Bioprotac protein having intracellular transmission function and pharmaceutical composition containing the same

Abstract

The present invention relates to a proteolysis targeting chimera (PROTAC) having an intracellular delivery function and a pharmaceutical composition comprising the same. The PROTAC protein according to the present invention has higher solubility than PROTACs prepared by conventional methods, and efficiently degrades endogenous disease proteins when applied to cells, making it effective in treating cancer or inflammatory diseases.

Description

[Technical field]

[0001] The present invention relates to a proteolysis targeting chimera (PROTAC) protein having an intracellular signaling function and a pharmaceutical composition comprising the same. [Background technology]

[0002] Proteolysis targeting chimeras (PROTACs) are dual-binding molecules that bind to disease-causing proteins and induce the proteasome to degrade the proteins, ultimately inducing selective proteolysis. PROTACs consist of two protein-binding molecules, one for binding to E3 ubiquitin ligase and the other for binding to the target protein. By binding to the two proteins, PROTACs bring the target protein into close proximity with the E3 ligase, inducing the tagging, or ubiquitination, of the target protein for subsequent degradation by the proteasome.

[0003] Ubiquitination involves three steps: activation, conjugation, and ligation, which are performed by ubiquitin-activating enzyme (E1), ubiquitin-conjugating enzyme (E2), and ubiquitin ligase (E3). As a result of this sequential cascade, ubiquitin is covalently attached to the target protein. The ubiquitinated protein is finally degraded by the proteasome.

[0004] Protac technology was first launched in 2001 (Sakamoto et al., Proceedings of the National Academy of Sciences of the United States of America. 98: 8554, 2001). Since then, this technology has been used in various drug designs: pVHL, MDM2, β-TrCP1, cereblon, and c-IAP1. Protac drugs have been developed, mostly consisting of low molecular weight compounds. Various types of low molecular weight compounds derived from the thalidomide series have the structural advantage of being able to simultaneously bind target proteins and E3 ligases. Although these known Protac drugs are very useful, they need to be improved to solve the inherent concerns about reduced protein degradation efficiency and safety due to the low solubility and reduced intracellular permeability of low molecular weight compounds, and there is a need for Protac drugs that improve these problems.

[0005] Therefore, instead of using low molecular weight compounds, the present inventors have made intensive efforts to develop a protac protein that has high target protein degradation efficiency and intracellular delivery function. As a result, they have prepared a target protein binding sequence linked to the Von Hippel-Lindau (VHL) protein sequence by a linker consisting of five glycines as a substrate recognition unit that can transfer E3 ligase, which is an important target in cancer, inflammatory diseases, and infections, to a target protein, and have confirmed that an endogenous target protein for a disease is actually degraded through intracellular delivery, thereby completing the present invention.

[0006] The information provided in this Background section is intended solely to enhance understanding of the background of the invention and may not include information that constitutes prior art already known to a person of ordinary skill in the art to which the invention pertains. Summary of the Invention [Problem to be solved by the invention]

[0007] An object of the present invention is to provide a PROTAC protein that has high target protein degradation efficiency and has an intracellular delivery function. Another object of the present invention is to provide a nucleic acid encoding said protac protein. It is still another object of the present invention to provide a pharmaceutical composition comprising the protac protein or a nucleic acid encoding the same as an active ingredient. It is still another object of the present invention to provide a method for preventing or treating a disease, which comprises the step of administering the protac protein or a nucleic acid encoding the same. It is still another object of the present invention to provide a use of said protac protein or a nucleic acid encoding the same for the prevention or treatment of a disease. It is yet another object of the present invention to provide a use of said protac protein or a nucleic acid encoding the same for the manufacture of a medicament for the prevention or treatment of a disease. [Means for solving the problem]

