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Kafe 바로가기국가/구분 | United States(US) Patent 등록 |
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국제특허분류(IPC7판) |
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출원번호 | US-0878400 (2015-10-08) |
등록번호 | US-9814760 (2017-11-14) |
발명자 / 주소 |
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출원인 / 주소 |
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대리인 / 주소 |
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인용정보 | 피인용 횟수 : 0 인용 특허 : 395 |
The invention relates to compositions and methods for the preparation, manufacture and therapeutic use of polynucleotides, primary transcripts and mmRNA molecules.
1. An isolated mRNA comprising; (a) a first region comprising an open reading frame having at least 95% identity to SEQ ID NO: 1871 encoding a polypeptide having the sequence of SEQ ID NO: 967 consisting of nucleotides selected from 1-methyl-pseudouridine, cytidine, adenosine, and guanosine;(b) a fi
1. An isolated mRNA comprising; (a) a first region comprising an open reading frame having at least 95% identity to SEQ ID NO: 1871 encoding a polypeptide having the sequence of SEQ ID NO: 967 consisting of nucleotides selected from 1-methyl-pseudouridine, cytidine, adenosine, and guanosine;(b) a first flanking region located at the 5′ terminus of said first region comprising; (i) a 5′-UTR including a Kozak sequence; and(ii) at least one 5′ terminal cap;(c) a second flanking region located at the 3′ terminus of said first region comprising; (i′) a 3′-UTR; and(ii′) a 3′ tailing sequence of linked nucleosides. 2. The isolated mRNA of claim 1 wherein the open reading frame comprises the sequence of SEQ ID NO: 1871. 3. The isolated mRNA of claim 1, wherein the 3′ tailing sequence of linked nucleosides is selected from the group consisting of a poly-A tail of approximately 160 nucleotides and a polyA-G quartet. 4. The isolated mRNA of claim 1 which is purified. 5. The isolated mRNA of claim 1, wherein the at least one 5′ terminal cap is selected from the group consisting of Cap0, Cap1, ARCA, inosine, N1-methyl-guanosine, 2′fluoro-guanosine, 7-deaza-guanosine, 8-oxo-guanosine, 2-amino-guanosine, LNA-guanosine, and 2-azido-guanosine. 6. The isolated mRNA of claim 1, further comprising a targeting moiety, wherein said targeting moiety is covalently bound to said polynucleotide. 7. The isolated mRNA of claim 6, wherein said targeting moiety is an antibody, thyrotropin, melanotropin, lectin, glycoprotein, surfactant protein A, Mucin carbohydrate, multivalent lactose, multivalent galactose, N-acetyl-galactosamine, N-acetyl-gulucosamine multivalent mannose, multivalent fucose, glycosylated polyaminoacids, multivalent galactose, transferrin, bisphosphonate, polyglutamate, polyaspartate, a lipid, cholesterol, a steroid, bile acid, folate, vitamin B12, biotin, an RGD peptide, an RGD peptide mimetic, or an aptamer. 8. A pharmaceutical composition comprising the isolated mRNA of claim 1. 9. A pharmaceutical composition comprising a plurality of lipid nanoparticles, wherein the plurality of lipid nanoparticles has a mean particle size of between 80 nm and 160 nm, a mean PDI of between 0.02 and 0.2, and a mean lipid to polynucleotide ratio (wt/wt) of between 10 and 20; and wherein the lipid nanoparticles comprise the isolated mRNA of claim 1 and a pharmaceutically acceptable excipient. 10. The pharmaceutical composition of claim 9, wherein the excipient is selected from a solvent, aqueous solvent, non-aqueous solvent, dispersion media, diluent, dispersion, suspension aid, surface active agent, isotonic agent, thickening or emulsifying agent, preservative, lipid, lipidoids liposome, lipid nanoparticle, core-shell nanoparticles, polymer, lipoplex, peptide, protein, cell, hyaluronidase, and mixtures thereof. 11. The pharmaceutical composition of claim 10, where the pharmaceutical composition comprises a lipid and wherein said lipid is selected from DLin-DMA, DLin-K-DMA, DLin-KC2-DMA, 98N12-5, C12-200, DLin-MC3-DMA, DODMA, DSDMA, DLenDMA, reLNPs, PLGA and PEGylated lipids and mixtures thereof. 12. A method of producing a polypeptide of interest in a mammalian cell, tissue or organism comprising administering to said cell, tissue or organism the the pharmaceutical composition of claim 9.
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