Patent Grant
11306306
The instant application contains a Sequence Listing which has been submitted electronically in ASCII format and is hereby incorporated by reference in its entirety. Said ASCII copy created on May 11, 2021, is named 50607_710_301_SL.txt and is 576,624 bytes in size.
Degrading proteins in a precise manner can be a key for controlling cellular functions. Many pathological conditions are characterized by aberrant functions of cellular pathways, either due to precocious protein expression or the expression of malfunctional variants. Thus, compounds that can specifically and precisely degrade the accumulation of such proteins or the malfunctioning faulty variants could be beneficial to treating various ailments. New technologies are being developed to discover and develop novel molecules to mediate protein degradation.
However, limited options exist to screen for molecules that accomplish functional degradation in an efficient manner. Accordingly, there is a need for development of methods and compositions that accomplish selective target protein degradation in precise and selective ways. The methods in this invention describe a screening platform that enables the creation of neosubstrates for specific E3 ligases by using compound libraries that are able to bridge an interaction between said E3 ligase and a target protein, leading to its degradation. The technology is amenable to various drug moieties, as well as DNA encoded libraries of peptides and macrocycles, which will mostly likely be close drug candidates due to their bivalent nature. The platform describes a selection approach, where only molecules that are able to yield functional target degradation are present.
Macrocyclic peptide natural products have been identified and isolated from a wide variety of species including bacteria, fungi, plants, algae, molluscs, and mammals. They are a recognized source of diverse biologically active molecules. Some cyclic peptides from marine sources have been approved by the Food and Drug Administration (FDA) such as ziconotide, a cyclic peptide isolated from the toxin of the cone snail species Conus magus. Ziconotide is an analgesic drug used for severe and chronic pain that works by selective blocking of N-type calcium channels which control neurotransmission at many synapses. Macrocyclic peptide compounds have also shown considerable promise in a wide range of other therapeutic areas and have yielded several clinically approved therapeutics for cancer, immunomodulation (e.g. cyclosporin A), and fungal infections (e.g. echinocandins).
The utility and fields of application of these compounds are often limited by the low yields of their extraction from their natural sources, challenges in their organic synthesis, and the inability to source large numbers of variants to optimize activity. For this reason, biotechnological or semisynthetic approaches beginning with natural starting materials are often utilized for drug manufacture. A particularly exciting group of macrocyclic peptides are the multiply backbone N-methylated cyclic peptides (cyclic peptides that are N-methylated at multiple locations on the peptide backbone). These compounds have interesting pharmacological properties, e.g. increased bioavailability due to increased permeability through intestinal epithelial membranes, and increased half-life in vivo due to increased stability towards proteases. The prototypical representative of this family of peptides is the immunomodulator Cyclosporin A. Cyclosporin A is an 11-mer cyclic peptide that was originally isolated from the ascomycete Tolypocladium inflatum, which synthesizes Cyclosporin A via a highly complex non-ribosomal peptide synthetase (NRPS) specifically referred to as cyclosporin synthase. The backbone methylation of cyclosporin occurs during the elongation of the peptide via built-in methyltransferase domains within cyclosporin synthase. Many teams over the past couple of decades have attempted to re-engineer or evolve the NRPS machinery in order to produce altered versions or diversified derivatives of their natural product (e.g. different amino acids, different size cycle, different N-methylation patterns, etc.), but these efforts have proven to be disappointingly unfruitful and challenging.
The currently established methods for producing these types of multiply N-methylated cyclic peptides involve the fermentation of large cultures of the corresponding microorganisms that naturally produce these compounds followed by elaborate fractionation and purification methods. A few alternatives have been established for a handful of compounds that either rely on a total chemical synthesis or a mixed enzymological and semi-synthetic hybrid strategy.
Ribosomally synthesized and post-translationally modified peptides (RiPPs) are a diverse class of natural products of ribosomal origin consisting of more than 22 subclasses that are produced by a variety of organisms, including bacteria, eukaryotes, and archaea. RiPPs are typically produced as an all-L pro-protein that is encoded on a gene that is transcribed by the regular RNA Polymerase II machinery (in eukaryotes) and then translated by the ribosome. The active macrocycle is encoded within a cassette that is flanked by N- and C-terminal signal recognition motifs. After its translation, the all-L pro-protein is processed by a set of modifying enzymes that introduce several modifications (e.g. side chain acylation, isomerization of some or all positions from L- to D-amino acids, side chain hydroxylation, backbone N-methylation, end-to-end cyclization, disulfide bridge formation, tryptathionine bridge formation, and many others) that liberate the cassette peptide out of the pro-protein and then convert it into the final natural product. The N- and C-terminal signal recognition motifs act as docking sites for the processing enzymes and guide the order and kinetics of catalysis.
One of the recurrent features about RiPP processing enzymes is that many of them are virtually completely agnostic to the sequence of the encoded active peptide within the cassette, thereby affording a high tolerability of substitutions in the cassette. Studies on the Amatoxin/Phallatoxin/MSDin family of poisonous mushroom RiPPs confirm the notion of the promiscuity of the corresponding prolyloligopeptidase/macrocyclase, PopB, towards a variety of naturally occurring active peptide cassette sequence variants as well as towards many synthetically derived variants. Such findings present the possibility for a straightforward strategy to generate widely diversified derivatives of a RiPP-based natural product by simply altering the DNA of the cassette coding sequence within the pro-protein encoding gene.
Disclosed herein are methods for identifying one or more molecules that elicit degradation of a first test protein in a host cell. The method may comprise expressing in the host cell (i) an E3 ubiquitin ligase or a functional fragment thereof; (ii) a first fusion protein comprising a first DNA-binding moiety, the first test protein, and a first gene-activating moiety. The host cell may comprise a promoter sequence for controlling expression of a death agent wherein the first DNA-binding moiety specifically binds to the promoter sequence. The molecule may be delivered to the host cell. In the absence of the molecule, expression of the death agent may be activated. In the presence of the molecule, the first test protein may be degraded by the E3 ubiquitin ligase.
In some embodiments, the method further comprises expressing a second fusion protein comprising a second DNA-binding moiety, a second test protein, and a second gene-activating moiety in the host cell, wherein the host cell further may comprise one or more positive selection reporters driven by one or more promoters with a sequence specific for the second DNA-binding moiety.
In some embodiments, the method further comprises a plurality of positive selection reporters which are disposed within the host cell, wherein each positive selection reporter of the plurality of positive selection reporters is operably linked to a promoter sequence specific for the second DNA-binding moiety. In some embodiments, the positive selection reporter(s) are encoded in a plasmid disposed within the host cell.
In some embodiments, the molecule may be part of a library of molecules. In some embodiments, the molecule from the library may be delivered exogenously. In some embodiments, the molecule may be produced within the cell. In some embodiments, the molecule may be produced within the cell from a DNA encoded library.
In some embodiments, methods for identifying a molecule that selectively mediates the degradation of a specific test protein in a host cell while preserving a second test protein are described. The methods may comprise: expressing in the host cell a first fusion protein comprising the test protein with an activation domain and a DNA-binding moiety; a second test protein with an activation domain and a DNA-binding moiety; expressing in the host cell a third protein comprising an E3 ligase along with the required ubiquitination machinery components; and delivering a molecule from a library to the host cell, wherein a sequence of a gene for expressing a negative selection death agent is disposed within the host cell and operably linked to a promoter DNA sequence specific for the DNA binding moiety of the first fusion protein, wherein a positive selection reporter is disposed within the host and operably linked to a promoter DNA sequence specific for the DNA binding moiety of the second fusion protein and wherein, in the absence of the molecule, the expression of the first test protein causes the gene activating moiety to activate expression of the death agent, while the expression of the second test protein causes the gene activating moiety to activate the expression of the positive selection reporter.
In some embodiments, the molecule from the library is delivered exogenously. In some embodiments, the molecule is produced within the cell. In some embodiments, the molecule is produced within the cell from a DNA encoded library. In some embodiments, the host cell comprises more than one sequence for expressing a positive control reporter that is activated by a promoter DNA sequence specific for a DNA binding moiety. In some embodiments, the host cell comprises more than one sequence for expressing a death agent that is activated by a promoter DNA sequence specific for a DNA binding moiety. In some embodiments, the host cell comprises an integrated DNA encoding the first fusion protein, an integrated DNA encoding the second fusion protein, an integrated DNA encoding the third fusion protein; a plasmid DNA encoding the death agent; and a plasmid DNA encoding a positive selection reporter.
In some embodiments, the first test protein is a variation of KRAS. In some embodiments, the second test protein is KRAS. In some embodiments, the first test protein is androgen receptor splice variants ARV (ARV3, ARV7, or ARV9). In some embodiments, the second test protein is wild-type androgen receptor. In some embodiments, the first test protein is a variation of IDH. In some embodiments, the second test protein is wild-type IDH. In some embodiments, the first test protein is Myc. In some embodiments, the first test protein is CCNE. In some embodiments, the first test protein is Estrogen Receptor (ER). In some embodiments, the first test protein is IKZF1 or IKZF2. In some embodiments, the first test protein is PD-1 or PDL-1. In some embodiments, the first test protein is CTLA-4. In some embodiments, the first test protein is Tau. In some embodiments the first test protein is Act1/CIKS (Connection to IκB Kinase and Stress-activated protein kinases). In some embodiments the first test protein is an Ets Transcription factor variant (ETV1, ETV2, ETV3, ETV4, or ETV5). In some embodiments, the DNA binding moiety is derived from LexA, cI, Gli-1, YY1, Glucocorticoid receptor, TetR, or Ume6. In some embodiments, the gene activating moiety is derived from VP16, GAL4, NF-κB, B42, BP64, VP64, or p65.
In some embodiments, the death agent is an overexpressed product of genetic element selected from DNA or RNA. In some embodiments, the genetic element is a Growth Inhibitory (GIN) sequence such as GIN11. In some embodiments, the death agent is a ribosomally encoded xenobiotic agent, a ribosomally encoded poison, a ribosomally encoded endogenous or exogenous gene that results in severe growth defects upon mild overexpression, a ribosomally encoded recombinase that excises an essential gene for viability, a limiting factor involved in the synthesis of a toxic secondary metabolite, or any combination thereof. In some embodiments, the death agent is Cholera toxin, SpvB toxin, CARDS toxin, SpyA Toxin, HopUl, Chelt toxin, Certhrax toxin, EFV toxin, ExoT, CdtB, Diphtheria toxin, ExoU/VipB, HopPtoE, HopPtoF, HopPtoG, VopF, YopJ, AvrPtoB, SdbA, SidG, VpdA, Lpg0969, Lpg1978, YopE, SptP, SopE2, SopB/SigD, SipA, YpkA, YopM, Amatoxin, Phallacidin, Killer toxin KP1, Killer toxin KP6, Killer Toxin K1, Killer Toxin K28 (KHR), Killer Toxin K28 (KHS), Anthrax lethal factor endopeptidase, Shiga Toxin, Saporin Toxin, Ricin Toxin, or any combination thereof.
In some embodiments, the host cell is a fungus or bacteria. In some embodiments, the fungus is Aspergillus. In some embodiments, the fungus is Pichia pastoris. In some embodiments, the fungus is Komagataella phaffii. In some embodiments, the fungus is Ustilago maydis. In some embodiments, the fungus is Saccharomyces cerevisiae.
In some embodiments, the molecule is small molecule. In some embodiments, the small molecule is peptidomimetic. In some embodiments, the molecule is peptide or protein. In some embodiments, the peptide or protein is derived from naturally occurring protein product. In certain embodiments, the peptide or protein is synthesized protein product. In some embodiments, the peptide or protein is product of recombinant genes. In some embodiments, the molecule is a peptide or protein expressed from test DNA molecule inserted into the host cell, wherein the test DNA molecule comprises DNA sequences that encodes polypeptides, forming the library. In some embodiments, the library comprises polypeptides 60 or fewer amino acids in length. In some embodiments, the DNA sequence encodes a 3′UTR of mRNA. In some embodiments, the 3′UTR is the 3′UTR of sORF1. In some embodiments, the polypeptides comprise a common N-terminal sequence of Methionine-Valine-Asparagine. In some embodiments, the polypeptides in the library are processed into cyclic or bicyclic peptides in the host cell.
