Patent Application
20240398964
The present invention relates to a peptide for penetrating the blood-brain barrier and use thereof, and more specifically, a peptide for penetrating the blood-brain barrier, or a conjugate in which a drug, such as an antibody, a protein or a therapeutic nucleic acid, is conjugated to the peptide; and use thereof for the treatment or prevention of brain diseases or brain tumors.
The blood-brain barrier (BBB) is the most powerful biological barrier, a defense system that helps maintain the brain's complex physiology by selectively allowing only substances in the blood that are essential for maintaining brain function to pass through. The BBB is composed of capillaries formed from brain endothelial cells and the astrocytes and pericytes that surround them, each of which contributes to the strength of the BBB's unique biofilm. Unlike endothelial cells in other organs, brain endothelial cells have tight junctions that strongly inhibit the transcellular passage of 300 Da or more hydrophilic substances, which is known as physical barrier function. In addition, polarized endothelial cells have various types of multidrug efflux pumps, such as P-glycoprotein, MRP1, MRP4 and BCRP, which bind hydrophobic drugs and prevent drug penetration into brain tissue, which is called metabolic barrier function. Astrocytes extend their protrusions toward established brain capillaries to form astrocytic endfeet that cover most of the surface of the vessel, and it has recently been suggested that these endfeet play a pivotal role in maintaining the biological barrier by defending against harmful factors to the BBB.
Therefore, neurological drugs, such as drugs with large molecular weight that need to work inside the brain or drugs with small molecule weight with low brain penetration, cannot cross the blood-brain barrier (BBB).
Previous technologies have utilized the transcytosis pathway mediated by endogenous receptors expressed on the endothelium of brain capillaries, to cross the blood-brain barrier. Antibodies or peptides against transferrin receptors were designed based on the fact that many transferrin receptors are present on the surface of brain endothelial cells. Antibodies that bind to transferrin receptors cannot directly cross the cell membrane and can enter the brain endothelial cells by endocytosis. They have a limitation that, once entering into the cerebrovascular cells by endocytosis, they form endosomes, and if they cannot escape from the endosomes, they are transferred to the lysosome for degradation.
Brain endothelial cells also contain receptors for low density lipoprotein receptor (LDLR)-related proteins (LRPs), in addition to transferrin. The low density lipoprotein receptor-related proteins receptor endocytoses LDL particles, making them permeable to the BBB. These LRPs receptors do not undergo lysosomal translocation and degradation, and are favorable receptors for the delivery of drugs used to treat neurodegenerative diseases.
Previous studies have shown that IgG injected into the bloodstream permeates the CNS compartment at a very low rate (about 0.1%) [Felgenhauer, Klin. Wschr. 52:1158-1164 (1974)], resulting in very limited pharmacokinetic effects within the CNS. Therefore, there is a need for delivery systems for neurological drugs that can cross the BBB and effectively transport the drug to the brain.
Accordingly, the inventors of the present invention have prepared a peptide for penetrating the blood-brain barrier (BBB) in which a cell-permeable peptide is linked to a transferrin receptor binding peptide or a low density lipoprotein receptor-related protein receptor binding peptide, and have found that the prepared peptide can directly cross the cell membrane of a brain endothelial cell without relying on endocytosis, and the peptide-drug complex for penetrating the blood-brain barrier in which a drug, such as an antibody, protein, or therapeutic nucleic acid, is conjugated to the peptide for penetrating the blood-brain barrier is effectively delivered to the brain parenchyma, and has the effect of treating brain tumors, and completed the present invention.
The above information in this Related Art is intended solely to enhance the understanding of the background of the present invention and may not include information that constitutes prior arts known to one having ordinary skill in the art.
It is an object of the present invention to provide a peptide for penetrating the blood-brain barrier (BBB) to effectively deliver drugs for the treatment of brain diseases or brain tumors into the brain parenchyma.
Another object of the present invention is to provide a peptide-drug complex for penetrating the blood-brain barrier in which a drug is conjugated to the peptide for penetrating the blood-brain barrier.
Another object of the present invention is to provide a pharmaceutical composition for treating or preventing brain diseases or brain tumors, comprising the peptide-drug complex for penetrating the blood-brain barrier.
Another object of the present invention is to provide a method of preventing or treating brain diseases or brain tumors, comprising the step of administering the complex, use of the complex for preventing or treating brain diseases or brain tumors, and use of the complex for manufacturing a medicament for preventing or treating brain diseases or brain tumors.
To accomplish the above objectives, the present invention provides a peptide for penetrating the blood-brain barrier (BBB), comprising a brain endothelial cell surface protein-binding peptide and a cell-permeable peptide.
The present invention also provides a peptide-drug complex for penetrating the blood-brain barrier, wherein a drug is conjugated to the peptide for penetrating the blood-brain barrier.
The present invention also provides a nucleic acid encoding the complex.
The present invention also provides a recombinant vector into which the nucleic acid is introduced.
The present invention also provides a recombinant cell into which the nucleic acid or the recombinant vector is introduced.
The present invention also provides a method of producing a peptide-drug complex for penetrating the blood-brain barrier, comprising (a) culturing the recombinant cells to express the peptide-drug complex for penetrating the blood-brain barrier; and (b) recovering the expressed the peptide-drug complex for penetrating the blood-brain barrier.
The present invention also provides a pharmaceutical composition for treating or preventing brain diseases or brain tumors, comprising the peptide-drug complex for penetrating the blood-brain barrier.
The present invention also provides a method of preventing or treating brain diseases or brain tumors, comprising the step of administering the complex, use of the complex for preventing or treating brain diseases or brain tumors, and use of the complex for manufacturing a medicament for preventing or treating brain diseases or brain tumors.
Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by a person skilled in the art. In general, the nomenclature used herein is well known and in common use in the art.