[0008] In order to achieve the above object, the present invention provides a PROTAC protein having the structure of the following Formula 1 or Formula 2: [ka] [ka] In the above Chemical Formula 1 or Chemical Formula 2, (i) PEP is an antibody or a fragment of an antibody, or a cell membrane-penetrating peptide; (ii) L1 and L2 are linkers, L1 and L2 may be the same or different, and L1 is linked to TB or L2; (iii) TB is a binder or conjugate that binds to a target protein; (iv) UR is a binding ligand for ubiquitin ligase; (v) n and m each independently represent an integer of 1 to 10. The present invention also provides a nucleic acid encoding said protac protein. The present invention also provides a pharmaceutical composition comprising the protac protein or a nucleic acid encoding the same as an active ingredient. The present invention also provides a method for preventing or treating a disease, comprising the step of administering the protac protein or a nucleic acid encoding the same. The present invention also provides the use of said protac protein or a nucleic acid encoding the same for the prevention or treatment of a disease. The present invention also provides use of the protac protein or a nucleic acid encoding the same for the manufacture of a medicament for the prevention or treatment of a disease. [Brief description of the drawings]

[0009] [Figure 1] FIG. 1 is a schematic diagram of an expression vector for a Protac protein having cell-penetrating ability. [Diagram 2] This shows the results of Western blot analysis of the protac protein expressed by the plasmid introduced into cells. [Diagram 3] This shows the results of cancer cell survival rate depending on the PROTAC protein expressed by a plasmid introduced into the cells. [Figure 4] This is a Western blot result confirming the suppression of active KRAS expression by the protak protein expressed by the plasmid introduced into the cells. [Diagram 5] This is a Western blot result confirming the expression of protak protein and the suppression of active KRAS expression in cells after introducing mRNA encoding protak protein into cells. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0010] Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one skilled in the art to which this invention belongs. Generally, the nomenclature used herein and the laboratory procedures described below are those well known and commonly employed in the art.

[0011] The present invention is based on the discovery that a ubiquitin pathway protein will ubiquitinate any target protein when the ubiquitin pathway protein and the target protein are in close proximity to a chimeric structure that binds the ubiquitin pathway protein and the target protein.

[0012] The main reason for the present invention is to overcome the limitations of PROTAC technology produced by conventional methods, such as low actual solubility or inability to effectively degrade endogenous disease proteins when applied to cells. In one aspect, the present invention relates to a PROTAC protein having the structure of Formula 1 or Formula 2 below: [ka] [ka] In the above Chemical Formula 1 or Chemical Formula 2, (i) PEP is an antibody or a fragment of an antibody, or a cell penetrating peptide; (ii) L1 and L2 are linkers, L1 and L2 may be the same or different, and L1 is linked to TB or L2; (iii) TB is a binder or conjugate that binds to a target protein; (iv) UR is a binding ligand for ubiquitin ligase; (v) n and m each independently represent an integer of 1 to 10.

[0013] As used herein, the term "PROTAC" is an abbreviation for proteolysis targeting chimera, and refers to a bifunctional small molecule composed of two active domains and a linker, which can remove specific unwanted proteins. As used herein, "PROTAC protein" is used interchangeably with "bioPROTAC protein" and "chimeric protein."

[0014] The Protac proteins according to the present invention are capable of inducing ubiquitination of a selected target protein and are designed to link a target protein binding moiety and a linker to contain a ubiquitin ligase binding site.

[0015] In the present invention, the Protac protein comprises a ligand that binds to ubiquitin ligase at one end and a portion that binds to a target protein at the other end, and comprises a cell-permeable domain at the end of the protein that binds to the target protein or at the linker that connects the ubiquitin ligase-binding ligand to the target protein-binding portion, which allows the Protac protein to be located in close proximity to the target protein when introduced into cells and induce protein degradation, and is present at a high concentration in cells depending on the numbers n and m, thereby inducing effective degradation of the target protein. In the present invention, the protac protein can be characterized by being represented by the amino acid sequences of SEQ ID NOs: 1 to 6, but is not limited thereto.