Disclosed herein, in certain embodiments, is a plasmid vector. In some embodiments, the plasmid vector comprises a DNA sequence encoding a first polypeptide inserted in frame with Gal4-DNA binding domain (“DBD”) and VP16 activation domain (AD), a DNA sequence encoding a second polypeptide inserted in frame with Ume6-DNA binding domain (“DBD”) and VP16 activation domain (AD), and a DNA sequence encoding a third polypeptide. In certain embodiments, a host cell comprises the plasmid vectors.
Disclosed herein, in certain embodiments, is a library of plasmid vectors, each plasmid vector comprising: a DNA sequence encoding a different peptide sequence operably linked to a first switchable promoter; a DNA sequence encoding a death agent under control of a second switchable promoter; and a DNA sequence encoding a positive selection reporter under control of a third switchable promoter. In some embodiments, the different peptide sequence encodes a common N-terminal stabilization sequence. In some embodiments, the DNA sequence encodes a mRNA sequence comprising a 3′UTR. In some embodiments, the different peptide sequence is 60 amino acids or fewer in length. In some embodiments, the different peptide sequences are random. In some embodiments, the different peptide sequences are pre-enriched for binding to a target. In some embodiments is a library of host cells, each comprises a library of the plasmid vectors.
Disclosed herein, in certain embodiments, is a library of plasmid vectors, each plasmid vector comprising: a DNA sequence encoding a peptide N-methyltransferase operably linked to a first switchable promoter; a prolyloligopeptidase operably linked to a second switchable promoter; In some embodiments, the different peptide sequence is 18 amino acids or fewer in length. In some embodiments, the different peptide sequences are random. In some embodiments, the different peptide sequences are pre-enriched for binding to a target. In some embodiments is a library of host cells, each comprises a library of the plasmid vectors.
Described herein is a host cell configured to accelerate the degradation of a specific protein. The host cell may express an E3 ubiquitin ligase or a functional fragment thereof; a first fusion protein comprising a first test protein, a first DNA-binding moiety, and a first gene-activating moiety; a death agent, wherein the expression of the death agent is under control of a promoter DNA sequence specific for the first DNA-binding moiety; and a polypeptide of 60 or fewer amino acids, wherein the polypeptide modulates an interaction between the first fusion protein and the E3 ubiquitin ligase in a manner that leads to accelerated degradation of the first fusion protein.
In some embodiments, the host cell further comprises a second fusion protein comprising a second DNA-binding moiety, a second test protein, and a second gene-activation moiety; and a positive selection reporter, wherein the expression of the positive reporter is under control of a second promoter DNA sequence specific for the second DNA-binding moiety.
In some embodiments, the polypeptide encodes an N-terminal sequence for peptide stabilization. In some embodiments, the polypeptide is a macrocycle. In some embodiments, the polypeptide is an N-methylated macrocycle. In some embodiments, the polypeptide is an encoded product of an mRNA, wherein the mRNA comprises a 3′UTR. In some embodiments, the mRNA is an encoded product of a DNA molecule, wherein the DNA molecule is delivered into the host cell exogenously. In some embodiments, synthetic compound libraries can be tested.
In some embodiments, the host cell is a eukaryote or a prokaryote. In some embodiments, the host cell is animal, plant, a fungus, or bacteria. In some embodiments, the host cell is a haploid yeast cell. In some embodiments, the host cell is a diploid yeast cell. In some embodiments, the diploid yeast cell is produced by mating a first host cell comprising DNA sequences encoding the first chimeric gene, the second chimeric gene, and the third chimeric gene, to a second host cell comprising DNA sequences encoding the death agent, positive selection reporter, and the mRNA comprising a nucleotide sequence encoding a polypeptide. In some embodiments, the fungus is Aspergillus. In some embodiments, the fungus is Pichia pastoris. In some embodiments, the fungus is Komagataella phaffii. In some embodiments, the fungus is Ustilago maydis.
Disclosed herein are kits for accelerated degradation of selective target proteins. A kit may comprise a first plasmid vector encoding a first fusion protein comprising a first test protein that may be inserted in frame between a first DNA-binding moiety and an activating domain; a second fusion protein that may be inserted in frame between a second DNA-binding moiety and a second activating domain; and the library of plasmid vectors mentioned above.
In some embodiments, the kit further comprises a second plasmid vector configured for expressing an E3 ligase within a host cell. In some embodiments, the first vector may encode an E3 ubiquitin ligase.
Disclosed herein are methods for identifying one or more molecules that elicit degradation of a first test protein. The methods may comprise expressing in a plurality of host cells: (i) an E3 ubiquitin ligase or a functional fragment thereof; and (ii) a first fusion protein comprising a first DNA-binding moiety, the first test protein, and a first gene-activating moiety. The plurality of host cells may each comprise a promoter sequence for controlling expression of a death agent and the first DNA-binding moiety may specifically bind to the promoter sequence such that expression of the death agent is activated in the absence of a molecule that recruits the E3 ubiquitin ligase to the first fusion protein in a manner that results in ubiquitination and premature degradation of the first fusion protein. The method may comprise delivering a different molecule to each of the plurality of host cells and identifying a molecule that elicits degradation of the first test protein based on survival of a cell into which the molecule was delivered.
Disclosed herein, in certain embodiments, is a method for identifying a molecule that selectively facilitates an interaction between a first test protein and a second test protein leading to its degradation, comprising: expressing in the host cell a first fusion protein comprising the first test protein and a DNA-binding moiety and a gene activating moiety; expressing in the host cell a second fusion protein comprising the second test protein a DNA-binding moiety and a gene activating moiety; expressing in the host cell a third protein comprising an E3 ubiquitin ligase; and delivering a molecule from a library to the host cell such that the molecule forms a bridging interaction between the first test protein and the E3 ubiquitin ligase, leading to its selective degradation; wherein a sequence of a gene for expressing a death agent is disposed within the host cell and operably linked a promoter DNA sequence specific for the DNA binding moiety of the first fusion protein; wherein a positive selection reporter is disposed within the host cell and operably linked to a promoter DNA sequence specific for the DNA binding moiety of the second fusion protein. The first test protein may form a functional transcription factor that activates expression of the death agent; and the second test protein may form a functional transcription factor that activates expression of a positive selection reporter.
In some embodiments, the host cell comprises more than one sequence for expressing a death agent that is activated by the promoter DNA sequence specific for a DNA binding moiety. In some embodiments, the host cell comprises more than one sequence for expressing a positive control reporter that is activated by a promoter DNA sequence specific for a DNA binding moiety.
In some embodiments, the host cell comprises an integrated DNA encoding the first fusion protein, an integrated DNA encoding the second fusion protein, an integrated DNA encoding the third fusion protein; a plasmid DNA encoding the death agent; and a plasmid DNA encoding a positive selection reporter.
In some embodiments, the DNA binding moiety is derived from LexA, cI, Gli-1, YY1, Glucocorticoid receptor, TetR, or Ume6. In some embodiments, the gene activating moiety is derived from VP16, Gal4, NF-κB, B42, BP64, VP64, or p65. In some embodiments, the death agent is a genetic element wherein overexpression of genetic material results in growth inhibition of the host cell. In some embodiments, the death agent is an overexpressed product of DNA. In some embodiments, the death agent is an overexpressed product of RNA. In some embodiments, the sequence of the gene for expressing the death agent is a Growth Inhibitory (GIN) sequence such as GIN11. In some embodiments, the death agent is a ribosomally encoded xenobiotic agent, a ribosomally-encoded poison, a ribosomally-encoded endogenous or exogenous gene that results in severe growth defects upon mild overexpression, a ribosomally-encoded recombinase that excises an essential gene for viability, a limiting factor involved in the synthesis of a toxic secondary metabolite, or any combination thereof. In some embodiments, the death agent is Cholera toxin, SpvB toxin, CARDS toxin, SpyA Toxin, HopUl, Chelt toxin, Certhrax toxin, EFV toxin, ExoT, CdtB, Diphtheria toxin, ExoU/VipB, HopPtoE, HopPtoF, HopPtoG, VopF, YopJ, AvrPtoB, SdbA, SidG, VpdA, Lpg0969, Lpg1978, YopE, SptP, SopE2, SopB/SigD, SipA, YpkA, YopM, Amatoxin, Phallacidin, Killer toxin KP1, Killer toxin KP6, Killer Toxin K1, Killer Toxin K28 (KHR), Killer Toxin K28 (KHS), Anthrax lethal factor endopeptidase, Shiga Toxin, Saporin Toxin, Ricin Toxin, or any combination thereof.
In some embodiments, the first test protein is a variation of KRAS. In some embodiments, the second test protein is KRAS. In some embodiments, the first test protein is androgen receptor splice variants ARV (ARV3, ARV7, or ARV9). In some embodiments, the second test protein is wild-type androgen receptor. In some embodiments, the first test protein is a variation of IDH. In some embodiments, the second test protein is wild-type IDH. In some embodiments, the first test protein is Myc. In some embodiments, the first test protein is CCNE. In some embodiments, the first test protein is Estrogen Receptor (ER). In some embodiments, the first test protein is IKZF1 or IKZF2. In some embodiments, the first test protein is PD-1 or PDL-1. In some embodiments, the first test protein is CTLA-4. In some embodiments, the first test protein is Tau. In some embodiments the first test protein is Act1/CIKS (Connection to IκB Kinase and Stress-activated protein kinases). In some embodiments the first test protein is an Ets Transcription factor variant (ETV1, ETV2, ETV3, ETV4, or ETV5).
In some embodiments, the molecule is small molecule. In some embodiments, the small molecule is peptidomimetic. In some embodiments, the molecule is peptide or protein. In some embodiments, the peptide or protein is derived from naturally occurring protein product. In some embodiments, the peptide or protein is synthesized protein product. In some embodiments, the peptide or protein is product of recombinant genes. In some embodiments, the peptide or protein is expressed product of test DNA molecule inserted into the host cell, wherein the test DNA molecule comprises of DNA sequences that encodes polypeptides, forming the library. In some embodiments, the library comprises of sixty or fewer amino acids.
In some embodiments, the peptide or protein is a product of post-translational modification. In some embodiments, the post-translational modification includes cleavage. In some embodiments, the post-translational modification includes cyclization. In some embodiments, the post-translational modification includes bi-cyclization. In some embodiments, the cyclization comprises reacting with prolyl endopeptidase. In some cases, the prolyl endopeptidase may be one selected from SEQ ID NOs: 42-58 or functional fragments thereof. In some cases, the prolyl endopeptidase may be one with at least 80%, 85%, 90%, 92%, 95%, 97% or 99% sequence identity to one of SEQ ID NOs: 42-58.
In some embodiments, the cyclization comprises reacting with beta-lactamase. In some cases, the lactamase may be one selected from SEQ ID NOs: 119-120 or functional fragments thereof. In some cases, the lactamase may be one with at least 80%, 85%, 90%, 92%, 95%, 97% or 99% sequence identity to one of SEQ ID NOs: 119-120.
In some embodiments, the bicyclization comprises reacting with hydroxylase and dehydratase. In some cases, the hydroxylase may comprise SEQ ID NO: 123 or functional fragments thereof. In some cases, the hydroxylase may be one with at least 80%, 85%, 90%, 92%, 95%, 97% or 99% sequence identity to SEQ ID NO: 123. In some cases, the dehydratase may be one selected from SEQ ID NOs: 124-127 or functional fragments thereof. In some cases, the dehydratase may be one with at least 80%, 85%, 90%, 92%, 95%, 97% or 99% sequence identity to one of SEQ ID NOs: 124-127.