In the present invention, a peptide capable of binding to transferrin receptors using phage display techniques instead of antibodies was designed to prevent the endosomal to lysosomal transfer of substances permeated into brain endothelial cells. This transferrin receptor binding peptide is characterized by binding to a different part of the transferrin receptor than the part where the transferrin binds to the transferrin receptor. Furthermore, low density lipoprotein receptor (LDLR)-related proteins (LRPs) receptor binding peptides have been devised.
By linking a transferrin receptor-binding peptide or low density lipoprotein receptor-related protein receptor binding peptide with a peptide with cell-penetrating function, the inventors of the subject invention have developed a peptide for penetrating the blood-brain barrier (BBB) that can directly penetrate the cell membrane of brain endothelial cells without relying on endocytosis, and named NIPEP-TPP-BBB shuttle (NIBEC Peptide-Target Tissue Penetrating Property-BBB shuttle).
In addition, drugs such as antibodies, proteins, or therapeutic nucleic acids were attached to the N-terminus of the peptide for penetrating the blood-brain barrier using gene expression method or chemical coupling method to deliver it to the brain parenchyma when intravenously injected into mice, and tumor cells were reduced when administered to animals with glioblastoma.
Thus, in one aspect, the present invention relates to a peptide for penetrating the blood-brain barrier (BBB) comprising a brain endothelial cell surface protein-binding peptide and a cell-permeable peptide.
In the present invention, the brain endothelial cell surface protein may be characterized as being a transferrin receptor or a low density lipoprotein receptor-related protein (LRP) receptor. Thus, the peptide for penetrating the blood-brain barrier may be characterized by a peptide capable of binding to a transferrin receptor or a peptide capable of binding to a low density lipoprotein receptor (LDLR)-related protein receptor is linked to a cell-permeable peptide.
In the present invention, the transferrin receptor binding peptide may be represented by an amino acid sequence of any one of SEQ ID NO: 1 to SEQ ID NO: 4.
In the present invention, the term “transferrin receptor” refers to a specific receptor on transferrin for the entry of iron into a cell, comprising a homodimer having polypeptide chains with a molecular weight of 95,000 Da, each chain having one molecule of transferrin in which iron ions are bound.
In the present invention, the term “transferrin” refers to a type of glycoprotein, an iron-transporting protein, wherein β-globulin binds to two molecules of divalent iron ion absorbed to serum, and iron required for cell proliferation or hemoglobin production is delivered, and 99% or more of the iron in serum is bound to transferrin.
In the present invention, the low density lipoprotein receptor-related protein receptor binding peptide may be represented by an amino acid sequence of SEQ ID NO: 5 or SEQ ID NO: 6.
In the present invention, the term “low density lipoprotein receptor-related protein receptor (LRP receptor)” refers to a cell membrane protein known to be highly expressed in brain endothelial cells, small intestinal epithelium, and the like, and functions to endocytose LDL particles and permeabilize the BBB.
In the the present invention, the term “low density lipoprotein receptor (LDLR)-related proteins (LRPs)” refers to glycoproteins of 600 kDa belonging to the LDL receptor gene family, which are expressed in a number of tissues, including hepatocytes, adipocytes, fibroblasts, macrophages and neurons of the central nervous system (Herz J., et al., EMBO Journal, 20, 4119-27 (1988)), with high concentrations in the liver and brain. The function of LRP in the central nervous system is particularly important in the cerebellum, cerebral cortex, hippocampus, and brainstem (Qian Z., et al., Nature, 361, 453-457 (1993).
In the present invention, the cell-permeable peptide may be represented by an amino acid sequence of any one of SEQ ID NO: 7 to SEQ ID NO: 10.
In the present invention, the cell-permeable peptide may be characterized by being directly linked to the N-terminus, C-terminus, or both sides of the N-terminus and C-terminus of the transferrin receptor binding peptide or low density lipoprotein receptor-related protein receptor binding peptide, but is not limited thereto.
In the present invention, the peptide for penetrating the blood-brain barrier can be characterized by being represented by an amino acid sequence of any one of SEQ ID NO: 11 to SEQ ID NO: 58 (Table 1).
In the present invention, the brain endothelial cell surface protein-binding peptide and cell-permeable peptide may be linked via a spacer comprising 2 to 10 amino acids G and 1 to 5 amino acids S.
In another aspect, the present invention relates to a peptide for penetrating the blood-brain barrier-drug complex, wherein a drug is conjugated to the peptide for penetrating the blood-brain barrier.
In the present invention, the peptide and drug for penetrating the blood-brain barrier are connected by a linker, but are not limited thereto.
In the present invention, the drug may be an antibody, a protein or a therapeutic nucleic acid, wherein the antibody may be an antibody that inhibits a protein that causes a brain disease, and the protein may be a growth factor associated with neurons, but is not limited thereto.
In the present invention, the protein may be selected from the group consisting of brain-derived neurotrophic factor (BDNF), nerve growth factor (NGF), neurotrophin-4/5, fibroblast growth factor (FGF)-2 and other FGFs, neurotrophin (NT)-3, erythropoietin (EPO), epidermal growth factor (EGF), transforming growth factor (TGF)-alpha, TGF-beta, vascular endothelial growth factor (VEGF), glial cell-derived neurotrophic factor (GDNF), neurturin, platelet-derived growth factor (PDGF), herregulin, neuregulin, artemisin, persepsin, interleukin, glial cell line-derived growth factor (GFR), granulocyte-colony stimulating factor (CSF), granulocyte-macrophage-CSF, and stem cell factor (SCF).
In the present invention, the antibody can be represented by an amino acid sequence of SEQ ID NO: 59 and has therapeutic efficacy in glioblastoma.
