IP Library Granted Patent US 8,981,045
Granted Patent B2
US 8,981,045 · App. 13/696,044 · Granted Mar 17, 2015

Innovative discovery of therapeutic, diagnostic, and antibody compositions related to protein fragments of methionyl-tRNA synthetases

Inventors: Leslie Ann Greene (San Diego, CA); Kyle P. Chiang (Cardiff, CA); Fei Hong (San Diego, CA); Alain Philippe Vasserot (Carlsbad, CA); Jeffry D. Watkins (Encinitas, CA); Cheryl L. Quinn (Minneapolis, MN); Wing-Sze Lo (Chai Wan, HK); John D. Mendlein (Encinitas, CA)
Assignees: aTyr Pharma, Inc.; Pangu BioPharma Limited
C12N9/93C07K16/40C12N5/0602C12N9/96G01N33/68
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,981,045
App. No.
13/696,044
Granted
Mar 17, 2015
Kind
B2
Abstract

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.

Claims (16)

1. A therapeutic composition, comprising an isolated methionyl-tRNA synthetase (MetRS) polypeptide of about 50 to about 100 amino acids in length and comprising an amino acid sequence that is at least 95% identical to SEQ ID NO:137, 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 MetRS polypeptide specifically binds to a binding partner to exert a physiological effect.

3. The therapeutic composition of claim 1 , wherein the MetRS polypeptide consists of SEQ ID NO:137 or differs from SEQ ID NO:137 by substitution, deletion, and/or addition of about 1, 2, or 3 amino acids.

4. The therapeutic composition of claim 1 , wherein the MetRS 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 MetRS polypeptide.

6. The therapeutic composition of claim 1 , wherein the MetRS polypeptide is fused to a pharmacokinetic (PK) property modifier.

7. The therapeutic composition of claim 1 , wherein the MetRS polypeptide consists of SEQ ID NO:137 or differs from SEQ ID NO:137 by substitution, deletion, and/or addition of about 1 or 2 amino acids.

8. The therapeutic composition of claim 1 , wherein the MetRS polypeptide comprises SEQ ID NO:137.

9. The therapeutic composition of claim 1 , wherein the MetRS polypeptide is about 50 to about 80 amino acids in length and comprises SEQ ID NO:137 or a sequence that is at least 95% identical to SEQ ID NO:137.

10. The therapeutic composition of claim 9 , wherein the MetRS polypeptide comprises SEQ ID NO:137.

11. The therapeutic composition of claim 1 , wherein the MetRS polypeptide is about 50 to about 60 amino acids in length and comprises SEQ ID NO:137 or a sequence that is at least 95% identical to SEQ ID NO:137.

12. The therapeutic composition of claim 11 , wherein the MetRS polypeptide comprises SEQ ID NO:137.

13. 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.

14. A method of modulating a cellular activity of a cell, or protein, comprising contacting the cell or protein with the therapeutic composition of claim 1 .

15. The method of claim 14 , 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.

16. The method of claim 15 , wherein the disease is selected from cancer, neuropathy, diabetes, and inflammatory disorders.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 15, 2014
From: GREENE, LESLIE ANN; CHIANG, KYLE P.; HONG, FEI; VASSEROT, ALAIN PHILIPPE; WATKINS, JEFFRY D.; QUINN, CHERYL L.; MENDLEIN, JOHN D.
To: ATYR PHARMA, INC.
Reel/Frame 031977/0679 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 15, 2014
From: LO, WING-SZE
To: PANGU BIOPHARMA LIMITED
Reel/Frame 031977/0774 →
Continuity (3)
Provisional Application 61330596 · May 3, 2010
Provisional Application 61331282 · May 4, 2010
Related Publication 20130236440A1 · Sep 12, 2013