In some embodiments, the bicyclization is formed by a tryptathionine bridge. In some embodiments, the post-translational modification includes methylation. In some embodiments, the methylation comprises reacting with N-methyltransferase. In some cases, the N-methyltransferase is one selected from SEQ ID NOs: 61-116 or functional fragments thereof. In some cases, the N-methyltransferase may be one with at least 80%, 85%, 90%, 92%, 95%, 97% or 99% sequence identity to one of SEQ ID NOs: 61-116. In some embodiments, the post-translational modification includes halogenation. In some embodiments, the post-translational modification includes glycosylation. In some embodiments, the post-translational modification includes acylation. In some embodiments, the post-translational modification includes phosphorylation. In some embodiments, the post-translational modification includes acetylation.
In some embodiments, the test DNA molecule comprises of gene sequence expressing modifying enzyme. In some embodiments, the test DNA molecule comprises of a gene sequence expressing N-terminal sequence of methionine-valine-asparagine. In some embodiments, the test DNA molecule comprises of a gene sequence encoding a 3′UTR. In some embodiments, the 3′UTR is 3′UTR of sORF1.
In some embodiments, the host cell is a eukaryote or a prokaryote. In some embodiments, the host cell is animal, plant, a fungus, or bacteria. In some embodiments, the fungus is Aspergillus. In some embodiments, the fungus is Pichia pastoris. In some embodiments, the fungus is Komagataella phaffii. In some embodiments, the fungus is Ustilago maydis.
Disclosed herein are compositions and methods comprising genes and peptides associated with cyclic and backbone-methylated macrocyclic peptides and macrocyclic peptide production in a cell. In particular, the present invention relates to using genes and proteins from Gymnopus species encoding peptides specifically relating to gymnopeptides in addition to proteins involved with processing of such types of cyclic peptides. In a preferred embodiment, the present invention also relates to methods for making small peptides and small cyclic peptides including peptides like gymnopeptides through heterologous expression in a eukaryotic, prokaryotic, or cell free system.
The methods further describe the uses of the enzymes heterologously to produce libraries of macrocycles, with possible N-terminal methylation events, inside a host cell to enable screening for functional molecules. In some instances, the functional molecules can modulate the interaction of two proteins, either to disrupt or bridge a protein-protein interaction. Also described is selection of modified macrocycles that are able to bridge an interaction between an E3 ubiquitin ligase and a protein, leading to functional degradation of the protein.
In some embodiments, described herein are methods of producing cyclic peptides. The method for producing cyclic peptides may comprise recombinantly expressing a prolyloligopeptidase; and contacting the prolyloligopeptidase with a linear peptide such that the linear peptide is converted to a cyclic peptide; wherein the active site of prolyloligopeptidase does not have a tryptophan residue at a position corresponding to amino acid position 603 of SEQ ID NO: 55, and/or an asparagine residue at a position corresponding to amino acid 563 of SEQ ID NO: 55.
In some embodiments, the prolyloligopeptidase has a leucine at amino acid position 603 corresponding to amino acid position 603 of SEQ ID NO: 55, and/or a serine residue at amino acid position 563 corresponding to amino acid position 563 of SEQ ID NO:55. In some embodiments, the prolyoligopeptidase comprises a sequence corresponding to any one of SEQ ID NOs: 42-58. In some embodiments, the prolyoligopeptidase is one with at least 80%, 85%, 90%, 92%, 95%, 97% or 99% sequence identity to one of SEQ ID NOs: 42-58.
In some embodiments, contacting the prolyloligopeptidase with the linear peptide occurs within a cell. In some embodiments, contacting the prolyloligopeptidase with the linear peptide does not occur within a cell. In some embodiments, the linear peptide is recombinantly expressed. In some embodiments, the cyclic peptide comprises 18 or more amino acids.
In some embodiments, described herein are methods of identifying a cyclic peptide which disrupts an interaction between a first test protein and a second test protein. The method may comprise: (a) expressing in the host cell: (i) a first fusion protein comprising a first DNA-binding moiety, the first test protein, and a first gene-activating moiety; and (ii) a second test protein; and (b) delivering the peptide to the host cell; wherein, in the absence of the cyclic peptide, expression of a death agent is activated.
In some embodiments, described herein are methods of identifying a cyclic peptide which bridges an interaction between a first test protein and a second test protein. The method may comprising: (a) expressing in the host cell: (i) a first fusion protein comprising a first DNA-binding moiety, the first test protein, and a first gene-activating moiety; and (ii) a second test protein; and (b) delivering the peptide to the host cell; wherein, in the absence of the cyclic peptide, expression of a death agent is activated.
In some embodiments, described herein are methods of methylating a peptide. The method may comprise: recombinantly expressing an N-methyl transferase; and contacting the N-methyltransferase with a peptide such that a plurality of nitrogens in the backbone of the peptide are methylated; wherein N-methyl transferase comprises the sequence of one of SEQ ID NOs: 61-116.
In some embodiments, the contacted peptide is a cyclic peptide. In some embodiments, the peptide or cyclic peptide comprises 18 or more amino acids. In some embodiments, contacting the N-methyltransferase with the peptide occurs within a cell. In some embodiments, contacting the N-methyltransferase with the peptide does not occur within a cell. In some embodiments, the peptide is recombinantly expressed.
In some embodiments, described herein are methods for identifying a cyclic peptide that disrupts an interaction between a first test protein and a second test protein. The method may comprise: (a) expressing in the host cell: (i) a first fusion protein comprising a first DNA-binding moiety, the first test protein, and a first gene-activating moiety; and (ii) a second test protein; and (b) delivering the peptide to the host cell; wherein, in the absence of the cyclic peptide, expression of a death agent is activated.
In some embodiments, described herein are methods for identifying a cyclic peptide that bridges an interaction between a first test protein and a second test protein. The method may comprise: (a) expressing in the host cell: (i) a first fusion protein comprising a first DNA-binding moiety, the first test protein, and a first gene-activating moiety; and (ii) a second test protein; and (b) delivering the peptide to the host cell; wherein, in the absence of the cyclic peptide, expression of a death agent is activated.
All publications, patents, and patent applications mentioned in this specification are herein incorporated by reference to the same extent as if each individual publication, patent, or patent application was specifically and individually indicated to be incorporated by reference.
Features of the 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 embodiments, in which the principles of the disclosure are utilized, and the accompanying drawings of which:
The present disclosure provides a system that can use a unified eukaryotic or prokaryotic one-hybrid system in which a bait expression plasmid is used in both organismal contexts. Additionally, an extensive series of leucine zipper fusion proteins of known affinities can be generated to compare the efficiency of interaction detection using such systems. The yeast system can produce a quantitative readout over a dynamic range. In addition, modified expression vectors disclosed herein can be used for expression of a protein of interest in both eukaryotes and prokaryotes.
The present disclosure also provides a system for delivering molecules across the cell membrane. The cell membrane presents a major challenge in drug discovery, especially for biologics such as peptides, proteins, and nucleic acids. One potential strategy to subvert the membrane barrier and deliver biologics into cells is to attach them to “cell penetrating peptides” (CPPs). Despite three decades of investigation, the fundamental basis for CPP activity remains elusive. CPPs that enter cells via endocytosis generally exit from endocytic vesicles in order to reach the cytosol. Unfortunately, the endosomal membrane has proven to be a significant barrier towards cytoplasmic delivery of these CPPs such that often a negligible fraction of the peptides escapes into the cell interior. What are thus needed are new scaffolds and structures that impart peptides with highly proficient intrinsic cell penetrating ability to various cell types. Several naturally occurring polyketides and peptides exhibit remarkable cell permeability (e.g. cyclosporine and amanitins). These peptides are characterized by specific modifications (e.g., N-methylation of the backbone and cyclization or bicyclization) that can play a crucial role in their cell membrane permeability. The compositions and methods disclosed herein describe methods and approaches that enable the general utilization of similar modifications to generate compositions that may be of high therapeutic value and that may be capable of degrading proteins with high selectivity.
Definitions
As used herein, “reporter gene” refers to a gene whose expression can be assayed. Such genes include, for example, LacZ, β-glucuronidase (GUS), amino acid biosynthetic genes, the yeast LEU2, HIS3, LYS2, or URA3 genes, nucleic acid biosynthetic genes, the mammalian chloramphenicol transacetylase (CAT) gene, the green fluorescent protein (GFP) or any surface antigen gene for which specific antibodies are available. Reporter genes can result in both positive and negative selection.
An “allele” refers to a DNA sequence of a gene which includes a naturally occurring, or pathogenic variant of a gene. Expression of differing alleles may lead to different protein variants.
A “promoter” is a DNA sequence located proximal to the start of transcription at the 5′ end of an operably linked transcribed sequence. The promoter can contain one or more regulatory elements or modules, which interact in modulating transcription of the operably linked gene. Promoters can be switchable or constitutive. Switchable promoters allow for reversible induction or repression of operably linked target genes upon administration of an agent. Examples of switchable promoters include but are not limited to the LexA operator and the alcohol dehydrogenase I (alcA) gene promoter. Examples of constitutive promoters include the human beta-actin gene promoter.
“Operably linked” describes two macromolecular elements arranged such that modulating the activity of the first element induces an effect on the second element. In this manner, modulation of the activity of a promoter element can be used to alter or regulate the expression of an operably-linked coding sequence. For example, the transcription of a coding sequence that is operably-linked to a promoter element can be induced by factors that activate the promoter's activity; transcription of a coding sequence that is operably-linked to a promoter element can be inhibited by factors that repress the promoter's activity. Thus, a promoter region is operably-linked to the coding sequence of a protein if transcription of such coding sequence activity is influenced by the activity of the promoter.
“In frame” as used herein throughout, refers to the proper positioning of a desired sequence of nucleotides within a DNA fragment or coding sequence operably linked to a promoter sequence, thereby permitting transcription and/or translation.
“Fusion construct” refers to recombinant genes that encode fusion proteins.
A “fusion protein” is a hybrid protein, i.e., a protein that has been constructed to contain domains from at least two different proteins. Fusion proteins described herein can be a hybrid proteins that possess both (1) a transcriptional regulatory domain from a transcriptional regulatory protein or a DNA binding domain from a DNA binding protein and (2) a heterologous protein to be assayed for interaction status. The protein that is the source of the transcriptional regulatory domain may different from the protein that is the source of the DNA binding domain. In other words, the two domains may be heterologous to each other.
A transcriptional regulatory domain of a bait fusion protein can either activate or repress transcription of target genes, depending on the biological activity of the domain. Bait proteins of the disclosure may also be part of a fusion protein where a protein of interest is operably linked to a DNA binding moiety and a transcriptional activation domain.
“Bridging interaction” refers to an interaction between a first protein and a second that occurs only when one or both of the first protein and the second protein interact with a molecule, such as a peptide or small molecule from a library. In some cases, the bridging interaction between the first protein and the second protein is direct, while in other cases the bridging interaction between the first protein and the second protein is indirect. In some cases, the interaction leads to an activity of one protein being exerted on a second protein, such as ubiquitination and subsequent degradation.
“Expression” is the process by which the information encoded within a gene is revealed. If the gene encodes a protein, then expression involves both transcription of the DNA into mRNA, the processing of mRNA (if necessary) into a mature mRNA product, and translation of the mature mRNA into protein.
As used herein, a “cloning vehicle” is any entity that is capable of delivering a nucleic acid sequence into a host cell for cloning purposes. Examples of cloning vehicles include plasmids or phage genomes. A plasmid that can replicate autonomously in the host cell is especially desired. Alternatively, a nucleic acid molecule that can insert (integrate) into the host cell's chromosomal DNA is useful, especially a molecule that inserts into the host cell's chromosomal DNA in a stable manner, that is, a manner that allows such molecule to be inherited by daughter cells.