MAWVWTLLFLMAAAQSIQAEWIKQRPGQGLEWIGVIHPGNGGTNY
SHHHHHHHHH
In the present invention, a peptide-drug complex for penetrating the blood-brain barrier in which an antibody is conjugated to the peptide for penetrating the blood-brain barrier can be prepared by a gene expression method or a chemical conjugation method, but the preparation method is not limited thereto.
For preparing a peptide-drug complex for penetrating the blood-brain barrier by gene expression method, a vector expressed together with (i) an antibody capable of inhibiting glioblastoma and (ii) a peptide for penetrating the blood-brain barrier can be utilized. In the present invention, the pET vector was used for expression in E. coli, and the pcDNA3.1-TOPO and pcDNA3.4-TOPO vectors were used for expression in mammalian cells.
In this case, a linker sequence may be further included between the antibody and the peptide for penetrating the blood-brain barrier for expression, and preferably, the linker may be, but is not limited to, CGGGG.
In the present invention, a therapeutic antibody can be expressed in a gene, purified, and chemically coupled to a peptide for penetrating the blood-brain barrier.
In the present invention, a peptide-drug complex for penetrating the blood-brain barrier of a therapeutic antibody and a peptide for penetrating the blood brain barrier, wherein a transferrin receptor selected from the group consisting of SEQ ID NO: 1 to SEQ ID NO: 4, or a low density lipoprotein receptor-related protein receptor binding peptide of SEQ ID NO: 5 or 6, and a cell-permeable peptide selected from the group consisting of SEQ ID NO: 7 to SEQ ID NO: 10 are chemically linked to a cysteine at the C-terminus of the antibody of SEQ ID NO: 59 or to a sugar in the Fc region. This is illustrated in the schematic of
The peptide for penetrating the blood-brain barrier may be chemically linked to the antibody by linkers and crosslinkers. The linker may be any one that can provide space to form a functional structure. For example, the linker may be a peptidic linker of natural and/or synthetic origin. Peptidic linkers of natural and/or synthetic origin may be composed of amino acid chains of 1 to 50 amino acids, and may comprise repeating amino acid sequences of naturally occurring polypeptides, such as polypeptides with hinge functions. In another aspect, the peptidic linker amino acid sequence may be a synthetic linker amino acid sequence specified to have rich glycine, glutamine, and/or serine residues. These residues may be arranged in small repeating units of, for example, five or fewer amino acids, and the small repeating units may be repeated and arranged to form a multimer unit. At the amino- and/or carboxy-terminus of the multimer unit, six or fewer additional naturally occurring amino acids may be added. Other synthetic peptidic linkers may be of a single amino acid composition with 10 to 20 repeats, and no more than 6 additional naturally occurring amino acids at the amino- and/or carboxy-termini. Meanwhile, the linker may be a chemically modified form of the amino acid, for example, but not limited to, in the form of Fmoc-6-aminohexanoic acid conjugated with Fmoc-(9-Fluorenylmethoxycarbonyl) as a blocking group.
In some aspects according to the present invention, a sulfhydryl group of cysteine located at the N terminus of the peptide for penetrating the blood-brain barrier can be linked to an amine group of lysine in the exposed portion of the three-dimensional structure of SEQ ID NO: 59.
In this case, the crosslinkers that can be used may be, but is not limited to, 1,4-bis-maleimidobutane (BMB), 1,11-bis-maleimidotetraethyleneglycol (BM[PEO]4), 1-ethyl-3-[3-dimethyl aminopropyl] carbodiimide hydrochloride (EDC), succinimidyl-4-[N-maleimidomethylcyclohexane-1-carboxy-[6-amidocaproate] (SMCC) and its sulfonated salt (sulfo-SMCC), succimidyl 6-[3-(2-pyridyldithio)-ropionamido] hexanoate] (succimidyl 6-[3-(2-pyridyldithio)-ropionamido] hexanoate (SPDP) and its sulfonated salt (sulfo-SPDP), m-maleimidobenzoyl-N-hydroxysuccinimide ester (MBS) and its sulfonated salts (sulfo-MBS), or succimidyl [4-(p-maleimidophenyl) butyrate] (SMPB) and its sulfonated salts (sulfo-SMPB).
In the present invention, a method of preparing a peptide-drug complex for penetrating the blood-brain barrier using the above chemical coupling method comprises the following steps:
In the present invention, the therapeutic nucleic acid may be selected from the group consisting of DNA, siRNA, miRNA and mRNA, and preferably the therapeutic nucleic acid has the function of inhibiting or increasing the expression of a target gene. The siRNA may have a base sequence complementary to a base sequence encoding an oncogenic protein, or a protein causing brain disease.
In one aspect of the present invention, expression of mutant KRAS is inhibited using siRNA against mutant KRAS, wherein the siRNA may be represented by SEQ ID NO: 60 or SEQ ID NO: 61.
KRAS siRNA Sequence:
In the present invention, the siRNA may be in its natural form or a chemically modified form of siRNA.
The present invention may be characterized in that the therapeutic nucleic acid is reacted with a cationic peptide, cationic polymer, or RNA binding peptide to prepare a primary complex, and then the primary complex is reacted with an anionic amino acid or an anionic polymer; and the peptide for penetrating the blood-brain barrier linked with a spacer to form a nanoparticle.
In the present invention, the cationic peptide is represented by the amino acid sequence of SEQ ID NO: 9, the cationic polymer is poly-L-lysine, polyethylene imine or chitosan, and the RNA binding peptide is represented by the amino acid sequence of any one of SEQ ID NO: 62 to SEQ ID NO: 67, the anionic amino acid is glutamic acid or aspartic acid, the anionic polymer is heparin or hyaluronic acid, and the spacer is 5 to 10 glycines, but is not limited thereto.
