cholerae through Identification of Genes Present in Environmental Strains. Journal of Bacteriology 187(9):2992-3001 (May 2005).DOI: 10.1128/JB.187.9.2992-3001.2005. |
| Purdy et al. Diversity and distribution of cholixtoxin, a novel ADP-ribosylating factor from Vibrio cholerae. Environmental Microbiology Reports 2(1):198-207 (Feb. 2010). First published Feb. 8, 2010. DOI: https://doi.org/10.1111/j.1758-2229.2010.00139.x. |
| Raveney et al. The B Subunit of Escherichia coli Heat-Labile Enterotoxin Inhibits Th1 but Not Th17 Cell Responses in Established Experimental Autoimmune Uveoretinitis. Investigative Ophthalmology & Visual Science 49(9):4008-4017 (Sep. 2008). |
| Rodighiero, et al. Structural Basis for the Differential Toxicity of Cholera Toxin and Escherichia coli Heat-labile Enterotoxin. The Journal of Biological Chemistry 274.77 (1999):3962-3969. |
| Rubas et al. Flux Measurements across Caco-2 Monolayers May Predict Transport in Human Large Intestinal Tissue. J Pharm Sci 85(2):165-169 (Feb. 1996). |
| Rubas et al. An integrated method to determine epithelial transport and bioactivity of oral drug candidates in vitro. Pharm Res 13(1):23-26 (Jan. 1996). |
| Rubas et al. Comparison of the permeability characteristics of a human colonic epithelial (Caco-2) cell line to colon of rabbit, monkey, and dog intestine and human drug absorption. Pharm Res.10(1):113-118 (1993). |
| Ruddock et al. Assembly of the B Subunit Pentamer of Escherichia coli Heat-labile Enterotoxin. J Biol Chem 271(32):19118-19123 (Aug. 9, 1996). |
| Ruddock et al. Kinetics of Acid-mediated Disassembly of the B Subunit Pentamer of Escherichia coli Heat-labile Enterotoxin. J Biol Chem 270(50):29953-29958 (Dec. 15, 1995). |
| Saidi et al. Prevalence of Vibrio cholerae O1 EI Tor variant in a cholera-endemic zone of Kenya. Journal of Medical Microbiology 63:415-420 (2014). First published online Mar. 1, 2014. doi:10.1099/jmm.0.068999-0. |
| Salmond et al. The B Subunit of Escherichia coli Heat-Labile Enterotoxin Induces Both Caspase-Dependent and -Independent Cell Death Pathways in CD8+ T Cells. Infection and Immunity 72(10):5850-5857 (Oct. 2004). |
| Sarnovsky, et al. Initial characterization of an immunotoxin constructed from domains II and III of cholera exotoxin. Cancer Immunol. Immunother., 59.5 2010 (published online Nov. 2009):737-746. |
| Schauer. AVX-470, an Orally-Delivered GI-Targeted anti-TNF for the Treatment of Pediatric IBD. Presentation. Avaxia Biologies (Oct. 26, 2015). 42 pages. |
| Shi et al. Oral delivery of human growth hormone: Preparation, characterization, and pharmacokinetics. J Biomater Appl 31(6):851-858 (Jan. 2017). Epub Oct. 14, 2016. |
| Shiraishi et al. Enhanced delivery of cell-penetrating peptide-peptide nucleic acid conjugates by endosomal disruption. Nat Protoc. 2006;1(2):633-6.Published online Jun. 29, 2006. doi: 10.1038/nprot.2006.92. |
| Siegall et al. Functional Analysis of Domains II, Ib, and III of Pseudomonas Exotoxin. J Biol Chem 264(24):14256-14261 (Aug. 25, 1989). |
| Simmons et al. Immunomodulation Using Bacterial Enterotoxins. Scand J Immunol 53:518-226 (2001). |
| Simon, et al. Novel bacterial ADP-ribosylating toxins: structure and function. Nature Reviews Microbiology 12.9 (2014): 599-611. |