Cloning vehicles are often characterized by one or a small number of endonuclease recognition sites at which such DNA sequences may be cut in a determinable fashion without loss of an essential biological function of the vehicle, and into which DNA may be spliced in order to bring about its replication and cloning.
The cloning vehicle can further contain a marker suitable for use in the identification of cells transformed with the cloning vehicle. For example, a marker gene can be a gene that confers resistance to a specific antibiotic on a host cell.
The word “vector” can be used interchangeably with “cloning vehicle.”
As used herein, an “expression vehicle” is a vehicle or vector similar to the cloning vehicle that is especially designed to provide an environment that allows the expression of the cloned gene after transformation into the host. One manner of providing such an environment is to include transcriptional and translational regulatory sequences on such expression vehicles, such transcriptional and translational regulatory sequences being capable of being operably linked to the cloned gene. Another manner of providing such an environment is to provide a cloning site or sites on such vehicle, wherein a desired cloned gene and a desired expression regulatory element can be cloned.
In an expression vehicle, the gene to be cloned is usually operably-linked to certain control sequences such as promoter sequences. Expression control sequences will vary depending on whether the vector is designed to express the operably-linked gene in a prokaryotic or eukaryotic host and can additionally contain transcriptional elements such as enhancer elements, termination sequences, tissue-specificity elements, or translational initiation and termination sites.
A “host” refers to any organism that is the recipient of a cloning or expression vehicle. The host may be a bacterial cell, a yeast cell or a cultured animal cell such as a mammalian or insect cell. The yeast host may be Saccharomyces cerevisiae.
A “host cell” as described herein can be a bacterial, fungal, or mammalian cell or from an insect or plant. Examples of bacterial host cells are E. coli and B. subtilis. Examples of fungal cells are S. cerevisiae and S. pombe. Non-limiting examples of mammalian cells are immortalized mammalian cell lines, such as HEK293, A549, HeLa, or CHO cells, or isolated patient primary tissue cells that have been genetically immortalized (such as by transfection with hTERT). Non-limiting example of the plant is Nicotiana tabacum or Physcomitrella patens. A non-limiting example of insect cell is a sf9 (Spodoptera frugiperda) cell.
A “DNA-binding domain (DBD),” or a “DNA-binding moiety” is a moiety that is capable of directing specific polypeptide binding to a particular DNA sequence (i.e., a “protein binding site”). These proteins can be homodimers or monomers that bind DNA in a sequence specific manner. Exemplary DNA-binding domains of the disclosure include LexA, cI, glucocorticoid receptor binding domains, and the Ume6 domain.
A “gene activating moiety” or “activation domain” (“AD”) is a moiety that is capable of inducing (albeit in many instances weakly inducing) the expression of a gene to whose control region it is bound (one example is an activation domain from a transcription factor). As used herein, “weakly” is meant below the level of activation effected by GAL4 activation region II and is preferably at or below the level of activation effected by the B42 activation domain. Levels of activation can be measured using any downstream reporter gene system and comparing, in parallel assays, the level of expression stimulated by the GAL4 region II-polypeptide with the level of expression stimulated by the polypeptide to be tested.
The term “sequence identity” as used herein in the context of amino acid sequences is defined as the percentage of amino acid residues in a candidate sequence that are identical with the amino acid residues in a selected sequence, after aligning the sequences and introducing gaps, if necessary, to achieve the maximum percent sequence identity, and not considering any conservative substitutions as part of the sequence identity. Alignment for purposes of determining percent amino acid sequence identity can be achieved in various ways that are within the skill in the art, for instance, using publicly available computer software such as BLAST, BLAST-2, ALIGN, ALIGN-2 or Megalign (DNASTAR) software. Those skilled in the art can determine appropriate parameters for measuring alignment, including any algorithms needed to achieve maximal alignment over the full-length of the sequences being compared.
Screening for Functional Degraders of a Target Protein
Selective protein degradation is a unique approach to drug discovery. The ability to selectively degrade an aberrant protein or its isoform poses a controlled approach to selectively target certain pathologies such as cancer. Compounds that accomplish selective degradation through bridging to E3 ubiquitin ligases are catalytic in nature, and are not required in stoichiometric levels, making them lucrative drug compounds. Screening for compounds that selectively bridge a protein of interest to an E3 ubiquitin ligase doesn't always guarantee a functional degradation of the target protein in question. Screening for compounds that are able to functionally degrade a target protein by forming a transient tertiary complex between itself, the target, and an E3 ligase is difficult to perform. Current screens rely on identifying compounds specific to the target and chemically linking them to anther moiety that binds to a specific E3 ligase, creating large molecules that are limited to targets with known small molecule binders.
Methods and systems of the disclosure can involve the intracellular selection of peptide based selective degraders. Stated differently, various systems described herein can be used to screen for molecules that selectively lead to the degradation of a target protein by creating a functional interaction between the target protein and an E3 ubiquitin ligase or directly to the proteasome. A model organism, for example Saccharomyces cerevisiae, can be employed, for the coexpression of a target of interest with a specific E3 ubiquitin ligase and a test DNA molecule comprising a DNA sequence that encodes a randomized peptide library. This can allow for the selection of unbiased peptides that lead to a functional degradation of the target of interest using selection mechanisms (e.g., stringent viability readout selection mechanisms). The method can involve a permutation of a yeast one-hybrid system that can rely on the degradation of a transcription factor that requires an interaction between the test protein fused to a DNA binding domain (DBD) and transcription activation domain (AD) by the proteasome or through a specific E3 ubiquitin ligase via a peptide-mediated interaction (see
Methods and systems of the disclosure can use the reconstitution of a transcription factor mediated by a test protein fused to an AD, for example, VP16, NF-κB AD, VP64AD, BP64 AD, B42 acidic activation domain (B42AD), or p65 transactivation domain (p65AD) and a DBD, for example, LexA, cI, Gli-1, YY1, glucocorticoid receptor binding domain, or Ume6 domain. Similarly, the test protein can comprise an AD and bind to DNA through another binding partner.
Methods and system of the disclosure can also use two different proteins, or two variants of one protein, fused to different DBDs and ADs. The system can identify compounds that bridge one of the proteins to an E3 ligase leading to its degradation, while preserving an active version of the other test protein. For example, degrading one component in a complex without affecting the rest of the complex integrity (see
Expression of the protein of interest can direct RNA polymerase to a specific genomic site and allow for the expression of a genetic element. The genetic element can be, for example, a gene that encodes a protein that enables an organism to grow on selection media. The selection media can be specific to, for example, ADE2, URA3, TRP1, KANR, or NATR, and will lack the essential component (Ade, Ura, Trp) or include a drug (G418, NAT). Markers that can detect when a protein is no longer present (for example when the protein is degraded by an external composition) can be referred to as counter-selection markers, such as the URA3 gene, and can be poor or leaky (easily masked by the selection of mutants that escape the selection). This leakiness of the selection marker can lead to a high false positive rate.
Methods and systems of the disclosure can combine a strong negative selection marker with the intracellular stabilization of the production of short peptides or macrocycles to screen for mediators of bridging interactions between a target protein and an E3 ubiquitin ligase. An inducible one-hybrid approach can be employed, which can drive the expression of any one or combination of several cytotoxic reporters (death agents) as well as positive selection markers. A method of the disclosure involving induced expression of a combination of cytotoxic reporters in a one-hybrid system can allow for a multiplicative effect in lowering the false-positive rate of the one-hybrid assay, as all of the cytotoxic reporters must simultaneously be “leaky” to allow for an induced cell to survive.
Disclosed herein, in certain embodiments, is a method for identifying a molecule that can selectively bridge an interaction between a first test protein and an E3 ubiquitin ligase to mediate functional degradation of the test protein in a host cell. A second test protein may be used as a positive control, such as, while the molecule mediates degradation of the first test protein, it may not affect expression of the second test protein. The method may comprise expressing in the host cell a first fusion protein comprising the first test protein and a DNA-binding moiety and a gene activating moiety; an E3 ubiquitin ligase or a fragment thereof or in some cases, the E3 ubiquitin ligase and its associated machinery; and delivering a molecule from a library to the host cell. The host cell may comprise a promoter sequence for controlling expression of a death agent. The promoter may be specific to the DNA-binding moiety in the first fusion protein such that in the absence of the molecule, expression of the death agent is activated. When the molecule is present, the first test protein may be degraded by the E3 ubiquitin ligase.
In some embodiments, a screen to identify a peptide or small molecule that can mediate the degradation of a target protein may involve testing the peptide or small molecule against a population of host cells in which different cells in the population express different E3 ligases. The host cells can then be transformed with or otherwise subjected to a candidate peptide/small molecule from a library. In such cases, each of the host cells may comprise the same target protein and/or death agent. Surviving cells may be sequenced to identify the E3 ligase that successfully interacts with the peptide/small molecule. In another example, each well of an assay may comprise a plurality of different host cells in which different host cell express different E3 ligases. A peptide/small molecule from a library may then be transformed or otherwise introduced into each well for the identification of a peptide/small molecule that successfully interacts with the target protein and leads to cell survival.
Examples of targets for degradation are oncogenic proteins such as K-Ras oncogenic alleles, Cyclin D family, Cyclin E family, c-MYC, EGFR, HER2, PDGFR, VEGF and beta-catenin, or oncogenic variants such as IDH1(R132H, R132S, R132C, R132G, and R132L) or IDH2(R140Q, R172K).