To permeabilize the therapeutic nucleic acid across the blood brain barrier, an RNA binding peptide may be introduced in addition to the peptide for penetrating the blood-brain barrier, wherein the RNA binding peptide is represented by an amino acid sequence of any one of SEQ ID NO: 62 to SEQ ID NO: 67.
The peptide of SEQ ID NO: 62 to SEQ ID NO: 67 can be used in conjunction with, but not limited to, the N-terminus of the complex of SEQ ID NO: 11 to SEQ ID NO: 58.
In the present invention, the complex of siRNA and a peptide for penetrating the blood-brain barrier may be characterized in that at least one transferrin receptor binding peptide selected from the group consisting of SEQ ID NO: 1 to SEQ ID NO: 4, or a low density lipoprotein receptor-related protein receptor binding peptide of SEQ ID NO: 5 or SEQ ID NO: 6; at least one cell-permeable peptide selected from the group consisting of SEQ ID NO: 7 to SEQ ID NO: 10; and an RNA binding peptide consisting of SEQ ID NO: 62 to SEQ ID NO: 67 and siRNA of SEQ ID NO: 60 or SEQ ID NO: 61 form a complex by self-assembly. The complex forms nano-sized particles, which may be characterized as having a size of 10-200 nm.
In the present invention, the complex of siRNA and a peptide for penetrating the blood-brain barrier can be prepared in two steps. 1) The siRNA is first reacted with a cationic peptide or cationic polymer. The cationic peptide can be a peptide of SEQ ID NO: 9, and the cationic polymer can be poly-L-lysine, polyethylene imine, or chitosan. 2) The next step is to conjugate the peptide for penetrating the blood-brain barrier to the anionic amino acid or anionic polymer. In this case, the complex of peptide for penetrating the blood-brain barrier, spacer and anionic amino acid may be represented by an amino acid sequence of any one of SEQ ID NO: 68 to SEQ ID NO: 85.
In addition, anionic polymers such as heparin or hyaluronic acid can be used instead of the anionic amino acids glutamic acid or aspartic acid.
By self-assembly, siRNA is first reacted with a peptide of SEQ ID NO: 9, and then a peptide for penetrating the blood-brain barrier is combined, and the complex forms nano-sized particles having a size of 10-200 nm.
In the present invention, a method of forming a complex of therapeutic nucleic acids, including siRNA, by the self-assembly comprises the following steps:
In another aspect, the present invention relates to a nucleic acid encoding the peptide-drug complex for penetrating the blood-brain barrier.
In another aspect, the present invention relates to a recombinant vector in which the nucleic acid is introduced.
In the present invention, the vector may be, but is not limited to, a pET vector, pcDNA 3.4, pcDNA3.1, pcDNA3.1-TOPO, pcDNA3.4-TOPO, or pSecTag vector, and preferably a pET vector or a pcDNA3.1-TOPO, pcDNA3.4-TOPO vector.
In another aspect, the present invention relates to a recombinant cell into which the nucleic acid or the recombinant vector is introduced.
In the present invention, the recombinant cell may be E. coli or mammalian cells, but is not limited thereto.
In the present invention, the mammalian cell line can be, but is not limited to, Chinese hamster ovarian cell line (CHO), human embryonic kidney cell line (HEK293), and human embryonic kidney cell line (HEK293).
In another aspect, the present invention relates to a method of preparing the peptide-drug complex for penetrating the blood-brain barrier, comprising the following steps:
Antibodies that inhibit glioblastoma or siRNAs that inhibit mutations, which are representative antibodies that inhibit brain diseases, do not have a significant therapeutic effect because they are unable to penetrate the blood-brain barrier. On the other hand, in other embodiments of the present invention, when the brain delivery effect or tumor proliferation inhibition effect of antibodies or siRNAs conjugated with peptides that can penetrate the blood-brain barrier was checked, both in vitro and in animal experiments, it was found that the proliferation of the corresponding tumor cells was significantly inhibited.
Accordingly, in another aspect, the present invention relates to a pharmaceutical composition for treating or preventing brain diseases or brain tumors comprising the peptide-drug complex for penetrating the blood-brain barrier.
In another aspect, the present invention relates to a method of preventing or treating brain diseases or brain tumors, comprising the step of administering a peptide-drug complex for penetrating the blood-brain barrier.
In another aspect, the present invention relates to the use of the peptide-drug complex for penetrating the blood-brain barrier for the prevention or treatment of brain diseases or brain tumors.
In another aspect, the present invention relates to the use of the peptide-drug complex for penetrating the blood-brain barrier for the preparation of an agent for the prevention or treatment of brain diseases or brain tumors.
In the present invention, antibodies or therapeutic nucleic acid substances that can be used to treat other brain diseases in addition to brain tumor inhibition can be combined with peptides for penetrating the blood-brain barrier.
In the present invention, the brain disease may be selected from the group consisting of encephalitis, Parkinson's disease, epilepsy, Huntington's disease, Alzheimer's disease, Lou Gehrig's disease, Pick's disease, epilepsy, Creutzfeldt-Jakob disease, progressive supranuclear palsy, spinocerebellar degeneration, cerebellar atrophy, multiple sclerosis, senile dementia caused by the loss of nerve cells, stroke, amnesia, depression, and post-traumatic stress disorder.
In the present invention, the brain tumor may be selected from the group consisting of glioma, glioblastoma multiforme, meningioma, astrocytoma, acoustic neuroma, chondroma, rare glioblastoma, medulloblastoma, ganglioneuroma, schwannoma, neurofibroma, neuroblastoma, and epidural, intramedullary or intrathecal tumors.
In the present invention, a single dose of the peptide-drug complex for penetrating the blood-brain barrier may be 1 μg/kg to 100 mg/kg, preferably 5 μg/kg to 50 mg/kg, and may be characterized by administration once daily or 1-3 times per week, but the dose and dosing interval are not limited thereto.