[0016] SEQ ID NO:1: EVQLLESGGGLVQPGGSLRLSCAASGTFSTFSMNWVRQAPGKGLEWVSYISRTSKTIYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARGRFFDYWGQGTLVTVSSGGSEGK SSGSGSESKSTGGSDIQMTQSPSSLSASVGDRVTITCRASQSISSYLNWYQQKKPGEAPKLLIYSASVLQSGVPSRFSGSGSGTDFTLTISSLQPEDFATYYCQQSVMIPMTFGQGTKVEIK GSGGGGSMPRRAENWDEAEVGAEEAGVEEYGPEEDGGEESGAEESGPEESGPEELGAEEEMEAGRPRPVLRSVNSREPSQVIFCNRSPRVVLPVWLNFDGEPQPYPTLPPGTGRRIHSYRG HLWLFRDAGHTHDGLLVNQTELFVPSLNVDGQPIFANITLPVYTLKERCLQVVRSLVKPENYRRLDIVRSLYEDLEDHPNVQKDLERLTQERIAHQRMGDENLYFQGGSGGSGGSHHHHHHHHH

[0017] SEQ ID NO:2: MAWVWTLLFLLMAAAQSIQAVSRRRRRRGGRRRRGGGGSEVQLLESGGGLVQPGGSLRLSCAASGTFSTFSMNWVRQAPGKGLEWVSYISRTSKTIYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTA VYYCARGRFFDYWGQGTLVTVSSGGSEGKSSGSGSESKSTGGSDIQMTQSPSSLSASVGDRVTITCRASQSISSYLNWYQQKPGEAPKLLIYSASVLQSGVPSRFSGSGSGTDFTLTISSLQPEDFATYYC QQSVMIPMTFGQGTKVEIKGSGGGGSMPRRAENWDEAEVGAEEAGVEEYGPEEDGGEESGAEESGPEESGPEELGAEEEMEAGRPRPVLRSVNSREPSQVIFCNRSPRVVLPVWLNFDGEPQPYPTLPGT GRRIHSYRGHLWLFRDAGTHDGLLVNQTELFVPSLNVDGQPIFANITLPVYTLKERCLQVVRSLVKPENYRRLDIVRSLYEDLEDHPNVQKDLERLTQERIAHQRMGDENLYFQGGSGGSGGSHHHHHHHH

[0018] SEQ ID NO:3: MAWVWTLLFLMAAAQSIQAEVQLLESGGGLVQPGGSLRLSCAASGFTFSTFSMNWVRQAPGKGLEWVSYISRTSKTIYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARGRFFDYWGQGTLV TVSSGGSEGKSSGSGSESKSTGGSDIQMTQSPSSLSASVGDRVTITCRASQSISSYLNWYQQKKPGEAPKLLIYSASVLQSGVPSRFSGSGSGTDFTLTISSLQPEDFATYYCQQSVMIPMTFGQGTKVEIK GSGGGGSMPRRAENWDEAEVGAEEAGVEEYGPEEDGGEESGAEESGPEESGPEELGAEEEMEAGRPRPVLRSVNSREPSQVIFCNRSPRVVLPVWLNFDGEPQPYPTLPPGTGRIHSYRGHLWLFRDAGT HDGLLVNQTELFVPSLNVDGQPIFANITLPVYTLKERCLQVVRSLVKPENYRRLDIVRSLYEDLEDHPNVQKDLERLTQERIAHQRMGDGGGSVSRRRRRRGGRRRRENLYFQGGSGGSGGSHHHHHHHH

[0019] SEQ ID NO:4: EVQLLESGGGLVQPGGSLRLSCAASGTFSTFSMNWVRQAPGKGLEWVSYISRTSKTIYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARGRFFDYWGQGTLVTVSSG GSEGKSSGSGSESKSTGGSDIQMTQSPSSLSASVGDRVTITCRASQSISSYLNWYQQKKPGEAPKLLIYSASVLQSGVPSRFSGSGSGTDFTLTISSLQPEDFATYYCQQSVMIPMT FGQGTKVEIKGSGGGGSMENRWQVMIVWQVDRMRIRTWKSLVKHHMYVSGKARGWFYRHHYESPHPRISSEVHIPLGDARLVITTYWGLHTGERDWHLGQGVSIEWRKKRYSTQVD PELADQLIHLYYFDCFSDSAIRKALLGHIVSPRCEYQAGHNKVGSLQYLALAALITPKKIKPPLPSVTKLTEDRWNKPQKTKGHRGSHTMNGHENLYFQGGSGGSGGSHHHHHHHH