Examples of E3 ubiquitin ligases that can be used on the system can be chosen from a list including, but not limited to multisubunit E3 ligases of the Culin families (CRL1, CRL2, CRL3, CRL4, CRL5, and CRL7) and single subunit E3 ligases of the RING, RING-Between-RING (RBR), and HECT families consisting of, but not limited to Cereblon, Skp2, MDM2, FBXW7, DCAF1, DCAF15, VHL, AFF4, AMFR, ANAPC11, ANKIB1, AREL1, ARIH1, ARIH2, BARD1, BFAR, BIRC2, BIRC3, BIRC7, BIRC8, BMI1, BRAP, BRCA1, CBL, CBLB, CBLC, CBLL1, CCDC36, CCNB1IP1, CGRRF1, CHFR, CNOT4, CUL9, CYHR1, DCST1, DTX1, DTX2, DTX3, DTX3L, DTX4, DZIP3, E4F1, FANCL, G2E3, HACE1, HECTD1, HECTD2, HECTD3, HECTD4, HECW1, HECW2, HERC1, HERC2, HERC3, HERC4, HERC5, HERC6, HLTF, HUWE1, IRF2BP1, IRF2BP2, IRF2BPL, Itch, KCMF1, KMT2C, KMT2D, LNX1, LNX2, LONRF1, LONRF2, LONRF3, LRSAM1, LTN1, MAEA, MAP3K1, MARCH1, MARCH10, MARCH11, MARCH2, MARCH3, MARCH4, MARCH5, MARCH6, MARCH7, MARCH8, MARCH9, Mdm2, MDM4, MECOM, MEX3A, MEX3B, MEX3C, MEX3D, MGRN1, MIB1, MIB2, MID1, MID2, MKRN1, MKRN2, MKRN3, MKRN4P, MNAT1, MSL2, MUL1, MYCBP2, MYLIP, NEDD4, NEDD4L, NEURL1, NEURL1B, NEURL3, NFX1, NFXL1, NHLRC1, NOSIP, NSMCE1, PARK2, PCGF1, PCGF2, PCGF3, PCGF5, PCGF6, PDZRN3, PDZRN4, PELI1, PELI2, PELI3, PEX10, PEX12, PEX2, PHF7, PHRF1, PJA1, PJA2, PLAG1, PLAGL1, PML, PPIL2, PRPF19, RAD18, RAG1, RAPSN, RBBP6, RBCK1, RBX1, RC3H1, RC3H2, RCHY1, RFFL, RFPL1, RFPL2, RFPL3, RFPL4A, RFPL4AL1, RFPL4B, RFWD2, RFWD3, RING1, RLF, RLIM, RMND5A, RMND5B, RNF10, RNF103, RNF11, RNF111, RNF112, RNF113A, RNF113B, RNF114, RNF115, RNF121, RNF122, RNF123, RNF125, RNF126, RNF128, RNF13, RNF130, RNF133, RNF135, RNF138, RNF139, RNF14, RNF141, RNF144A, RNF144B, RNF145, RNF146, RNF148, RNF149, RNF150, RNF151, RNF152, RNF157, RNF165, RNF166, RNF167, RNF168, RNF169, RNF17, RNF170, RNF175, RNF180, RNF181, RNF182, RNF183, RNF185, RNF186, RNF187, RNF19A, RNF19B, RNF2, RNF20, RNF207, RNF208, RNF212, RNF212B, RNF213, RNF214, RNF215, RNF216, RNF217, RNF219, RNF220, RNF222, RNF223, RNF224, RNF225, RNF24, RNF25, RNF26, RNF31, RNF32, RNF34, RNF38, RNF39, RNF4, RNF40, RNF41, RNF43, RNF44, RNF5, RNF6, RNF7, RNF8, RNFT1, RNFT2, RSPRY1, SCAF11, SH3RF1, SH3RF2, SH3RF3, SHPRH, SIAH1, SIAH2, SIAH3, SMURF1, SMURF2, STUB1, SYVN1, TMEM129, Topors, TRAF2, TRAF3, TRAF4, TRAF5, TRAF6, TRAF7, TRAIP, TRIM10, TRIM11, TRIM13, TRIM15, TRIM17, TRIM2, TRIM21, TRIM22, TRIM23, TRIM24, TRIM25, TRIM26, TRIM27, TRIM28, TRIM3, TRIM31, TRIM32, TRIM33, TRIM34, TRIM35, TRIM36, TRIM37, TRIM38, TRIM39, TRIM4, TRIM40, TRIM41, TRIM42, TRIM43, TRIM43B, TRIM45, TRIM46, TRIM47, TRIM48, TRIM49, TRIM49B, TRIM49C, TRIM49D1, TRIM5, TRIM50, TRIM51, TRIM52, TRIM54, TRIM55, TRIM56, TRIM58, TRIM59, TRIM6, TRIM60, TRIM61, TRIM62, TRIM63, TRIM64, TRIM64B, TRIM64C, TRIM65, TRIM67, TRIM68, TRIM69, TRIM7, TRIM71, TRIM72, TRIM73, TRIM74, TRIM75P, TRIM77, TRIM8, TRIM9, TRIML1, TRIML2, TRIP12, TTC3, UBE3A, UBE3B, UBE3C, UBE3D, UBE4A, UBE4B, UBOX5, UBR1, UBR2, UBR3, UBR4, UBR5, UBR7, UHRF1, UHRF2, UNK, UNKL, VPS11, VPS18, VPS41, VPS8, WDR59, WDSUB1, WWP1, WWP2, XIAP, ZBTB12, ZFP91, ZFPL1, ZNF280A, ZNF341, ZNF511, ZNF521, ZNF598, ZNF645, ZNRF1, ZNRF2, ZNRF3, ZNRF4, Zswim2, and ZXDC.
Expression of Proteins in the Host Cells
One or more plasmid constructs may be used to express different proteins in the host cell. The number of plasmids used may depend on the host cell, presence of integrated constructs in the host cell amongst other conditions.
In some cases, a method of identifying a molecule that elicits degradation of a first test protein may use proteins such as: an E3 ubiquitin ligase, a molecule from a library of molecules and a first fusion protein comprising a first test protein, a first DNA-binding moiety and a gene-activating domain. The method may also use a promoter driving the expression of a death agent, such as the promoter sequence is specific for the first DNA-binding moiety. In addition to this scheme, in some cases, the method may also utilize a second fusion protein comprising a second DNA-binding domain and a gene-activating moiety along with a promoter driving the expression of a positive or negative marker such as the promoter sequence is specific for the second DNA-binding moiety.
The proteins and nucleic acid sequences mentioned above may be provided to the host cell in the form of plasmids. In some cases, the nucleic acid sequences of the proteins and nucleic acids comprising the promoter and death agents/positive and negative markers may be integrated into the host cell. In some cases, the molecule from a library of molecules is a small molecule/compound and does not need to be encoded on a plasmid.
For instance, in one example, the first fusion protein may be provided in a plasmid (Plasmid 1), the E3 ubiquitin ligase may be provided in a separate plasmid (Plasmid 2) and the DNA encoded molecule from a library may be provided in a separate plasmid (Plasmid 3). All three plasmids may be transfected into a plurality of host cells. In cases where a second fusion protein is also being used, the second fusion protein may be provided in plasmid 1 or in a separate plasmid (Plasmid 4). The expression constructs of the plasmids may also be combined in one or two plasmids to reduce the number of plasmids to be transfected. Additionally, the constructs comprising the promoters driving the death agent or the positive/negative selection markers may also be provided in the plasmids or otherwise, they may be integrated into the host cell.
In another instance, the first fusion protein may be genetically integrated into the host cell whereas Plasmids 2 and 3 comprising the E3 ubiquitin ligase and the molecule from the library of molecules are transfected into the host cell. In this example, the second fusion protein may also be integrated into the host cell or in some cases, be provided as a plasmid.
In yet another instance, the first fusion protein and the E3 ubiquitin ligase are both integrated into the host cell and the molecule from the library of molecules is transfected in the form of a plasmid into the host cell. The second fusion protein, as mentioned above, may be integrated into the host cell or it may be provided in a plasmid form. The constructs comprising the promoters driving the death agent or the positive/negative selection markers may also be provided in the plasmids or otherwise, they may be integrated into the host cell.
In another instance, the first fusion protein may be transfected in a plasmid for/integrated into the host cell but an endogenous E3 ubiquitin ligase is used in which case, the integration or transfection of a plasmid containing the E3 ligase may not be needed.
In some cases, the nucleic acid sequences for the fusion protein/proteins, the E3 ubiquitin ligase, the promoter driving the death agent (and promoter driving the positive/negative selection marker, if it is being used) may all be integrated into the host cell. In this case, just a single plasmid comprising the molecule from a library of molecules may be transfected into the host cell.
In some embodiments, the host cell or cells disclosed herein comprises a plasmid vector. The plasmid can contain, for example, two restriction sites that enable the integration of two proteins that constitute the bait and E3 ligase of interest. The bait protein of interest can involve an oncogene (such as Cyclin E family, Cyclin D family, c-MYC, EGFR, HER2, K-Ras, PDGFR, Raf kinase, and VEGF). The bait protein of interest can involve an effector of an inflammatory response (such as IL-17RA, IL-17RB, IL-17RC, IL17-RD, IL17-RE, Act1 (CIKS), and IL-23R).
A plasmid can be configured to express two proteins that constitute the bait and E3 ligase of interest and an additional factor, for example, a variant of one of the bait protein. The variants for targeting can be KRAS (G12D, G12V, G12C, G12S, G13D, Q61K, or Q61L, etc.) and the control variant is WT KRAS. The additional factor can also be another protein bound to the bait protein, or another target of the E3 ligase.
In some embodiments, the host cell disclosed herein comprise a plasmid wherein a DNA sequence encoding a first polypeptide is inserted in frame with Gal4-DBD and in frame with VP64-AD, and a DNA sequence encoding for a second polypeptide comprising of an E3 ubiquitin ligase.
In some embodiments, the first test protein is a variant of KRAS, the E3 ubiquitin ligase is VHL.
A plasmid can encode for the fusion of an activation domain or another gene activating moiety and a DBD to each protein driven by either a strong promoter and terminator (such as ADH1), or by an inducible promoter (such as GAO. Other exemplary activation domains include those of VP16 and B42AD. In some embodiments, the DNA binding moiety is derived from LexA, TetR, Lad, Gli-1, YY1, glucocorticoid receptor, or Ume6 domain and the gene activating moiety is derived from Gal4, B42, or VP64, Gal4, NF-κB AD, Dof1, BP64, B42, or p65. Each protein fusion can be tagged for subsequent biochemical experiments with, for example, a FLAG, HA, MYC, or His tag. The plasmid can also include bacterial selection and propagation markers (i.e. ori and AmpR), and yeast replication and selection markers (i.e. TRP1 and CEN or 2 um). The plasmid may contain multiple bait proteins fused to different DBDs and ADs. The plasmid can also be integrated into the genome at a specified locus.
Disclosed herein, in certain embodiments, is a library of plasmid vectors, each plasmid vector comprising: a DNA sequence encoding a different peptide sequence operably linked to a first switchable promoter; a DNA sequence encoding a death agent under control of a second switchable promoter; and a DNA sequence encoding a positive selection reporter under control of a third switchable promoter.
Expression of Selection Markers
Positive Selection Markers
An efficient expression of a test protein can direct a RNA polymerase to a specific genomic site, and allow expression of a protein that enables an organism to grow on selection media. The selection media can be specific to, for example, ADE2, URA3, TRP1, KANR, or NATR, and can lack the essential component (Ade, Ura, Trp) or can include a drug (G418, NAT). A plasmid can encode for one or more positive selection markers that enable an organism to grow on selection media.
Negative Selection Markers
An inducible one-hybrid approach can be employed, which can drive the expression of any one or combination of several cytotoxic reporters (death agents) as well as positive selection markers. A method of the disclosure involving induced expression of a combination of cytotoxic reporters in a one-hybrid system can allow for a multiplicative effect in lowering the false-positive rate of the one-hybrid assay, as all of the cytotoxic reporters must simultaneously be “leaky” to allow for an induced cell to survive. The cytotoxic reporters can be comprised or contain domains of various polypeptides, for example as shown in Table 1.
enterica)
pneumoniae)
pyogenes)
syringae)
In some embodiments, the death agent is an overexpressed product of genetic element selected from DNA or RNA. In some embodiments, the genetic element is a Growth Inhibitory (GIN) sequence such as GIN11.
In some embodiments, the death agent is a ribosomally encoded xenobiotic agent, a ribosomally encoded poison, a ribosomally encoded endogenous or exogenous gene that results in severe growth defects upon mild overexpression, a ribosomally encoded recombinase that excises an essential gene for viability, a limiting factor involved in the synthesis of a toxic secondary metabolite, or any combination thereof. In some embodiments, the ribosomally encoded death agent is Cholera toxin, SpvB toxin, CARDS toxin, SpyA Toxin, HopUl, Chelt toxin, Certhrax toxin, EFV toxin, ExoT, CdtB, Diphtheria toxin, ExoU/VipB, HopPtoE, HopPtoF, HopPtoG, VopF, YopJ, AvrPtoB, SdbA, SidG, VpdA, Lpg0969, Lpg1978, YopE, SptP, SopE2, SopB/SigD, SipA, YpkA, YopM, Amatoxin, Phallacidin, Killer toxin KP1, Killer toxin KP6, Killer Toxin K1, Killer Toxin K28 (KHR), Killer Toxin K28 (KHS), Anthrax lethal factor endopeptidase, Shiga Toxin, Saporin Toxin, Ricin Toxin, or any combination thereof. The cytotoxic reporter or death agent may be a protein with a sequence selected from SEQ ID Nos: 1-41. The cytotoxic reporter may be a variant of a naturally found cytotoxic reporters. Such a variant can have at least 70%, 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, or 99% sequence identity to SEQ ID NOs: 1-41.
Along with one or more positive selection markers, a plasmid can also include one or more negative selection markers under control of a different DNA binding sequence to enable binary selection. The plasmid can encode for one or more of negative selection markers in Table 1 driven by a promoter which depends on the DBD present in the bait protein integration plasmid—DNA Binding Sequence (DBS), for example, the LexAop sequence (DBS) which can become bound by LexA (DBD). In some embodiments, to ensure repression of the ‘death agents,’ the plasmid can include a silencing construct such as a TetR′-Tup11 fusion driven by a strong promoter (such as ADH1) to bind the DBD and silence transcription in the presence of doxycycline. The plasmid can comprise bacterial selection and propagation markers (i.e. ori and AmpR), and yeast replication and selection markers (i.e. LEU2 and CEN or 2-micron) as well.
