Innovative discovery of therapeutic, diagnostic, and antibody compositions related to protein fragments of Valyl-tRNA synthetases
US-9556425-B2 · Jan 31, 2017 · US
US10189911B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10189911-B2 |
| Application number | US-201615365104-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 30, 2016 |
| Priority date | Apr 29, 2010 |
| Publication date | Jan 29, 2019 |
| Grant date | Jan 29, 2019 |
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Provided are compositions comprising newly identified protein fragments of aminoacyl-tRNA synthetases, polynucleotides that encode them and complements thereof, related agents, and methods of use thereof in diagnostic, drug discovery, research, and therapeutic applications.
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We claim: 1. A therapeutic composition for detecting or modulating a biological activity of a splice variant polypeptide, comprising a pharmaceutically-acceptable carrier and an antibody or antigen-binding fragment thereof that exhibits binding specificity for an isolated aminoacyl-tRNA synthetase (AARS) splice variant polypeptide that consists of SEQ ID NO: 14, 74, 76, or 78 or an epitope comprising at least 5 amino acids selected from SEQ ID NOs: 55, 57, 69, 182, 194, and 196, wherein the composition has a purity of at least about 90% on a protein basis and less than about 10 EU endotoxin/mg protein. 2. The therapeutic composition of claim 1 , wherein the AARS polypeptide is selected from SEQ ID NO: 14, 74, 76, and 78. 3. The therapeutic composition of claim 1 , wherein the antibody or antigen binding fragment thereof is a monoclonal antibody. 4. The therapeutic composition of claim 1 , wherein the antibody is a humanized antibody. 5. The therapeutic composition of claim 1 , wherein the antibody or antigen-binding fragment thereof is an Fv fragment or a single chain Fv (sFv) polypeptide. 6. The therapeutic composition of claim 1 , wherein the composition is a sterile, freeze-dried powder. 7. The therapeutic composition of claim 1 , wherein the composition is a sterile injectable solution. 8. The therapeutic composition of claim 1 , wherein the composition is buffered and comprises an isotonic agent. 9. The therapeutic composition of claim 1 , wherein the composition is suitable for intravenous, intramuscular, subcutaneous, or intraperitoneal administration. 10. The therapeutic composition of claim 1 , wherein the composition comprises a surfactant. 11. The therapeutic composition of claim 1 , wherein the composition has a purity of at least about 95% on a protein basis.
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