IP Library Granted Patent US 8,993,723
Granted Patent B2
US 8,993,723 · App. 13/643,753 · Granted Mar 31, 2015

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

Inventors: Leslie Ann Greene (San Diego, CA); Kyle P. Chiang (Cardiff, CA); Fei Hong (San Diego, CA); Alain Philippe Vasserot (Carlsbad, CA); Wing-Sze Lo (Chai Wan, HK); Jeffry Dean Watkins (Encinitas, CA); Cheryl L. Quinn (Minneapolis, MN); John D. Mendlein (Encinitas, CA)
Assignees: aTyr Pharma, Inc.; Pangu BioPharma Limited
C07K16/40A61K38/00C12N9/18C12N9/93G01N33/5008G01N33/68G01N2500/00C12N5/0602C12N9/96
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Quick Facts
Patent No.
US 8,993,723
App. No.
13/643,753
Granted
Mar 31, 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 (11)

1. A therapeutic composition, comprising an isolated alanyl-tRNA synthetase (AlaRS) polypeptide that consists of SEQ ID NO:81 or differs from SEQ ID NO:81 by substitution, deletion, and/or addition of about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12 amino acids, wherein the AlaRS 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 AlaRS polypeptide specifically binds to a binding partner to exert a physiological effect.

3. The therapeutic composition of claim 1 , wherein the AlaRS polypeptide consists of SEQ ID NO:81 or differs from SEQ ID NO:81 by substitution, deletion, and/or addition of about 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 amino acids.

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

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

7. The therapeutic composition of claim 1 , wherein the AlaRS polypeptide consists of SEQ ID NO:81 or differs from SEQ ID NO:81 by substitution, deletion, and/or addition of about 1, 2, 3, 4, or 5 amino acids.

8. The therapeutic composition of claim 1 , wherein the AlaRS polypeptide comprises SEQ ID NO:81 or 142 or a sequence that is at least 95% identical to SEQ ID NO:81 or 142.

9. The therapeutic composition of claim 8 , wherein the AlaRS polypeptide comprises SEQ ID NO:81 or 142.

10. The therapeutic composition of claim 8 , wherein the AlaRS polypeptide comprises SEQ ID NO:81.

11. 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.

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 61328871 · Apr 28, 2010
Provisional Application 61328867 · Apr 28, 2010
Provisional Application 61329048 · Apr 28, 2010
Related Publication 20130287755A1 · Oct 31, 2013