Disclosed herein, in certain embodiments, is a library of plasmid vectors, each plasmid vector comprising a DNA sequence encoding a different peptide sequence operably linked to a first switchable promoter; a DNA sequence encoding a death agent under control of a second switchable promoter; and a DNA sequence encoding a positive selection reporter under control of a third switchable promoter. Plasmids comprising a promoter driving different E3 ubiquitin ligases may also be included in the library of vectors.
Addition or Expression of Modulators
A molecule from a library that can selectively bridge a bait protein of interest and a specific E3 ubiquitin ligase leading to the bait protein degradation can be screened by use of positive and/or negative selection markers in a host cell.
In some embodiments, the molecule is small molecule. In some embodiments, the small molecule is peptidomimetic. The host cell can be made to become permeabilized to small molecules, for example by deletion of drug efflux pump encoding genes such as PDR5. Genes encoding for transcription factors such as PDR1 and PDR3 that induce expression of efflux pumps including but not restricted to the 12 genes described by 12geneΔ0HSR (Chinen, 2011). The host cell could be further permeabilized to small molecules by interference with the synthesis and deposition of ergosterol in the plasma membrane such as by the deletion of ERG2, ERGS, and/or ERG6 or driving their expression under a regulatable promoter.
In other embodiments, the molecule is a peptide, macrocycle or protein. In some embodiments, the peptide or protein is derived from naturally occurring protein product. In another embodiment, the peptide or protein is a synthesized protein product. In other embodiments, the peptide or protein is a product of recombinant genes.
In some embodiments, the molecule is introduced to the host cell exogenously. In other embodiments, the molecule is the expression product of test DNA inserted into the host cell, wherein the test DNA comprises of DNA sequences that encodes a polypeptide. DNA encoded libraries can be formed by delivery of a plurality of test DNA molecules into host cells. In some embodiments, the peptide sequences of the polypeptides in the library are random. In some embodiments, the different peptide sequences are pre-enriched for binding to a target.
To screen for peptides that selectively facilitate the degradation of a protein of interest, peptides from a randomized peptide library can be applied to or expressed internally from the host cell. A plasmid can be further used to express a randomized peptide library (such as a randomized NNK 60-mer sequences). The plasmid can include a restriction site for integration of a randomized peptide library driven by a strong promoter (such as the ADH1 promoter) or an inducible promoter (such as the GAL1 promoter).
In some embodiments, the randomized peptide library is about 60-mer. In some embodiments, the randomized peptide library is from about 5-mer to 20-mer. In some embodiments, the randomized peptide library is less than 15-mer.
The library can also initiate with a fixed sequence of, for example, Methionine-Valine-Asparagine (MVN) for N-terminal stabilization and/or another combination of high-half-life N-end residues (see, for e.g., Varshaysky. Proc. Natl. Acad. Sci. USA. 93:12142-12149 (1996)) to maximize the half-life of the peptide, and terminate with the 3′UTR of a short protein (such as sORF1). The peptide can also be tagged with a protein tag such as Myc. In some embodiments, N-terminal residues of the peptide comprise Met, Gly, Ala, Ser, Thr, Val, or Pro or any combination thereof to minimize proteolysis.
The plurality of different short peptide sequences can be randomly generated by any method (e.g. NNK or NNN nucleotide randomization). The plurality of different short peptide sequences can also be preselected, either by previous experiments selecting for binding to a target, or from existing data sets in the scientific literature that have reported rationally-designed peptide libraries.
In some embodiments, the library comprises polypeptides about 60 amino acids or fewer in length. In another embodiment, the library comprises polypeptides about 30 or fewer amino acids in length. In another embodiment, the library comprises polypeptides about 20 or fewer amino acids in length.
Modification of Facilitating Peptides
The peptide that leads to the selective degradation of the target can also be a product of post-translational modifications. The post-translational modification can include any one or combination of cleavage, cyclization, bi-cyclization, methylation, halogenation, glycosylation, acylation, phosphorylation, and acetylation. In some embodiments, the methylation comprises reacting with an N-methyltransferase. In some embodiments, the post-translational modification is done by naturally occurring enzymes. In some embodiments, the post-translational modification is done by synthetic enzymes. In some embodiments, the synthetic enzymes are chimeric.
The peptide can be ribosomally synthesized and post-translationally modified peptide (RiPP) whereby the core peptide is flanked by prepropeptide sequence comprising a leader peptide and recognition sequences which signal for the recruitment of maturation, cleavage, and/or modifying enzymes such as excision or cyclization enzymes including, for example, lanthipeptides maturation enzymes from Lactococcus lactis (LanB, LanC, LanM, LanP) patellamide biosynthesis factors from cyanobacteria (PatD, PatG), butelase 1 from Clitoria ternatea, and POPB from Galerina marginata, Lentinula edodes, Omphalotacae olearis, Dendrothele bispora, or Amanita bisporigera, or other species. In some embodiments, the cyclization or bicyclization enzymes are synthetic chimeras.
In one example, the variable peptide library region is embedded within the primary sequence of a modifying enzyme (e.g., the homolog of the omphalotin N-methyltransferase enzyme from Dendrothele bispora, Marasmius fiardii, Lentinula edodes, Fomitiporia mediterranea, Omphalotus olearius or other) and contains random residues, some of which may be post-translationally decorated by additional modifications like hydroxylation, halogenation, glycosylation, acylation, phosphorylation, methylation, acetylation. This diversified variable region is excised and modified to form N-to-C cyclized, optionally backbone N-methylated macrocycles by the action of a prolyl endopeptidase belonging to the PopB family and N-methyltransferases belonging to the omphalotin methyltransferase family. An exemplary list of prolyl endopeptidases is shown in Table 2. The prolyl endopeptidases may be a protein with a sequence selected from SEQ ID NOs: 42-58. The prolyl endopeptidases may be encoded by a nucleotide sequence selected from SEQ ID NOs: 59 or 60. The prolyl endopeptidase may be a variant of a naturally found prolyl endopeptidases. Such a variant can have at least 70%, 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, or 99% sequence identity to SEQ ID NOs: 42-58. An exemplary list of N-methyltransferases is shown in Table 3. The methyltransferase may be a protein with a sequence selected from SEQ ID Nos: 61-116. The methyltransferases may be encoded by a nucleotide sequence selected from SEQ ID Nos: 117 or 118. The prolyl endopeptidase may be a variant of a naturally found methyltransferases. Such a variant can have at least 70%, 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, or 99% sequence identity to SEQ ID NOs: 61-116.
Galerina
marginata
Amanita
bisporigera
Hypsizygus
marmoreus]
Conocybe
apala
Amanita
bisporigera
Lentinula
edodes
Omphalotacae
olearis
Gymnopus
fusipes
Lentinula
novae-
zelandiae
Lentinula
raphanica
Lentinula
lateritia
Dendrothele
bispora
Dendrothele
bispora
Gypsophila
vaccaria
Gymnopus
fusipes
Lentinula
edodes
Omphalotus
olearis
Gymnopus
fusipes
Gymnopus
fusipes
Anomoporia
bombycina
Armillaria
gallica
Armillaria
gallica
Arthrobotrys
oligospora
Armillaria
ostoyae
Apodospora
peruviana
Bjerkandera
adusta
Cercospora
beticola
Ceratobasidium
Ceratobasidium
Cerrena
unicolor
Cerrena
unicolor
Cladosporium
fulvum
Chalara
longipes
Coprinopsis
marcescibilis
Coprinellus
micaceus
Cystostereum
murrayi
Coprinellus
pellucidus
Dendrothele
bispora
Dendrothele
bispora
Fomitiporia
mediterranea
Fomitiporia
mediterranea
Fomitiporia
mediterranea
Fomitiporia
mediterranea
Gyromitra
esculenta
Gymnopilus
junonius
Gymnopus
fusipes
Hydnomerulius
pinastri
Lentinula
edodes
Lentinula
lateritia
raphanica
Mycosphaerella
eumusae
Marasmius
fiardii
Mycena
rosella
Mycena
rosella
Omphalotus
olearius
Phlebiopsis
gigantea
Phlebiopsis
gigantea
Pseudocercos
pora musae
Porodaedalea
chrysoloma
Rhizopogon
vinicolor
Rhizopogon
vinicolor
Rhizopogon
vinicolor
Rhizopogon
vinicolor
Rhizopogon
vinicolor
vinicolor
Rhizopogon
vinicolor
Rhizopogon
vinicolor
Sanghuangporus
baumii
Serendipita
vermifera ssp.
bescii
Thanatephorus
cucumeris
Trypethelium
eluteriae
Trichophaea
hybrida
Talaromyces
islandicus
Wilcoxina
mikolae
Lentinula
novae-
zelandiae
Gymnopus
fusipes
Gymnopus
fusipes
Gymnopeptide A (GymA) and Gymnopeptide B (GymB) are two related multiply N-methylated cyclic octadecapeptides that were isolated from the spindleshank mushroom Gymnopus fusipes (G. fusipes) (also known as Collybia fusipes). GymA and GymB differ at one position (serine for GymA vs. threonine for GymB). Several aggressive adherent cancer cell lines (e.g. HeLa, A431, T47D, MCF7, MDA-MB-231) exhibit hypersensitivity to both GymA and GymB, with IC50 values in the low nanomolar range.
It was surprising to discover that rather than utilizing an NRPS to synthesize these peptide macrocycles, the genome of G. fusipes encodes for one gene containing a nucleic acid sequence that encodes the 18 amino acids of GymB. The 18-amino acids sequence lies at the C-terminus of an open reading frame that encodes for a putative S-Adenosylmethionine (SAM) dependent methyltransferase. Hereinafter, the gene encoding for the methyltransferase followed by the GymB peptide sequence cassette is referred to as the gymnopeptide precursor gene, GymMAB.
The GymMAB gene is present in a cluster that also includes another open reading frame encoding a prolyl-oligopeptidase (GymP), which cleaves and cyclizes the methylated gymnopeptide cassettes. These enzymes bear weak resemblance to the G. marginata and Amanita species prolyl-oligopeptidase PopB proteins and the O. olearis omphalotin-producing enzymes, and form a distinct family of RiPPs/RiPP-processing-enzymes with unique structural and functional features that allow them to accommodate the relatively large-sized 18-mer macrocycle.
Furthermore, careful examination of several Gymnopus species that are closely related to G. fusipes, such Gymnopus earle, Gymnopus dryophilus, Gymnopus ocior, Gymnopus acervatus, Gymnopus luxurians, Gymnopus androsaceus (also known as Marasmius androsaceus or Setulipes androsaceus) Micromphale foetidum, Micromphale perforans, Marasmius fiardii. Rhodocollybia maculata, and Rhodocollybia butyracea failed to detect any genes that encode for orthologs or other related genes to the aforementioned enzymes identified in G. fusipes. On the other hand, the biosynthetic gene cluster of enzymes involved in the production of the omphalotins are present in a wide group of closely related species such as Omphalotous olivascens as well as Lentinula species, including Lentinula edodes, Lentinula aciculospora, Lentinula raphanica, Lentinula novae-zelandiae, Lentinula boryana, and Lentinula lateritia. Thus, the identified genetic cluster appears to be horizontally transferred.
Enzymes such as the methyltransferase and prolyloligopeptidase isolated from species such as G. fusipes can be used to generate methylated macrocycles. The methylated macrocycles may be screened using the methods described herein. The enzymes can be integrated into host cells and used to generate DNA-encoded libraries of RiPPs. The enzymes can also be used to manufacture specific macrocycles of interest at scale in heterologous prokaryotic or eukaryotic expression systems. Uses of the enzymes in heterologous expression systems may include, but are not limited to, reverse Y2H systems as described in PCT/US2018/061292 (published as WO 2019/099678) and U.S. application Ser. No. 15/683,586 (published as US20170368132A1), which are hereby incorporated by reference in their entireties (and in particular with respect to the reverse hybrid and related yeast systems disclosed therein).