In the present invention, the pharmaceutical composition may be formulated in any one of the dosage forms selected from the group consisting of, but not limited to, liquids (e.g., for injection) such as injectables, oral preparations, aqueous solutions or emulsions, capsules, granules, tablets, and mucosal delivery agents. These formulations may be prepared by conventional methods used in the art for formulation or by methods disclosed in Remington's Pharmaceutical Science (latest edition), Mack Publishing Company, Easton PA, and may be formulated in various formulations for different conditions or based on ingredients.
In the present invention, the pharmaceutical composition of the present invention may further comprise one or more pharmaceutically acceptable carriers in addition to the complex of antibody or siRNA conjugated to the peptide for penetrating the blood-brain barrier. The pharmaceutically acceptable carrier may be one or more selected from the group consisting of, but not limited to, saline, sterile water, Ringer's solution, buffered saline, dextrose solution, maltodextrin solution, glycerol, and ethanol.
The pharmaceutical composition of the present invention may further contain pharmaceutically acceptable auxiliaries as required. The adjuvant may be one or more selected from the group consisting of, but not limited to, excipients, diluents, dispersants, buffers, antimicrobial preservatives, bacteriostatic agents, surfactants, binders, lubricants, antioxidants, thickeners, and viscosity modifiers.
The pharmaceutical composition according to the present invention may be administered orally or parenterally (e.g., intravenously, subcutaneously, intraperitoneally or topically), depending on the intended method, and the dosage may be varied according to the expert's opinion, depending on the patient's weight, age, gender, health status, diet, time of administration, method of administration, excretion rate, and severity of the disease.
The present invention is described in more detail by providing the following examples. These examples are intended solely to illustrate the present invention, and it would be apparent to one of ordinary skill in the art that the scope of the present invention is not to be construed as limited by these examples.
Amino acids and reagents required for synthesis were purchased from GL biochem and Sigma-Aldirich. The peptide was synthesized by F-moc solid-phase chemical synthesis from the C-terminus using the peptide synthesis method. That is, Rink resin with Fmoc-(9-Fluorenylmethoxycarbonyl) as the blocking group (0.075 mmol/g, 100˜200 mesh, 1% DVB crosslinking) was synthesized by adding 50 mg of rink resin in the synthesizer, followed by swelling of the resin with DMF, and then using a 20% piperidine/DMF solution for removal of the Fmoc-group. Starting from the C-terminus, in sequence, 0.5 M amino acid solution (solvent: dimethylformamide, DMF), 1.0 M DIPEA (solvent: dimethylformamide & n-methylpyrrolidone, DMF & NMP), and 0.5 M HBTU (solvent: dimethylformamide, DMF) were added in 5, 10, and 5 equivalents, respectively, and reacted under a nitrogen stream for 1-2 hours. After each of the above deprotection and coupling steps, washing was conducted twice with DMF and isopropanol. Deprotection was also performed after coupling the last amino acid to remove the Fmoc-group. After removing the F-moc protecting group of the last amino acid at the N-terminus, the synthesis proceeded by adding DIPEA (10 equivalents), HBTU (5 equivalents), and palmitic acid (5 equivalents) in the presence of DMF. The reaction proceeded until a negative result was obtained using the Kaiser test solution for measuring the reaction time, and after the end of the reaction, the resin was washed with DMF and MeOH and dried in a vacuum oven. Trifluoroacetic acid (TFA) cleavage cocktail was added at a ratio of 20 ml per gram of resin and shaken for 3 hours to separate the resin and the peptide dissolved cocktail by filtering. The filtered solution was removed using a rotary evaporator and then cold ether was added or an excess of cold ether was added directly to the TFA cocktail solution in which the peptide was dissolved to crystallize the peptide into a solid phase, and then separated by centrifugation. The TFA cocktail was then completely removed by washing with ether several times and centrifugation. The resulting peptides were dissolved in distilled water and lyophilized. After lyophilization, they were separated and purified by high-performance liquid chromatography (Shimadzu, Japan). The analysis was performed using a 4.6 mm diameter C18 column with 0.1% TFA/H2O and 0.092% TFA/acetonitrile at a flow rate of 1 ml/min with a gradient of 0 to 60% for 30 min, and the wavelength of the UV detector was 220 nm. Purification was performed using a 2.2 cm diameter column at a flow rate of 20 ml/min with the same solvent and detection wavelength. The molecular weight of the purified peptide was confirmed by mass spectrometry.
1 mg of Alexa Fluor™ 680 NHS Ester (=Cy5.5-NHS ester, Invitrogen, A37567) and 2 mg of the synthesized peptide were dissolved in 0.1 ml of DMF. 0.05 ml pyridine was added and the reaction was performed on a 50° C. heat block for 15 min. 0.7 ml ethyl acetate was added to form a precipitate, and then centrifuged at 10,000 rpm for 2 minutes. The supernatant was removed, washed twice with 0.7 ml of ethyl acetate in the same way, and dried in air.
The linker CGGGG was introduced at the N-terminus of the peptide for penetrating the blood-brain barrier (SEQ ID NO: 41) prepared using the method of Example 1, and the antibody of SEQ ID NO: 59 was chemically conjugated. 1.02 mg of antibody of SEQ ID NO: 59 was dissolved in 1 mL of PBS buffer (pH 8.3). 2.12 mg of SPDP (succinimidyl 3-(2-pyridyldithio) propionate, ThermoFisher, 21857) was dissolved in 120 μL DMSO (Dimethyl sulfoxide). 40 μL of SMCC solution was added thereto, and the reaction was repeated three times by shading for 1 hour. At the end of the reaction, desalting was performed using a PD-10 Desalting Column (GE healthcare) and 3.5 mL of pyridyldithiol activated antibody was obtained. 2.5 mg of SEQ ID NO: 42 solution was mixed in 300 μL of tertiary purified water and adjusted to pH 8.3 using 1 M tris buffer (pH=9). After shading, the reaction was performed overnight with mixing at 4° C. The antibody conjugated with a peptide for penetrating the blood brain barrier was purified by FPLC (Akta Pure, GE healthcare) using a heparin column (HiTrap, GE Healthcare).
