IP Library Granted Patent US 9,034,321
Granted Patent B2
US 9,034,321 · App. 13/696,046 · Granted May 19, 2015

Innovative discovery of therapeutic, diagnostic, and antibody compositions related to protein fragments of phenylalanyl-alpha-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
C12N9/93A61K38/53C12Y601/0102C07K16/40C12N5/0602C12N9/96G01N33/68
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Quick Facts
Patent No.
US 9,034,321
App. No.
13/696,046
Granted
May 19, 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 (21)

1. A therapeutic composition, comprising an isolated phenylalanyl-alpha-tRNA synthetase (PheRSa) polypeptide of up to about 240 amino acids in length that comprises SEQ ID NO:45 or an amino acid sequence that is at least 95% identical to SEQ ID NO:45, 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 PheRSa polypeptide specifically binds to a binding partner to exert a physiological effect.

3. The therapeutic composition of claim 1 , wherein the PheRSa polypeptide consists of SEQ ID NO:45 or differs from SEQ ID NO:45 by substitution, deletion, and/or addition of about 1, 2, 3, 4, 5, 6, or 7 amino acids, and wherein the altered polypeptide substantially retains a non-canonical activity of the unaltered polypeptide.

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

6. The isolated PheRSa polypeptide of claim 1 , wherein the PheRSa 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 3 , wherein the PheRSa polypeptide consists of SEQ ID NO:45 or differs from SEQ ID NO:45 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 PheRSa polypeptide comprises SEQ ID NO:45, 12, or 43 or a sequence that is at least 95% identical to SEQ ID NO:45, 12, or 43.

12. The therapeutic composition of claim 11 , wherein the PheRSa polypeptide comprises SEQ ID NO:45, 12, or 43.

13. The therapeutic composition of claim 11 , wherein the PheRSa polypeptide is about 200 to about 240 amino acids in length and comprises SEQ ID NO:45, 12, or 43 or a sequence that is at least 95% identical to SEQ ID NO:45, 12, or 43.

14. The therapeutic composition of claim 13 , wherein the PheRSa polypeptide comprises SEQ ID NO:45, 12, or 43.

15. The therapeutic composition of claim 1 , wherein the PheRSa polypeptide is up to about 220 amino acids in length and comprises SEQ ID NO:45 or 43 or a sequence that is at least 95% identical to SEQ ID NO:45 or 43.

16. The therapeutic composition of claim 15 , wherein the PheRSa polypeptide comprises SEQ ID NO:45 or 43.

17. The therapeutic composition of claim 15 , wherein the PheRSa polypeptide is about 200 to about 220 amino acids in length and comprises SEQ ID NO:45 or 43 or a sequence that is at least 95% identical to SEQ ID NO:45 or 43.

18. The therapeutic composition of claim 17 , wherein the PheRSa polypeptide comprises SEQ ID NO:45 or 43.

19. The therapeutic composition of claim 1 , wherein the PheRSa polypeptide is up to about 160 amino acids in length and comprises SEQ ID NO:45 or a sequence that is at least 95% identical to SEQ ID NO:45.

20. The therapeutic composition of claim 19 , wherein the PheRSa polypeptide comprises SEQ ID NO:45.

21. 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, an Ig G protein that can enable some fusion proteins to penetrate the blood brain barrier.

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 61330828 · May 3, 2010
Provisional Application 61330829 · May 3, 2010
Related Publication 20130195832A1 · Aug 1, 2013