[0020] SEQ ID NO:5: MAWVWTLLFLLMAAAQSIQAVSRRRRRRGGRRRRGGGGSEVQLLESGGGLVQPGGSLRLSCAASGTFSTFSMNWVRQAPGKGLEWVSYISRTSKTIYYADSVKGRFTISRDNSKNTLYLQMNSLR AEDTAVYYCARGRFFDYWGQGTLVTVSSGGSEGKSSGSGSESKSTGGSDIQMTQSPSSLSASVGDRVTITCRASQSISSYLNWYQQKKPGEAPKLLIYSASVLQSGVPSRFSGSGSGTDFTLTISSL QPEDFATYYCQQSVMIPMTFGQGTKVEIKGSGGGGSMENRWQVMIVWQVDRMRIRTWKSLVKHHMYVSGKARGWFYRHHYESPHPRISSEVHIPLGDARLVITTYWGLHTGERDWHLGQGVSIEW RKKRYSTQVDPELADQLIHLYYFDCFSDSAIRKALLGHIVSPRCEYQAGHNKVGSLQYLALAALITPKKIKPPLPSVTKLTEDRWNKPQKTKGHRGSHTMNGHENLYFQGGSGGSGGSHHHHHHHH

[0021] SEQ ID NO:6: MAWVWTLLFLMAAAQSIQAEVQLLESGGGLVQPGGSLRLSCAASGFTFSTFSMNWVRQAPGKGLEWVSYISRTSKTIYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARGRFFDYWG QGTLVTVSSGGSEGKSSGSGSESKSTGGSDIQMTQSPSSLSASVGDRVTITCRASQSISSYLNWYQQKPGEAPKLLIYSASVLQSGVPSRFSGSGSGTDFTLTISSLQPEDFATYYCQQSVMIPMT FGQGTKVEIKGSGGGGSMENRWQVMIVWQVDRMRIRTWKSLVKHHMYVSGKARGWFYRHHYESPHPRISSEVHIPLGDARLVITTYWGLHTGERDWHLGQGVSIEWRKKRYSTQVDPELADQLIH LYYFDCFSDSAIRKALLGHIVSPRCEYQAGHNKVGSLQYLALAALITPKKIKPPLPSVTKLTEDRWNKPQKTKGHRGSHTMNGHGGGGSVSRRRRRRGGRRRRENLYFQGGSGGSGGSHHHHHHHH

[0022] A binder or conjugate that binds to a target protein, designated as TB in the present invention, can be selected from a library. The TB is designed to couple to a ubiquitin pathway protein binding moiety, such as a VHL protein, through a linker. The ubiquitin pathway protein recognizes an E3 ubiquitin ligase.

[0023] In the present invention, the target proteins of the Protac protein include, but are not limited to, mutated RAS superfamily, kinases, transcription factors, and phosphatases. In the present invention, the RAS superfamily may be characterized as being selected from the group consisting of KRAS, HRAS, and NRAS.

[0024] In the present invention, the TB is selected from the group consisting of mutated RAS superfamily inhibitors, kinase inhibitors, phosphatase inhibitors, heat shock protein 90 (HSP90) inhibitors, mouse double minute 2 homolog (MDM2) inhibitors, histone deacetylases (HDAC) inhibitors, human lysine methyltransferase inhibitors, angiogenesis inhibitors, immunosuppressive compounds, compounds targeting human BET (bromodomain and extraterminal domain) bromodomain-containing proteins, compounds targeting aryl hydrocarbon receptor (AHR), compounds targeting epithelial growth factor (EGF) receptor kinase, compounds targeting FKBP (FK506 binding protein), compounds targeting androgen receptor (AR), compounds targeting estrogen receptor (ER), compounds targeting thyroid hormone receptor, compounds targeting HIV protease, compounds targeting HIV integrase, compounds targeting HCV protease, acyl-protein thioesterase 1; The compound may be characterized as being selected from the group consisting of compounds targeting acyl-protein thioesterase-2 (APT2), but is not limited thereto.