For animal cell expression, the gene sequence, wherein the peptide for penetrating the blood brain barrier of SEQ ID NO: 15 to SEQ ID NO: 18 was conjugated to the C term of the antibody of SEQ ID NO: 59 in the pcDNA3.4-TOPO vector, was synthesized.
MAWVWTLLFLMAAAQSIQAEWIKQRPGQGLEWIGVIHPGNGGTNY
MAWVWTLLFLMAAAQSIQAEWIKQRPGQGLEWIGVIHPGNGGTNY
LLGLDSTGGSGGSHHHHHH
MAWVWTLLFLMAAAQSIQAEWIKQRPGQGLEWIGVIHPGNGGTNY
PNPLLGLDSTGGSGGSHHHHHH
MAWVWTLLFLMAAAQSIQAEWIKQRPGQGLEWIGVIHPGNGGTN
KPIPNPLLGLDSTGGSGGSHHHHHH
By cutting pcDNA3.1-TOPO or pcDNA3.4-TOPO with EcoR I and BamH I, a KRAS mutant scFv gene fragment with 900-960 bp was recovered by agarose electro elution. To insert it into a pcDNA3.1-TOPO or pcDNA3.4-TOPO vector, the gene was amplified by PCR, and BamH I and EcoR I restriction enzyme sites were synthesized at the same time. The respective truncated vectors and inserts were mixed in a ratio of 4 μl to 4 μl, respectively, and reacted for 16-18 hours at 4° C. using T4 DNA ligase in ligation buffer solution composed of Tris-HCl 500 mM, MgCl2 100 mM, DTT 200 mM, and ATP 10 mM.
The prepared vector was transfected into the Chinese hamster ovary cell line Expi-CHO-S. The Chinese hamster ovary cell line ExpiCHO-S was obtained from Thermo Fisher Scientific (USA) and cultured in ExpiCHO Expression medium medium (GIBCO, USA). The ExpiCHO-S cell line (3×108 cells) was then placed in 50 mL of culture medium in 250 ml disposable Erlenmeyer flasks. 2 mL of Opti-MEM containing 50 μg of plasmid was mixed with 160 μL of ExpiFectamine CHO Reagent (Gibco, Cat #A20130) diluted in 1.84 mL of Opti-MEM and it was stop-reacted for 5 minutes at room temperature, then evenly spotted onto the prepared Chinese hamster ovary cells, and incubated in 8% CO2 thermostat at 37° C., for 18 hours, and then 300 μL of ExpiCHO enhancer and 12 mL of ExpiCHO Feed were added and incubated for 5 days. Six days after transfection, the culture medium was collected, sterilized, and purified using FPLC. Columns were separately purified using nickel chromatography (HisTrap™ excel, GE healthcare), pre-wetting the nickel column with buffer at [20 mM sodium phosphate, 0.5 M NaCl, pH 7.4] to equalize it, and then applying the medium. After washing with the buffer containing 25 mM of imidazole, proteins were separated by increasing the imidazole to 125 mM. The isolated proteins were pooled and stored by desalting to remove imidazole.
Cy5.5 labeled SEQ ID NO: 17 peptide for penetrating the blood-brain barrier, Cy5.5 labeled SEQ ID NO: 59 antibody, and the complex of Cy5.5-labeled SEQ ID NO: 17 peptide for penetrating the blood-brain barrier and SEQ ID NO: 59 antibody were injected intravenously at 4 mg/kg each to hairless mouse (SKH-1, female, 6 weeks old, OrientBio), and fluorescence in each organ (brain, liver, lung, spleen, kidney, heart) was measured at excitation: 685 nm and emission: 706 nm using IVIS (Perkin Elmer). In addition, three-dimensional images of the brain alone were measured using Optix MX3 (ART Advanced Research Technologies Inc.).
As shown in
The control cell permeability peptide (TAT) and antibody of SEQ ID NO: 59 were prepared in the same manner as the expression method in Example 2 and labeled with cy5.5. The complex of the peptide for penetrating the blood-brain barrier of SEQ ID NO: 41 in which CGGGG was introduced in N term and the antibody of SEQ ID NO: 59 prepared in Example 2 was labeled labeled with Cy5.5. The antibody of SEQ ID NO: 59 was labeled with Cy5.5 and injected intravenously into hairless mouse (SKH-1, female, 6 weeks old, OrientBio) at 10 mg/kg each. Concentrations in brain and blood were measured at excitation: 685 nm and emission: 706 nm using IVIS (Perkin Elmer) until day 24, and the results are shown in
When administered alone, the antibody was cleared from the blood within 12 days. Both the antibody linked to TAT and the antibody linked to the peptide for penetrating the blood-brain barrier of SEQ ID NO: 41 were retained up to 24 days. However, the blood levels of the complex of the peptide for penetrating the blood-brain barrier of SEQ ID NO: 41 and the antibody were higher.
In addition, no fluorescence was measured in brain tissue when the antibody was administered alone. With the TAT-linked antibody, 2.4% of the initial dose of fluorescence was measured in brain tissue 4 days after intravenous injection. The complex of the peptide for penetrating the blood-brain barrier of SEQ ID NO: 41 and the antibody of SEQ ID NO: 59 was measured approximately 7% of the initial dose in brain tissue 4 days after intravenous injection. This demonstrates that the complex of the peptide for penetrating the blood-brain barrier of SEQ ID NO: 41 and the antibody of SEQ ID NO: 59 are more efficient in brain delivery.