| Song et al. Oral delivery system for low molecular weight protamine-dextran-poly(lactic-co-glycolic acid) carrying exenatide to overcome the mucus barrier and improve intestinal targeting efficiency. Nanomedicine (Lond.) 14(8):989-1009 (Apr. 2019). Published online Mar. 22, 2019. |
| Sun et al. Cholera toxin B subunit: An efficient transmucosal carrier-delivery system for induction of peripheral immunological tolerance. Proc Natl Acad Sci USA 91:10795-10799 (Nov. 1994). |
| Takeuchi et al. Mucoadhesive nanoparticulate systems for peptide drug delivery. Adv Drug Deliv Rev 47(1):39-54 (Mar. 23, 2001). |
| Taverner et al. Cholix protein domain I functions as a carrier element for efficient apical to basal epithelial transcytosis. Tissue Barriers, pp. 1710429-1 to 1710429-20 (Jan. 13, 2020). doi: 10.1080/21688370.2019.1710429. |
| Taverner, et al. Enhanced paracellular transport of insulin can be achieved via transient induction of myosin light chain phosphorylation. Journal of Controlled Release 210 (2015): 189-197. |
| Turcanu et al. Modulation of human monocytes by Escherichia coli heat-labile enterotoxin B-subunit; altered cytokine production and its functional consequences. Immunology 106:316-325 (2002). |
| U.S. Appl. No. 16/151,533 Notice of Allowance dated May 28, 2020. |
| U.S. Appl. No. 16/151,533 Notice of Allowance dated Sep. 8, 2020. |
| U.S. Appl. No. 16/207,655 Notice of Allowance dated Aug. 28, 2020. |
| U.S. Appl. No. 16/207,655 Notice of Allowance dated May 20, 2020. |
| U.S. Appl. No. 16/220,923 Notice of Allowance dated Aug. 27, 2020. |
| U.S. Appl. No. 16/220,923 Notice of Allowance dated May 20, 2020. |
| Wang et al. Methods to determine intestinal permeability and bacterial translocation during liver disease. J Immunol Methods 421:44-53 (Jun. 2015). Epub Jan. 13, 2015. doi:10.1016/j.jim.2014.12.015. |
| Wedekind et al. Refined crystallographic structure of Pseudomonas aeruginosa exotoxin A and its implications for the molecular mechanism of toxicity. J Mol Biol. Dec. 7, 2001;314(4):823-37. |
| Woodley, J.F. Enzymatic barriers for GI peptide and protein delivery. Crit Rev Ther Drug Carrier Syst. 1994;11(2-3):61-95. |
| Yahiro et al. Cholix toxin, an eukaryotic elongation factor 2 ADP-ribosyltransferase, interacts with Prohibitins and induces apoptosis with mitochondrial dysfunction in human hepatocytes. Cell Microbiol. Aug. 2019;21(8):e13033.doi: 10.1111/cmi.13033. Epub May 14, 2019. |
| Co-pending U.S. Appl. No. 17/558,418, inventors Mrsny; Randall J. et al., filed Dec. 21, 2021. |
| U.S. Appl. No. 16/884,456 Office Action dated Oct. 20, 2021. |
| U.S. Appl. No. 17/129,376 Office Action dated Oct. 6, 2021. |
| U.S. Appl. No. 16/884,456 Notice of Allowance dated Mar. 7, 2022. |
| Co-pending U.S. Appl. No. 17/684,619, inventors Mrsny; Randall J. et al., filed Mar. 2, 2022. |
| Co-pending U.S. Appl. No. 17/709,325, inventors Mrsny; Randall J. et al., filed Mar. 30, 2022. |
| Number | Date | Country | |
|---|---|---|---|
| 20210113704 A1 | Apr 2021 | US |
| Number | Date | Country | |
|---|---|---|---|
| 62640168 | Mar 2018 | US | |
| 62640188 | Mar 2018 | US | |
| 62640194 | Mar 2018 | US | |
| 62756889 | Nov 2018 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/US2019/021474 | Mar 2019 | US |
| Child | 17015011 | US |