[0025] In the present invention, the TB can be characterized as being a peptide containing any one of the amino acids in SEQ ID NO: 7 to SEQ ID NO: 14, but is not limited thereto.

[0026] SEQ ID NO: 7: LTPHKHHKHLHA SEQ ID NO: 8: WPGKHHNHYLRS SEQ ID NO: 9: HDGYWWHSMTMW SEQ ID NO:10: LIHPMTVKHVHL SEQ ID NO: 11: GSHWHFPKHQQQ SEQ ID NO: 12: GSHWHFPKHQQH SEQ ID NO: 13: WPGKHHHHYLRR SEQ ID NO:14: EVQLLESGGGLVQPGGSLRLSCAASGTFSTFSMNWVRQAPGKGLEWVSYISRTSKTIYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARGRFFDYWGQGTLVTVSSGGSEGK SSGSGSESKSTGGSDIQMTQSPSSLSASVGDRVTITCRASQSISSYLNWYQQKKPGEAPKLLIYSASVLQSGVPSRFSGSGSGTDFTLTISSLQPEDFATYYCQQSVMIPMTFGQGTKVEIK

[0027] In the present invention, the UR may be characterized as a ligand that binds to an E3 ligase selected from the group consisting of XIAP (X-linked inhibitor of apoptosis protein), VHL (Von Hippel-Lindau) protein, IAPs (inhibitor of apoptosis proteins), cereblon, and MDM2 (Mouse double minute 2 homolog), as a binding ligand for ubiquitin ligase, but is not limited thereto.

[0028] In the present invention, the PEP may be characterized as being an antibody or an antibody fragment, or a cell penetrating peptide.

[0029] In the present invention, the cell membrane-permeable peptide is a peptide having specific permeability to target disease cells. Examples of usable cell membrane-permeable peptide sequences are shown in Table 1 below, but are not limited thereto. [Table 1]

[0030] In the present invention, the antibody is selected from the group consisting of EGFR, DLL3, EDAR, CLL1, BMPR1B, E16, STEAP1, 0772P, MPF, NaPi2b, Sema 5b, and PSCA. The polypeptides may be characterized as binding to one or more of the polypeptides selected from the group consisting of, but not limited to, hlg, ETBR, MSG783, STEAP2, TrpM4, CRIPTO, CD21, CD79b, FcRH2, B7-H4, HER2, NCA, MDP, IL20Rct, brevican, EphB2R, ASLG659, PSCA, GEDA, BAFF-R, CD22, CD79a, CXCRS, HLA-DOB, P2X5, CD72, LY64, FcRH1, IRTA2, TENB2, PMEL17, TMEFF1, GDNF-Ra1, Ly6E, TMEM46, Ly6G6D, LGR5, RET, LY6K, GPR19, GPR54, ASPHD1, tyrosinase, TMEM118, GPR172A, MUC16, and CD33.

[0031] In the present invention, the antibody may be characterized as being a monoclonal antibody or a variant thereof, and the monoclonal antibody may be selected from the group consisting of trastuzumab, cetuximab, rituximab, brentuximab, gemtuzumab, inotuzumab, sacituzumab, alemtuzumab, and nimotuzumab, but is not limited thereto. From another aspect, the present invention relates to a nucleic acid encoding the protac protein.

[0032] In the present invention, the nucleic acid may be DNA, mRNA, plasmid DNA, etc., and the gene encoding the protease protein, for example, plasmid DNA and the mRNA derived therefrom, can be delivered into cells by cell-permeable functional nanocarriers to exert the same targeted protein degradation effect.

[0033] In the present invention, the nucleic acid can be used together with various carriers such as lipid nanoparticles (LNPs) and liposomes, which are conventionally known to effectively deliver oligonucleotides into cells, but are not limited thereto. From another aspect, the present invention relates to a pharmaceutical composition comprising the protac protein or a nucleic acid encoding the protac protein. The present invention provides a wide range of pharmaceutical compositions that are consistent with the degradation of target proteins and that relate to the Protak proteins according to the present invention.

