US2011287015A1PendingUtilityA1
Mg53 compositions and methods of use
Est. expiryJul 11, 2026(expired)· nominal 20-yr term from priority
A61P 9/10A61P 9/02A61P 37/06A61P 9/12A61P 9/04A61P 9/00A61P 39/06A61P 7/02A61P 37/08A61P 3/10A61P 37/02A61P 37/04A61P 41/00A61P 43/00A61P 7/04A61P 3/14A61P 31/18A61P 25/18A61P 25/28A61P 29/00A61P 25/00A61P 25/22A61P 35/00A61P 25/04A61P 31/12A61P 25/14A61P 25/16A61P 3/04A61P 33/00A61P 25/24A61P 25/08A61P 31/04A61P 11/06A61P 1/04C07K 16/18A61P 13/08A61P 13/02A61P 11/02A01K 2217/075C07K 2319/10A61P 21/00C07K 14/4702A61P 17/02C40B 30/06A61P 21/04A61P 17/00C12N 15/8509A01K 67/0276A61P 19/10A61P 1/14A61P 17/10A61P 15/00A61P 15/08A61P 17/16A61P 1/02C40B 40/02A01K 2267/0375A01K 2227/105A61P 17/06A61P 17/14A61P 13/12
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Abstract
Disclosed herein are nucleic acid sequences that encode novel polypeptides. Also disclosed are polypeptides encoded by these nucleic acid sequences, and antibodies, which immunospecifically-bind to the polypeptide, as well as derivatives, variants, mutants, or fragments of the aforementioned polypeptide, polynucleotide, or antibody. The invention further discloses therapeutic, diagnostic and research methods for diagnosis, treatment, and prevention of disorders involving any one of these novel human nucleic acids and proteins.
Claims
exact text as granted — not AI-modified1 . An isolated anti-MG53 antibody comprising at least two complementarity determining regions (CDRs), wherein the antibody specifically binds to at least one amino acid residue selected from residues 1-477 of the amino acid sequence of at least one of SEQ ID NO: 1, 3, 5 or 7.
2 . The antibody of claim 1 , wherein the antibody specifically binds to at least one amino acid residue selected from residues 1-144 of the amino acid sequence of at least one of SEQ ID NO: 1, 3, 5 or 7.
3 . The antibody of claim 1 , wherein the antibody specifically binds to at least one amino acid residue selected from residues 2-62 of the amino acid sequence of at least one of SEQ ID NO: 1, 3, 5 or 7.
4 . The antibody of claim 1 , wherein the antibody specifically binds to at least one amino acid residue selected from residues 2-268 of the amino acid sequence of at least one of SEQ ID NO: 1, 3, 5 or 7.
5 . The antibody of claim 1 , wherein the antibody specifically binds to at least one amino acid residue selected from residues 246-477 of the amino acid sequence of at least one of SEQ ID NO: 1, 3, 5 or 7.
6 . The antibody of claim 1 , wherein the anti-MG53 antibody is a member selected from the group consisting of a polyclonal antibody, a monoclonal antibody, and a bispecific antibody.
7 . The antibody of claim 6 , wherein the antibody is monoclonal.
8 . The antibody of claim 7 , wherein the monoclonal antibody is at least one of chimeric, humanized, or a fully human antibody.
9 . The antibody of claim 8 , wherein the antibody is at least one of a single chain, a single domain, or a antibody fragment.
10 . The antibody of claim 9 , wherein the fragment is selected from the group consisting of an Fv fragment, an Fab fragment, an Fab′ fragment, and an F(ab′) 2 fragment.
11 . The antibody of claim 6 , wherein the bispecific antibody comprises at least one variable region capable of specifically binding MG53.
12 . The antibody of claim 9 , wherein the single chain, single domain or antibody fragment comprises at least one heavy (H) chain variable region (VH) CDR.
13 . The antibody of claim 9 , wherein the single chain, single domain or antibody fragment comprises at least one light (L) chain variable region (VL) CDR.
14 . The antibody of claim 13 , wherein the light chain is a kappa chain or a lambda chain.
15 . The antibody of claim 1 , wherein the antibody is a type selected from the group consisting of IgG, IgM, IgA, IgE and IgD.
16 . A composition comprising an effective amount of the antibody of claim 1 and a pharmaceutically acceptable carrier or excipient.
17 . A method of treating or diagnosing an MG53-related condition comprising contacting or administering the composition of claim 16 to a cell, tissue, organ or individual, wherein the composition is effective for treating or diagnosing the MG53-related condition.
18 . The method of claim 17 wherein an amount of antibody administered to an the individual is from about 0.1 mg/kg to about 2000 mg/kg.
19 . The method of claim 17 , wherein the antibody is administered by at least one route selected from intravenously, intraperitoneally, intramuscularly, and subcutaneously.
20 . An isolated and/or recombinant anti-MG53 antibody wherein the antibody specifically binds to an epitope within a polypeptide having at least 90% sequence identity to the amino acid sequence of SEQ ID NO: 1.
21 . The antibody of claim 20 , wherein the antibody specifically binds to an epitope within residues 1-144 of the amino acid sequence of SEQ ID NO: 1.
22 . An isolated nucleic acid encoding the antibody of claim 1 or a portion thereof.
23 . A host cell comprising the nucleic acid of claim 22 .
24 . The antibody of claim 1 , wherein the antibody comprises at least one heavy chain or light chain CDR.Cited by (0)
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