The macrocycles generated using the methods described herein may be used as drugs. Such drugs may be used for the treatment of various diseases or conditions. The macrocycles generated using the methods described herein may be used to modulate protein-protein interaction between a first and second protein. The macrocycles generated using the methods described herein may be used to disrupt protein-protein interaction between a first and second protein.
Disclosed herein, in certain embodiments, is a method of detection or degradation of a target protein that is mediated by a molecule that links a first target or test protein to a second target protein in a host cell, comprising: expressing in the host cell a first fusion protein comprising the first test protein, a second protein; delivering a first molecule to the host cell; modifying the first molecule while in the host cell via a modifying enzyme, such as a prolyloligopeptidase and/or a methyltransferase; and allowing the first molecule to bridge the interaction between the first test protein and the second protein, wherein the first molecule is a product of an encoded DNA sequence, wherein the first molecule comprises a randomized polypeptide library and one or more modifying enzymes, wherein the one or more modifying enzymes modify the randomized polypeptide library.
The prolyloligopeptidases described herein may be ones that are able to macrocyclize relatively large peptides. The prolyloligopeptidases described herein may be ones that are able to macrocyclize peptides comprising at least 5 amino acids, at least 7 amino acids, at least 10 amino acids, at least 15 amino acids, at least 18 amino acids, at least 20 amino acids or at least 25 amino acids. The prolyloligopeptidases described herein may be ones that are able to macrocyclize peptides comprising at most 7 amino acids, at most 10 amino acids, at most 15 amino acids, at most 18 amino acids, at most 20 amino acids or at most 25 amino acids.
The tryptophan at position 603 appears to be highly conserved in relative prolyloligopeptidases that are not capable of relatively large macrocyclizing peptides. Similarly, the asparagine at position 563, adjacent to the active site serine at position 562, is also conserved in these same prolyloligopeptidases. “Position 603” and “Position 563”, as used herein, refer to the position of the active-site tryptophan and the position of the asparagine adjacent to the active-site serine in the prolyloligopeptidase of SEQ ID NO: 55, respectively, along with corresponding amino acid in other prolyloligopeptidases. In other words, position 603 or position 563 of a prolyloligopeptidase that differs from SEQ ID NO: 55 may not necessarily be the 603rd or 563rd amino acid in that protein, but rather is the position that aligns with position 603 or 563 of SEQ ID NO: 55 when the prolyloligopeptidase is aligned with it, regardless of the distance of that amino acid from the N-terminus of the protein. Without being bound by theory, the mutation of these highly conserved tryptophan and asparagine residues to other amino acids, such as leucine and serine, respectively, may be key to enable its structural flexibility to accommodate peptides such as the larger 18-mer gymnopeptides. Additionally, the substitution of tryptophan at position 603 with another residue such as leucine may play an important role in expanding the cleavage site recognition specificity of the oligopeptidase from being directed towards small secondary amine residues such as proline or sarcosine (N-methyl-glycine) to enable cleavage at secondary amine sites with bulkier side chains such as N-methyl-valine, N-methyl-isoleucine, or N-methyl-leucine. Consistent with this premise, while the N-terminal cut site of the Gymnopeptides AB precursor protein is at a proline residue, the C-terminal cut site is at a methyl-valine residue. Prolyloligopeptidases belong to the family of serine proteases. The mechanism of action of serine peptidases involves an acyl enzyme intermediate. Both the formation and the decomposition of the acyl enzyme proceed through the formation of a negatively charged tetrahedral intermediate that is stabilized by the oxyanion binding site providing two hydrogen bonds to the oxyanion. In prolyloligopeptidases one of the hydrogen bonds is formed between the oxyanion and the main chain amide group of asparagine 563, which is directly adjacent to the catalytic serine, serine 562. The second hydrogen bond is among this type of serine peptidases and is provided by the hydroxyl group of tyrosine 481 (position 481 of SEQ ID NO:55). In the chymotrypsin-type members of the serine protease family of enzymes the hydrogen bonds are contributed by the main chain amide groups of the catalytic serine residue and that of a glycine residue that is at a −2 position from the catalytic serine. The substitution of the highly conserved asparagine at position 563 with serine renders the serine 563 residue and the glycine 561 residue (position 561 of SEQ ID NO:55) positioned identically to the active site serine and glycine hydrogen bond donors of chymotrypsin-type proteases. This substitution may play an important role to enable the enzyme to toggle between using two different active-site serines for each of the two cleavage events, for example serine 562 could be the active site residue involved in the N-terminal proline-directed cut with the two hydrogen bonds to the oxyanion contributed by the main chain amide of the serine residue at position 563 and the hydroxyl group of the tyrosine at position 481, while serine 563 is the active site residue involved in the second N-methyl-valine directed cut with the two hydrogen bonds to the oxyanion contributed by the main chain amides of serine at position 563 and glycine at position 561, or vice versa. The combination of this novel wider catalytic pocket due the substitution of tryptophan 603 with leucine and a toggle-switchable active site serine due to the substitution of asparagine 563 with serine render this new oligopeptidase particularly suited at recognizing a wide variety of secondary amine residues with bulky side chains at the cleavage site and incorporate larger sizes of macrocycles than any of the previously characterized members of the family. Shown in
In some cases, the tryptophan residue in the active site of a prolyloligopeptidase, which corresponds to the conserved tryptophan at position 603 of SEQ ID NO: 55, may be replaced with a different amino acid residue. For instance, in some cases the tryptophan residue in the active site of a prolyloligopeptidase may be replaced with a leucine residue. In some cases, the prolyloligopeptidases used herein do not comprise a tryptophan residue at the 603 position in the active site of the enzyme, wherein the position 603 corresponds to the active site of SEQ ID NO: 55.
In some cases, the asparagine residue in the active site of a prolyloligopeptidase, which corresponds to the conserved asparagine at position 563 of SEQ ID NO: 55, may be replaced with a different amino acid residue. For instance, in some cases the asparagine residue in the active site of a prolyloligopeptidase may be replaced with a serine residue. In some cases, the prolyloligopeptidases used herein do not comprise a asparagine residue at the 563 position in the active site of the enzyme, wherein the position 563 corresponds to the active site of SEQ ID NO: 55.
In other embodiments, the cyclization comprises reacting with beta-lactamase. A variable region is excised and end-to-end cyclized by the actions of an N-methyltransferase and a beta-lactamase family member. Table 4 shows an exemplary list of lactamase and amino acid sequences of the processed cyclic peptides. The lactamase may be a protein with a sequence selected from SEQ ID NOs: 119-120. The lactamase may be a variant (e.g., a non-natural variant) of a naturally occurring lactamase. Such a variant can have at least 70%, 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, or 99% sequence identity to SEQ ID NOs: 119-120. In some embodiments, some of the sidechains of the randomized residues are subsequently isomerized from the L- to D-configuration or decorated with additional modifications like hydroxylation, halogenation, glycosylation, acylation, phosphorylation, methylation, and acetylation.
Rhizophogun
vinicolor
Rhizophogun
vinicolor
Rhizophogun
vinicolor
Rhizophogun
vinicolor
In some embodiments, the cyclization comprises reacting with a prolyl endopeptidase, an N-methyltransferase, and a hydroxylase. In some embodiments, the bicyclization comprises further modification of the indicated anchored residues on the cyclized peptide, forming an internal tryptathionine bridge. The first step may involve hydroxylation of the 2-position of the indole ring of the tryptophan residue by a hydroxylase belonging to the cytochrome P450 family of oxygenases. An example of such hydroxylase is shown in TABLE 5. The hydroxylase may be a protein with a sequence selected from SEQ ID NO: 123. The hydroxylase may be a variant (e.g., a non-natural variant) of a naturally found hydroxylase. Such a variant can have at least 70%, 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, or 99% sequence identity to SEQ ID NO: 123.
Galerina
marginata
Step 2 may involve the formation of a tryptathionine bridge between the 2′-hydroxyl position on tryptophan and the thiol group from the cysteine residue. This condensation reaction is catalyzed by a novel family of dehydratases. Examples of the dehydratases are shown in TABLE 6. The dehydratases may be a protein with a sequence selected from SEQ ID NOs: 124-127. The dehydratases may be a variant (e.g., a non-natural variant) of a naturally found dehydratases. Such a variant can have at least 70%, 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, or 99% sequence identity to SEQ ID NOs: 124-127.
Galerina
marginata
Galerina
marginata
Hypsizygus
marmoreus
Galerina
marginata
Step 3 describes S-oxygenation of the tryptathionine thiol by a flavin-monoxygenase enzyme that converts it to a sulfinyl form. Examples of such monoxygenase are shown in TABLE 7. Step 4 describes potential future modification steps such as hydroxylation of side chains on the peptide such as the hydroxylation of position 6 on the indole ring of the tryptathionine-forming tryptophan residue by a P450 family monoxygenase. The monoxygenase may be a protein with a sequence selected from SEQ ID NO: 128. The monoxygenase may be a variant (e.g., a non-natural variant) of a naturally found monoxygenase. Such a variant can have at least 70%, 75%, 80%, 85%, 90%, 95%, 96%, 97%, 98%, or 99% sequence identity to SEQ ID NO: 128.
Galerina
marginata
The sequence which flanks the encoded random peptide library can be modified by using N-term and C-term flanks from the MSDIN family genes (toxin preproprotein sequences) identified in the genomes of Amanita bisporigera and Amanita phalloides.
The enzymes can additionally be targeted to a specific cellular compartment to increase peptide synthesis efficiency and increase yield for peptide production purposes.
Disclosed herein, in certain embodiments, is a method of detecting degradation of a target protein that is mediated by a molecule that links a target or test protein to an E3 ubiquitin ligase in a host cell, comprising: expressing in the host cell a first fusion protein comprising the first test protein, an E3 ubiquitin ligase; delivering a first molecule to the host cell; modifying the first molecule while in the host cell via a modifying enzyme; and allowing the first molecule to bridge the interaction between the first test protein and the E3 ubiquitin ligase, wherein the first molecule is a product of an encoded DNA sequence, wherein the first molecule comprises a randomized polypeptide library and one or more modifying enzymes, wherein the one or more modifying enzymes modify the randomized polypeptide library.
Host Cells
In some embodiments, the host cell is a eukaryote or a prokaryote. In some embodiments, the host cell is from animal, plant, a fungus, or bacteria. In some embodiments, the fungus is Aspergillus or Pichia pastoris. In some embodiments, the host cell is a haploid yeast cell. In other embodiments, the host cell is a diploid yeast cell. In some embodiments, the diploid yeast cell is produced by mating a first host cell comprising DNA sequences encoding the first chimeric gene, the second chimeric gene, and the third chimeric gene, to a second host cell comprising DNA sequences encoding the death agent, positive selection reporter, and the mRNA comprising a nucleotide sequence encoding a polypeptide. In some embodiments, the plant is Nicotiana tabacum or Physcomitrella patens. In some embodiments, the host cell is a sf9 (Spodoptera frugiperda) insect cell.
Disclosed herein, in certain embodiments, is a host cell configured to express a first fusion protein comprising a first test protein, a first DNA-binding moiety and a first gene activating moiety; an E3 ubiquitin ligase; a death agent, wherein the expression of the death agent is under control of a promoter DNA sequence specific for the DNA-binding moiety and a polypeptide of 60 or fewer amino acids, wherein the polypeptide modulates an interaction between the first test protein and the E3 ubiquitin ligase to lead to the first test protein's accelerated degradation.