[0034] In the present invention, the pharmaceutical composition may be for the treatment or prevention of cancer or an inflammatory disease, and may be for the treatment or prevention of a disease selected from the group consisting of cancer, asthma, autoimmune disease, rheumatoid arthritis, multiple sclerosis, cilia disease, cleft palate, diabetes, heart disease, hypertension, inflammatory bowel disease, mental retardation, mood disorder, obesity, refractive error, infertility, Angelman syndrome, Canavan disease, chronic digestive disorder, Charcot-Marie-Tooth disease, cystic fibrosis, Duchenne muscular dystrophy, hemochromatosis, hemophilia, Klinefelter syndrome, neurofibromatosis, phenylketonuria, autosomal dominant polycystic idiopathies (PKD1 or PKD2), Prader-Willi syndrome, sickle cell anemia, Tay-Sachs disease, Turner syndrome, HIV infection, and HCV infection.

[0035] In the present invention, the cancer includes squamous cell carcinoma, basal cell carcinoma, adenocarcinoma, hepatocellular carcinoma, renal cell carcinoma, bladder cancer, intestinal cancer, breast cancer, cervical cancer, uterine cancer, colon cancer, esophageal cancer, head cancer, kidney cancer, liver cancer, lung cancer, ovarian cancer, pancreatic cancer, prostate cancer, gastric cancer, leukemia, benign and malignant lymphoma, particularly Bukit's lymphoma and non-Hodgkin's lymphoma, benign and malignant melanoma, myeloproliferative disorders, Ewing's sarcoma, blood vessels, The tumor may be characterized as being selected from the group consisting of sarcoma, Kaposi's sarcoma, liposarcoma, myosarcoma, neuroepithelial sarcoma, synovial sarcoma, neurosarcoma, astrocytoma, oligodendroglioma, ependymoma, glioblastoma, neuroblastoma, ganglioneuroma, ganglioglioma, medulloblastoma, pinealocytoma, meningioma, meningeal sarcoma, neurofibromatosis, and schwannoma, testicular cancer, thyroid cancer, carcinosarcoma, Hoggins' disease, Wilms' tumor, and teratocarcinoma.

[0036] In the present invention, the inflammatory disease may be characterized as being selected from the group consisting of arthritis, autoimmune diseases, Parkinson's disease, dementia, hepatitis, and viral infections.

[0037] The pharmaceutical compositions of the present invention may be administered orally, parenterally, by inhalation spray, topically, rectally, nasally or via an implanted reservoir, and when administered orally or parenterally, nanoparticles or liposomes may be administered as a carrier.

[0038] In one embodiment of the present invention, the single dose of the protac protein is 1 ng / kg to 100 mg / kg, preferably 5 ng / kg to 50 mg / kg, and can be characterized as being administered once a day or 1 to 3 times a week, although the dose and administration interval are not limited to these.

[0039] From another aspect, the present invention relates to a method for preventing or treating a disease, which comprises the step of administering the protac protein or a nucleic acid encoding the protac protein. From another aspect, the present invention relates to use of the protac protein or a nucleic acid encoding the protac protein for the prevention or treatment of a disease.

[0040] From another aspect, the present invention relates to use of the protac protein or a nucleic acid encoding the protac protein for the manufacture of a medicament for the prevention or treatment of a disease. In the present invention, the disease may be characterized as being, but is not limited to, cancer or an inflammatory disease.

[0041] In the present invention, the methods, uses and applications include the protac protein of the present invention or a nucleic acid encoding the same, and relate to a pharmaceutical composition comprising the protac protein or a nucleic acid encoding the same, and the description of the contents overlapping with the above-mentioned protac protein or the nucleic acid encoding the same and pharmaceutical composition will be omitted.