Using a brain tumor animal model, the ability of the complex of the peptide for penetrating the blood-brain barrier and antibody to penetrate the brain, inhibit brain tumors, and be distributed in the brain parenchyma was measured. Specifically, U87MG-Luc 2 (ATCC, HTB-14-LUC2™) cells, a luciferase-expressing U87MG glioblastoma, were cultured in DMEM medium supplemented with 10% FBS and 1% antibiotics. Nude 5- to 7-week-old mouse (Orient Bio) was anesthetized with isoflurane and immobilized using ear bars inside a stereotaxic instrument. After incising the scalp at the surgical site, a hole was made using a sterile drill 2 mm to the right to and 2 mm under the bregma. Then, 1.0×105/10 μL U87MG-Luc-2 cells were injected through the above hole with a 26G Hamilton syringe (1 μl/min), and after injection, the hole was closed with bone wax and sutured to close the scalp. The proliferation of transplanted glioblastoma was obtained by injecting D-luciferin potassium (15 mg/mL dissolved in PBS, sigma), a substrate of luciferase, at 150 mg/kg, to a mouse, and sacrificing it after 10 min, and measuring the bioluminescence using IVIS (Perkin Elmer), and the results are shown in
Starting 4 days after glioblastoma transplantation, 1 mg/kg of the complex of CGGGG-SEQ ID NO: 41 peptide for penetrating the blood-brain barrier and SEQ ID NO: 59 antibody and 1 mg/kg SEQ ID NO: 59 antibody were injected intravenously. The administration interval between doses was every 3 days for a total of 4 doses for 16 days.
The complex of a peptide for penetrating the blood-brain barrier of CGGGG-SEQ ID NO: 41 labeled with cy5.5 and a SEQ ID NO: 59 antibody was administered to the same animal model 8 hours before sacrifice, and the brain was harvested. After frozen sectioning, the distribution of fluorescence was observed by confocal microscopy. In
Nanoparticles were prepared by self-assembly by mixing siRNA of SEQ ID NO: 60 or 61, RNA binding peptide of SEQ ID NO: 62, and peptide for penetrating the blood-brain barrier of SEQ ID NO: 40 in a certain ratio. The RNA binding peptide and the peptide for penetrating the blood brain barrier were dissolved in RNase, DNase Free & PCR certified Water (Tech&Innovation, BWA-8000) at a concentration of 5 μg/μL. siRNA was dissolved in RNase, DNase Free & PCR certified Water (Tech&Innovation, BWA-8000) at a concentration of 1 μg/μL. The mixing ratio of siRNA solution and peptide for penetrating the blood-brain barrier was 1:10 to 1:20, and 10 μL of siRNA was mixed with 12 μL (1:10) of peptide solution for penetrating the blood-brain barrier solution in 2 μL increments, and left for at least 30 min. Peptide for penetrating the blood-brain barrier of SEQ ID NO: 63-SEQ ID NO: 40, SEQ ID NO: 64-SEQ ID NO: 40, SEQ ID NO: 65-SEQ ID NO: 40, SEQ ID NO: 66-SEQ ID NO: 40, and SEQ ID NO: 67-SEQ ID NO: 40 also form the complex with siRNA of SEQ ID NO: 60 or SEQ ID NO: 61 in the same manner as above.
The cationic peptide of SEQ ID NO: 9 was dissolved in RNase, DNase Free & PCR certified Water (Tech&Innovation, BWA-8000) at a concentration of 5 μg/μL. The siRNA of SEQ ID NO: 60 or SEQ ID NO: 61 was dissolved in RNase, DNase Free & PCR certified Water (Tech&Innovation, BWA-8000) at a concentration of 1 μg/μL. The mixing ratio of siRNA solution and peptide of SEQ ID NO: 9 was 1:10, and 10 UL of siRNA was mixed with 12 μL (1:10) of peptide solution of SEQ ID NO: 9 in 2 μL increments, and left for at least 30 minutes.
The peptide for penetrating the blood-brain barrier of SEQ ID NO: 70 was dissolved in RNase, DNase Free & PCR certified Water (Tech&Innovation, BWA-8000) at a concentration of 1 μg/μL. The mixture of siRNA and peptide of SEQ ID NO: 9 was mixed with 12 μL of the peptide for penetrating the blood-brain barrier solution of SEQ ID NO: 70 in 2 μL increments and left for at least 30 minutes. The formed complex was confirmed using transmission electron microscopy (TEM, JEOL, JEM 1010) (
The RNA binding peptide of SEQ ID NO: 64 was dissolved in RNase, DNase Free & PCR certified Water (Tech&Innovation, BWA-8000) at a concentration of 5 μg/μL. Beta catenin siRNA (Dhamacon, #J-040628-05) was dissolved in RNase, DNase Free & PCR certified Water (Tech&Innovation, BWA-8000) at a concentration of 1 μg/μL. The mixing ratio of siRNA solution and RNA binding peptide was 1:10, and 10 μL of siRNA was mixed with 12 μL (1:10) of RNA binding peptide solution in 1 μL increments, and left for at least 30 minutes.
