IP Library Granted Patent US 8,946,157
Granted Patent B2
US 8,946,157 · App. 13/696,047 · Granted Feb 3, 2015

Innovative discovery of therapeutic, diagnostic, and antibody compositions related to protein fragments of seryl-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
C12N9/93A61K38/00
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Quick Facts
Patent No.
US 8,946,157
App. No.
13/696,047
Granted
Feb 3, 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 (12)

1. A therapeutic composition, comprising an isolated seryl-tRNA synthetase (SRS) polypeptide of up to about 100 amino acids in length that comprises SEQ ID NO:38 or an amino acid sequence that is at least 95% identical to SEQ ID NO:38, wherein the SRS 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 SRS polypeptide specifically binds to a binding partner to exert a physiological effect.

3. The therapeutic composition of claim 1 , wherein the SRS polypeptide differs from SEQ ID NO:38 by substitution, deletion, and/or addition of about 1 or 2 amino acids, and wherein the altered polypeptide retains an extracellular signaling activity of the unaltered polypeptide.

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

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

7. The therapeutic composition of claim 3 , wherein the SRS polypeptide consists of SEQ ID NO:38 or differs from SEQ ID NO:38 by substitution, deletion, and/or addition of about 1 amino acid.

8. The therapeutic composition of claim 1 , wherein the SRS polypeptide is up to about 60 amino acids in length and comprises SEQ ID NO:38 or a sequence that is at least 95% identical to SEQ ID NO:38.

9. The therapeutic composition of claim 8 , wherein the SRS polypeptide is up to about 60 amino acids in length and comprises SEQ ID NO:38 or 42.

10. The therapeutic composition of claim 8 , wherein the SRS polypeptide is up to about 60 amino acids in length and comprises SEQ ID NO:38.

11. The therapeutic composition of claim 1 , wherein the SRS polypeptide is up to about 90 amino acids in length and comprises SEQ ID NO:38 or a sequence that is at least 95% identical to SEQ ID NO:38.

12. The therapeutic composition of claim 11 , wherein the SRS polypeptide is up about 90 amino acids in length and comprises SEQ ID NO:38 or 40.

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 (4)
Provisional Application 61330826 · May 3, 2010
Provisional Application 61330779 · May 3, 2010
Provisional Application 61330825 · May 3, 2010
Related Publication 20130315887A1 · Nov 28, 2013