[0042] The present invention will be described in more detail with reference to the following examples. It will be obvious to those skilled in the art that these examples are merely for the purpose of illustrating the present invention and are not intended to limit the scope of the present invention. EXAMPLES

[0043] Example 1: Expression of cell-permeable protac protein in mammalian cells The present inventors designed an expression vector for a protak protein that degrades a target protein as follows. G12CA cDNA containing a monoclonal antibody targeting VHL protein that binds to E3 ligase and a Kozak sequence that binds to ribosomes and helps transcription was inserted into the pcDNA3.4 vector, cloned, and confirmed by DNA sequencing. The signal peptide, linker, and PEP sequence were added to the constructed plasmid DNA sequence. The signal peptide was located at the N-terminus, followed by a monoclonal antibody targeting mutant human KRAS G12C, VHL, and PEP linked to this by linkers of various lengths in various orders. The plasmid constructed in this way (Figure 1) was transfected into CHO-S cell line, and then enhancer was added and cultured for 7 days.

[0044] The expressed Protac protein was measured by Western blotting using anti-His tag antibody (Abcam, ab18184) and anti-VHL antibody (Invitrogen, MA5-13940), and the Western blotting results are shown in Figure 2. The theoretical protein size is 56 kDa, and Protac protein began to appear from day 3 of culture. Since the His Tag did not appear from day 5 of culture onwards, it is considered to have been cleaved from the protein.

[0045] Example 2: Confirmation of the effect of Protac protein in suppressing cancer cell proliferation A plasmid encoding Protak was transfected into cancer cells, and an MTT assay was performed to examine the anticancer effect of the Protak protein expressed by the plasmid. G12C 5X10 cells of non-small cell lung cancer with the phenotype 3Various amounts of plasmids were transfected into H358 (ATCC, CRL-5807) using Lipofectamine 3000 (Invitrogen, L3000001), and cell viability was evaluated by MTT assay 72 hours later (Figure 3). The higher the concentration of the treated plasmid, the lower the viability of H358 cells. This confirms that the protac protein was expressed and acted on the cells by the plasmid introduced into them.

[0046] Example 3: Confirmation of the effect of Protak protein in suppressing KRAS signal transduction To confirm that the target protein is degraded by the protactic protein expressed in the cells, the plasmid DNA prepared in Example 1 was transfected with human KRAS using Lipofectamine 3000 (Invitrogen, L3000001). G12C The cells were transfected into H358 (ATCC, CRL-5807), a non-small cell lung cancer cell line with the phenotype of . After transfection, the cells were lysed every 16, 24, and 48 hours to obtain cell lysates.

[0047] To isolate active KRAS, 80μg of GST-Raf1-RBD was added using the Active GTPase Kit (Cell signaling, 11860S) and 500μg of protein was dispensed into a spin cup. After 1 hour of reaction at 4℃ and 15 seconds of centrifugation at 6000xg, the column was transferred to a new tube and 400μL of 1x lysis buffer was added. After 15 seconds of centrifugation at 6000xg, the column was transferred to a new tube and 50μL of 2x SDS buffer (5X SDS Sample loading dye 200μl, Water 300μl mixture) was dispensed and reacted for 2 minutes. After 2 minutes of centrifugation at 6000xg, the column was heated at 100℃ for 7 minutes. Proteins (protein loading volume 20μl / lane) were separated by electrophoresis on 11% SDS-PAGE and transferred to a nitrocellulose membrane. To measure ERK1 / 2, a sub-signal of KRAS, 30μg of protein was electrophoresed on 11% SDS-PAGE and transferred to nitrocellulose membrane. After blocking with 5% skim milk dissolved in T-TBS for 1 hour, primary antibody was diluted 1:1000 in T-TBS and reacted overnight at 4℃ with inverting. After washing with T-TBS three times for 10 minutes each, secondary antibody was diluted 1:3000 in T-TBS and reacted at room temperature for 1 hour with inverting. After washing with T-TBS three times for 10 minutes each, chemiluminescence was performed with ECL substrate (Thermo, 34580) and confirmed with Amersham Imager 680 (GE). Information on the antibodies used is shown in Table 2 below.