In some embodiments, the host cell may also comprise a second fusion protein, comprising a second DNA-binding moiety, a second test protein, and a second gene-activation moiety; and a positive selection reporter, wherein the expression of the positive reporter is under control of a second promoter DNA sequence specific for the second DNA-binding moiety.
The host cell may have a mutant background enabling uptake of small molecules. In some cases, the host cell has a mutant background enabling increased transformation efficiency.
Disclosed herein, in certain embodiments, is a host cell comprising a plasmid vector wherein a DNA sequence encoding a first polypeptide is inserted in frame with Gal4-DBD and VP64-AD, and a second polypeptide is inserted in frame with LexA-DBD and VP64-AD, and wherein a DNA sequence encodes an E3 ubiquitin ligase.
Disclosed herein, in certain embodiments, is a kit comprising of the described plasmids; and transfectable host cells compatible with the plasmids, or any combination thereof. In some embodiments, the provided host cells are already transfected with components of the plasmids. In some embodiments, the kit includes selectable agents for use with host cells transfected with the plasmids. In some embodiments a library of variants of either plasmid are provided, wherein more than a single pair of bait proteins or E3 ubiquitin ligases are provided. Such a library can be used to, for example, screen for agents with selective protein targeting. In some embodiments a library of variants of the polypeptide plasmid are provided, wherein a plurality of different short test polypeptide sequences for screening are provided. The plurality of different short peptide sequences can be randomly generated by any method (e.g. NNK or NNN nucleotide randomization). The plurality of different short peptide sequences can also be preselected, either by previous experiments selecting for binding to a target, or from existing data sets in the scientific literature that have reported rationally-designed peptide libraries.
The host cell can additionally be made to be permeable to small molecules, for example by deletion of drug efflux pump encoding genes such as PDR5. Genes encoding for transcription factors such as PDR1 and PDR3 that induce expression of efflux pumps including but not restricted to the 12 genes described by 12geneΔ0HSR (Chinen, 2011). The host cell could be further permeabilized to small molecules by interference with the synthesis and deposition of ergosterol in the plasma membrane such as by the deletion of ERG2, ERGS, and/or ERG6 or driving their expression under a regulatable promoter.
The host cell can additionally carry mutations to enable more efficient transformation with vectors and/or more efficient uptake small molecules.
The mentioned plasmids can be used in various permutations. In some embodiments, integration of the plasmids into the genome of the host cell is followed by transformation of a library with randomly encoded peptides using, for example, NNK or NNN codons.
In some embodiments, to perform a screen to identify a peptide that can mediate the degradation of a target protein, the host cell is propagated in selection media to ensure the presence of the required plasmids and expression of a non-target protein (e.g. on media lacking the positive selection marker for yeast, or in media containing antibiotic for human or bacterial cells). This host cell can then be transformed with the peptide library plasmid, and immediately transferred to selection media to ensure all components are present (i.e. on media lacking both plasmid selection markers for yeast, or antibiotics for bacterial or mammalian cells), and are inducing expression of any inducible component such as the target protein which activates expression of the death agent (e.g. with Gal, doxycycline, etc).
In other embodiments, the plasmids are used as a ‘plug and play platform’ utilizing the yeast mating type system, where the one or more (or two or more) plasmids (or the genetic elements therein) are introduced into the same cell by cell fusion or cell fusion followed by meiosis instead of transfection. This cell fusion involves two different yeast host cells bearing different genetic elements. In this embodiment, yeast host cell 1 is one of MATa or MATalpha and includes an integration of the target protein and E3 ubiquitin ligase plasmid. In this embodiment, yeast host cell 1 strain can be propagated on positive selection media to ensure the proteins are present. In this embodiment, the yeast host cell 2 can be the opposite mating type. This strain carries (or has integrated) the randomized peptide library and ‘death agent’ (e.g. cytotoxic reporter) plasmid. Yeast host cell 2 can be generated via large batch high efficiency transformation protocols which ensure a highly diversified library variation within the cell culture. Aliquots of this library batch can then be frozen to maintain consistency. In this embodiment, the strains are mated in batch to result in a diploid strain that carries all the markers, the target protein, E3 ligase, positive selection, ‘death agents’ and peptide. This batch culture then can be propagated on solid medium that enables selection of all the system components (i.e. media lacking both positive selection markers) and inducing expression of any inducible component (i.e. with Gal).
Surviving colonies from limiting dilution experiments performed on host cells bearing both the target protein and E3 ligase and library/cytotoxic constructs (either introduced to the cell by transfection or mating) can constitute colonies with a specific target protein has been degraded by a peptide and no longer triggers the death cascade triggered by the encoded ‘death agents’ (e.g. cytotoxic reporters) while maintaining the expression of a bait variant protein driving a positive selection marker. The peptide sequence can be obtained by DNA sequencing the peptide-encoding region of the plasmid in each surviving colony.
To ensure that survival is due to the degradation of the target rather than stochastic chance or faulty gene expression, an inducible promoter can be used to inactivate the production of either the E3 ligase or the peptide and confirm specificity. In some embodiments, cell survival is observed only on media with galactose wherein all the components are expressed; and no survival is observed on media without galactose when expression of the peptide is lost.
The plasmids can also be isolated and re-transformed into a fresh host cell to confirm specificity. Biochemical fractionation of the viable host cells which contain the target, E3 ligase, peptide, positive selection and ‘death agent’ followed by pull-down experiments can confirm an interaction between the peptide sequence and either target protein or E3 ligase using encoded tags that are part of the fusion constructs (e.g. Myc-tag, HA-tag, His-tag). This is also helpful to perform SAR to determine the binding interface.
The peptides to be used in the screening assay can be derived from a complex library that involves post-translational modifying enzymes. The modified peptides can be analyzed by methods such as mass spectrometry, in addition being sequenced to ID the primary sequence. The peptides can also be tested for inherent membrane permeability by reapplying them onto the host cells exogenously (from a lysate) and observing for reporter inactivation or activation.
Once enough surviving host cell colonies are sequenced, highly conserved sequence patterns can emerge and can be readily identified using a multiple-sequence alignment. Any such pattern can be used to ‘anchor’ residues within the library peptide insert sequence and permute the variable residues to generate diversity and achieve tighter binding. In some embodiments, this can also be done using an algorithm developed for pattern recognition and library design. Upon convergence, the disrupting peptide pattern, as identified through sequencing, can be used to define a peptide disruptor sequence. Convergence is defined by the lack of retrieval of any new sequences in the last iteration relative to the penultimate one.
In some embodiments, a peptide library may be generated and/or used for screening as described herein. The peptides in the generated library may be peptide having drug-like properties. The peptides to be used in the screening assay can be derived from a process that involves enzymes that modify peptides post-translation. For instance, to generate libraries of peptides that have an N-methylated backbone or are macrocyclic in structure, a methyltransferase (such as the ones described in Table 3) may be used to generate the library, along with a prolyloligopeptidase (such as the ones described in Table 2) as shown in
In an alternative approach, to generate libraries of drug-like N-methylated and/or macrocyclic peptides (e.g., for use in a system designed to identify “bridging” peptides or peptides that inhibit a protein-protein interaction), a methyltransferase (such as the ones described in Table 3) may be used, where a protease cleavage site (such as TEV protease) is inserted upstream of the diversified core peptide sequence as shown in
This is an example of a system that uses two variants of one protein, fused to different DBDs to identify facilitator for a specific variant degradation. An integration plasmid is used to integrate into Saccharomyces cerevisiae proteins that constitute the proteins of interest and an E3 ligase. The plasmid encodes for the fusion of an AD (VP64) and DBD (Gal4) with KRas (G12D), and another fusion construct of AD (VP64) and DBD (LexA) with KRas, and the E3 ubiquitin ligase Cereblon (CRL4-CRBN). The protein fusion sequences are tagged with either FLAG, MYC or HA. The plasmid further includes yeast replication and selection markers (TRP1 and CEN). The plasmid also has sites for integration into the genome at a specified locus.
The Saccharomyces cerevisiae is co-transformed with a selection and library plasmid for the expression of a randomized peptide library, NNK 20-mer sequences. The selection plasmid is driven by a strong promoter, ADH1. The selection and library plasmid also comprises a sequence that encodes a HIS tag.
The selection and library plasmid additionally comprises a LexAop sequence, which induces ‘death agents’ (cytotoxic reporter expression) when bound by a functional transcriptional factor that is formed by Gal4—KRas (G12D)—VP64 fusion protein. The selection and library plasmid also contains a positive selection marker, ADE2 which is under control of LexA—KRas—VP64 fusion protein and leading to expression of the positive selection marker when the fusion protein is expressed. The plasmid further includes yeast replication and selection markers (TRP1 and CEN).
The screen is performed by mating the strains in a batch to result in a diploid strain, which carries all the markers, the target protein, the E3 ligase, the positive selection, the death agents, and the peptide. This batch culture is then propagated on solid medium, which enable selection of all the system components (media lacking two nutritional components) and induce expression of any inducible component with Gal.
Surviving colonies constitute cells with degraded KRas (G12D), that can no longer trigger the death cascade induced by the encoded death agents, the degradation of which has been facilitated by a peptide bridging to Cereblon. The same cells also express WT KRas that was not targeted and is driving positive selection to enable survival.
The peptide sequence that is able to selectively degrade KRas (G12D) is obtained by DNA sequencing the peptide-encoding region of the selection and library plasmid in each surviving colony.
To confirm specificity, the inducible marker is used to inactivate the production of the E3 ligase and confirm specificity. The plasmid is then isolated and re-transformed into a fresh parental strain to confirm specificity.
Biochemical fractionation of the viable strain that contained the target, E3 ligase, peptide, selection marker, and death agent is followed by pull-down experiments to confirm an interaction between the peptide sequence and either protein using the encoded tags.
An alternative example can be made by switching LexA with Gal4. In another alternative example, fusion proteins in either construct are driven by an inducible promoter, GAL1, instead of ADH1 promoter. In another example, yeast selection marker 2 um is included in the target and E3 ligase integration plasmid and selection and library plasmid, instead of CEN. Similarly, yeast selection marker LEU2 can be used alternatively in another example. In yet another example, the N-terminus of the peptide translated from the selection and library plasmid can alternatively be glycine, alanine, serine, threonine, valine, or proline. In other examples, the genetic reporter in the confirmation plasmid is HIS3 or URA3, in place of ADE2. Either mating types of Saccharomyces cerevisiae haploid state can be used as background strain in alternative examples. In other examples, the library of peptides can be expressed from scaffolds that enable post translational modifications. In other examples, background strains also express the enzymes for the cyclization and methylation of peptides like lanthipeptides maturation enzymes from Lactococcus lactis (LanB, LanC, LanM, LanP), patellamide biosynthesis factors from cyanobacteria (PatD, PatG), butelase 1 from Clitoria ternatea, and GmPOPB from Galerina marginata or other species.
In this example, the target bait is operationally linked to a positive selection marker that enables growth in the absence of an essential nutrient (schematic as shown in
In this example, the target bait was operationally linked to a ‘Death Agent’ negative selection marker that prevents cell growth when expressed as also described in
In another example, cells expressing a heterologous E3 ligase, in this case TIR1, were assayed for survival to discover bridging agents that can bridge TIR1 to the bait and lead to degradation, thereby enabling cell growth (schematic shown in
In yet another example, cells expressing a heterologous E3 ligase, in this case COI1b, were assayed for survival to discover bridging agents that can bridge COI1b to the bait and lead to degradation, thereby enabling cell growth (as shown in
This application is a continuation application of International Application No. PCT/US20/33089, filed on May 15, 2020, which claims the benefit of U.S. Provisional Application No. 62/848,509, filed on May 15, 2019 and U.S. Provisional Application No. 62/854,273, filed on May 29, 2019, which are incorporated herein by reference in their entirety.
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| Number | Date | Country | |
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| 62848509 | May 2019 | US | |
| 62854273 | May 2019 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/US2020/033089 | May 2020 | US |
| Child | 17317798 | US |
