Innovative discovery of therapeutic, diagnostic, and antibody compositions related to protein fragments of tyrosyl-tRNA synthetases
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.
1. A therapeutic composition, comprising an isolated tyrosyl-tRNA synthetase (TyrRS) polypeptide of up to about 260 amino acids in length and comprising an amino acid sequence that is at least 95% identical to SEQ ID NO:34, wherein the polypeptide has an extracellular signaling activity and a solubility of at least about 5 mg/mL, and wherein the composition has a purity of at least about 95% on a protein basis and less than about 10 EU endotoxin/mg protein.
2. The therapeutic composition of claim 1 , wherein the TyrRS polypeptide specifically binds to a binding partner to exert a physiological effect.
3. The therapeutic composition of claim 1 , wherein the TyrRS polypeptide consists of SEQ ID NO:34 or differs from SEQ ID NO:34 by substitution, deletion, and/or addition of about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, or 11 amino acids.
4. The therapeutic composition of claim 1 , wherein the TyrRS polypeptide is fused to a heterologous polypeptide.
5. The therapeutic composition of claim 1 , wherein at least one moiety or a solid substrate is covalently or non-covalently attached to the TyrRS polypeptide.
6. The therapeutic composition of claim 1 , wherein the TyrRS polypeptide is fused to a pharmacokinetic (PK) property modifier.
7. A method of modulating a cellular activity of a cell, or protein, comprising contacting the cell or protein with a therapeutic composition of claim 1 .
8. The method of claim 7 , wherein the cell or protein is in a subject having a disease or disorder mediated by the dysregulation of the expression, activity or spatiotemporal location of a tRNA synthetase, comprising administering the therapeutic composition to the subject.
9. The method of claim 8 , wherein the disease is selected from cancer, neuropathy, diabetes, and inflammatory disorders.
10. The therapeutic composition of claim 1 , wherein the TyrRS polypeptide consists of SEQ ID NO:34 or differs from SEQ ID NO:34 by substitution, deletion, and/or addition of about 1, 2, 3, 4, or 5 amino acids.
11. The therapeutic composition of claim 1 , wherein the TyrRS polypeptide comprises SEQ ID NO:34.
12. The therapeutic composition of claim 6 , wherein the PK modifier is selected from human albumin, antibody Fc domains, poly Glu or poly Asp sequences, transferrin, conformationally disordered polypeptide sequences composed of the amino acids Pro, Ala, and Ser, and IgG.