The peptide for penetrating the blood-brain barrier of SEQ ID NO: 70 was dissolved in RNase, DNase Free & PCR certified Water (Tech&Innovation, BWA-8000) at a concentration of 1 μg/μL. The mixture of beta catenin siRNA and RNA binding peptide of SEQ ID NO: 64 was mixed with 12 μL of peptide for penetrating the blood-brain barrier solution of SEQ ID NO: 70 in 1 μL increments and left for at least 30 minutes. The formed complex was confirmed using transmission electron microscopy (TEM, JEOL, JEM 1010) (
The peptide of SEQ ID NO: 64 was dissolved in RNase, DNase Free & PCR certified Water (Tech&Innovation, BWA-8000) at a concentration of 5 μg/μL. The siRNA of SEQ ID NO: 60 or SEQ ID NO: 61 was dissolved in RNase, DNase Free & PCR certified Water (Tech&Innovation, BWA-8000) at a concentration of 1 μg/μL. The mixing ratio of siRNA solution and peptide carrier was 1:10, and 10 μL of siRNA was mixed with 12 μL (1:10) of peptide solution of SEQ ID NO: 64 was mixed in 1 μL increments, and left for at least 30 min. The peptide for penetrating the blood-brain barrier of SEQ ID NO: 84 was dissolved in RNase, DNase Free & PCR certified Water (Tech&Innovation, BWA-8000) at a concentration of 1 μg/μL. The mixture of siRNA and peptide of SEQ ID NO: 64 was mixed with 12 μL of the peptide for penetrating the blood-brain barrier solution of SEQ ID NO: 84 in 2 μL increments and left for at least 30 minutes. The formed complex was confirmed using transmission electron microscopy (TEM, JEOL, JEM 1010) (
Using siRNA of SEQ ID NO: 60 or SEQ ID NO: 61 labeled with Alexa Fluor™ 488 (Invitrogen), a complex of peptide for penetrating the blood-brain barrier therewith was prepared in the same manner as in Example 4-1, and the permeability was evaluated using an in vitro BBB model. As a control, Lipofectamine™ 2000 (Invitrogen) was reacted with siRNA of SEQ ID NO: 60 or SEQ ID NO: 61 labeled with Alexa Fluor™ 488 (Invitrogen) according to the manufacturer's method. Immortalized mouse brain endothelial cells (bEnd.3, CRL-2299, ATCC) were seeded at 5×104/well in the upper chamber of culture inserts (corning) and placed in 24 wells. In the lower chamber, 800 μL Dulbecco's modified Eagle's medium (DMEM) was added. The medium was changed every 2 days. Trans-endothelial electrical resistance (TEER) instrument (World Precision Instruments, Inc., Sarasota) was used to monitor the density of the cell layer, and the experiment was performed when the TEER value was 200 Ωcm2 or more. The medium was replaced with DMEM without FBS, and the complex of the peptide for penetrating the blood-brain barrier of SEQ ID NO: 70 labeled with Cy5.5 and siRNA of SEQ ID NO: 60 or SEQ ID NO: 61, and the complex of Lipofectamine™ 2000 and siRNA of SEQ ID NO: 60 or SEQ ID NO: 61 were added to the upper chamber at a concentration of 200 nM each. The assembled transwell was incubated in a shaking incubator at 37° C., 50 rpm for 1, 4 and 8 hours. 500 μL was taken from the lower chamber (basolateral compartment) and the same volume of fresh medium was refilled. The TEER value was rechecked at the end of the experiment. The percentage of transported complex (transport ratio, %) was measured by fluorescence sensitivity using a fluorescence spectrophotometer (Thermo Scientific, USA). In Example 4-2 and Example 4-3, the permeability was also measured in the in vitro BBB model using the same method as above.
This means that the complexes of Example 4 effectively permeabilize the siRNA across the BBB.
The siRNA of SEQ ID NO: 60 or SEQ ID NO: 61 labeled with Alexa Fluor™ 680 (Invitrogen) was used to prepare a complex with peptide for penetrating the blood-brain barrier in the same way as in Example 4-1.
The complex of Example 4-1 and siRNA of SEQ ID NO: 60 or SEQ ID NO: 61 are intravenously administered, respectively, at 150 μg/kg, to hairless mouse (SKH-1, female, 6 weeks old, OrientBio), and the brain was harvested 5 hours later and fluorescence was observed by confocal microscopy (Carl Zeiss LSM700).
Beta catenin siRNA labeled with Alexa Fluor™ 488 (Invitrogen) was used to prepare a complex with peptide for penetrating the blood-brain barrier in the same manner as in Examples 4-2 and 4-3.
The complex of Example 4-2 or 4-3 and beta catenin siRNA at 1 mg/kg are injected intravenously, respectively, at 1 mg/kg, to hairless mouse (SKH-1, female, 6 weeks old, OrientBio), and the brain was harvested 1 hour later and fluorescence was observed by confocal microscopy (Carl Zeiss LSM700).
It was observed whether beta catenin siRNA delivered to brain tissue effectively reduced beta catenin mRNA.
Eight-week-old mouse (C57BL/6, OrientBio) was purchased, and a complex was prepared in the same manner as in Example 4-2 and Example 4-3, and injected intravenously at doses of 2.5 mg/kg and 10 mg/kg (siRNA-based). 24 and 96 hours after injection, blood was removed from the brain tissue by three 20 ml perfusions with PBS. The cerebral cortex, cerebellum and mid brain were isolated, and beta catenin mRNA in the brain tissue was measured by qRT-PCR (Thermo Fisher-QuantStudio 3). PCT conditions and used primer sequences are shown in Table 2 and Table 3, respectively.
The peptide for penetrating the blood-brain barrier of the present invention in which a cell-permeable peptide is linked to the brain endothelial cell surface protein-binding peptide passes through the cell membrane of the brain endothelial cell with excellent efficiency, and the peptide-drug complex in which the peptide for penetrating the blood-brain barrier is combined with a drug such as an antibody, a protein or a therapeutic nucleic acid has the advantage of effectively delivering the drug into the brain parenchyma and maximizing the therapeutic effect of brain diseases and brain tumors.
While the foregoing has described in detail certain aspects of the present invention, it would be apparent to one of ordinary skill in the art that these specific descriptions are merely preferred embodiments and are not intended to limit the scope of the present invention. Accordingly, the substantial scope of the present invention is defined by the appended claims and their equivalents.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10-2021-0130554 | Oct 2021 | KR | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/KR2022/014716 | 9/30/2022 | WO |