[0048] [Table 2]

[0049] The protak protein was identified using an anti-His tag antibody by immunoblotting to confirm the expression of all KRAS (pan KRAS) or activated KRAS (active KRAS) in the cells (Figure 4). As the protak protein was expressed, the expression level of activated KRAS decreased, but the expression level of pan KRAS did not change. This confirms that the protak protein selectively degrades only activated KRAS and not normal pan KRAS. Example 4: Intracellular introduction of mRNA encoding a protac protein

[0050] To express the protak protein in cells, it was prepared in the form of mRNA instead of a plasmid. 5' capping and 3' poly A tail were inserted to increase the stability of the mRNA. The cells were transfected using Lipofectamine MessngerMAX (Invitrogen, LMRNA003). 24 hours after transfection, the cells were lysed to obtain cell lysates. Activated KRAS was selected in the same manner as described in Example 3. The protak protein expressed by the mRNA introduced into the cells was confirmed using an anti-His tag antibody (Abcam) by immunoblotting. It was confirmed that the expression level of activated KRAS decreased as the protak protein was expressed (Figure 5). The protak protein introduced in the form of mRNA was expressed, and the target protein, activated KRAS, was degraded. [Industrial Applicability]

[0051] The PROTAC protein according to the present invention has higher solubility than PROTACs produced by conventional methods, and efficiently degrades endogenous disease proteins when applied to cells, making it effective in treating cancer or inflammatory diseases.

[0052] Although the specific parts of the present invention have been described in detail above, it is clear to those skilled in the art that such specific techniques are merely preferred embodiments and do not limit the scope of the present invention. Therefore, the substantial scope of the present invention is defined by the appended claims and their equivalents.

Claims

1. A nucleic acid sequence comprising an amino acid sequence selected from SEQ ID NO: 1 to SEQ ID NO: 6, A PROTAC protein comprising a binder or conjugate that binds to a target protein; a linker; a ligand that binds to a ubiquitin ligase; and a cell penetrating peptide.

2. The protac protein of claim 1 , wherein the target protein is a mutated KRAS superfamily protein.

3. The protac protein according to claim 1, characterized in that the binder or binder that binds to the target protein is a peptide comprising the amino acid sequence of SEQ ID NO:

14.

4. The protac protein according to claim 1, characterized in that the binding ligand to the ubiquitin ligase is a VHL protein that binds to an E3 ligase.

5. A nucleic acid encoding the protac protein of claim 1.

6. A pharmaceutical composition comprising the protac protein according to any one of claims 1 to 4 or the nucleic acid according to claim 5.

7. The pharmaceutical composition according to claim 6, which is for treating or preventing cancer or an inflammatory disease.

8. 8. The pharmaceutical composition of claim 7, wherein the cancer is selected from the group consisting of squamous cell carcinoma, basal cell carcinoma, adenocarcinoma, hepatocellular carcinoma, renal cell carcinoma, bladder cancer, intestinal cancer, breast cancer, cervical cancer, uterine cancer, colon cancer, esophageal cancer, head cancer, kidney cancer, liver cancer, lung cancer, ovarian cancer, pancreatic cancer, prostate cancer, gastric cancer, leukemia, benign and malignant lymphoma, benign and malignant melanoma, myeloproliferative disorders, Ewing's sarcoma, angiosarcoma, Kaposi's sarcoma, liposarcoma, myosarcoma, neuroepithelial sarcoma, synovial sarcoma, neurosarcoma, astrocytoma, oligodendroglioma, ependymoma, glioblastoma, neuroblastoma, ganglioneuroma, ganglioglioma, medulloblastoma, pineal cell tumor, meningioma, meningeal sarcoma, sarcoma including neurofibromatosis and schwannoma, testicular cancer, thyroid cancer, carcinosarcoma, Hoggins' disease, Wilms' tumor, and teratocarcinoma.

9. The pharmaceutical composition according to claim 7, wherein the inflammatory disease is selected from the group consisting of arthritis, autoimmune diseases, Parkinson's disease, dementia, hepatitis and viral infections.

10. 8. The pharmaceutical composition according to claim 7, which is administered orally, parenterally, by inhalation spray, topically, rectally, nasally or via an implanted reservoir.

11. The pharmaceutical composition according to claim 10, wherein the pharmaceutical composition is administered orally or parenterally using nanoparticles or liposomes as a carrier.

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