IP Library Granted Patent US 9,399,770
Granted Patent B2
US 9,399,770 · App. 13/877,899 · Granted Jul 26, 2016

Innovative discovery of therapeutic, diagnostic, and antibody compositions related to protein fragments of tryptophanyl-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
C12N9/93A61K38/53C07K16/40C07K2317/21C07K2317/92
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Quick Facts
Patent No.
US 9,399,770
App. No.
13/877,899
Granted
Jul 26, 2016
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 (15)

1. A therapeutic composition, comprising an isolated tryptophanyl-tRNA synthetase (TrpRS) polypeptide of up to 280 amino acids in length that comprises the amino acid sequence of SEQ ID NO: 56 or an amino acid sequence that is at least 95% identical to the amino acid sequence of SEQ ID NO: 56, wherein the TrpRS polypeptide has an extracellular signaling activity and has 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 as measured by HPLC and less than about 10 EU endotoxin/mg protein.

2. The therapeutic composition of claim 1 , wherein the TrpRS polypeptide consists of the amino acid sequence of SEQ ID NO: 56 or differs from the amino acid sequence of SEQ ID NO: 56 by substitution, deletion, and/or addition of 1, 2, 3, 4, 5, 6, or 7 amino acids.

3. The therapeutic composition of claim 2 , wherein the TrpRS polypeptide consists of the amino acid sequence of SEQ ID NO: 56 or differs from the amino acid sequence of SEQ ID NO:56 by substitution, deletion, and/or addition of 1, 2, or 3 amino acids.

4. The therapeutic composition of claim 1 or 2 , wherein the TrpRS polypeptide is fused to a heterologous polypeptide and retains the extracellular signaling activity.

5. The therapeutic composition of claim 1 or 2 , wherein the TrpRS polypeptide is fused to a heterologous pharmacokinetic (PK) modifier and retains the extracellular signaling activity.

6. The therapeutic composition of claim 1 , wherein at least one heterologous moiety or a heterologous solid substrate is covalently or non-covalently attached to the TrpRS polypeptide and retains the extracellular signaling activity.

7. The therapeutic composition of claim 1 , wherein the TrpRS polypeptide of up to 280 amino acids in length comprises the amino acid sequence of SEQ ID NO:56, 16, or 48 or an amino acid sequence that is at least 95% identical to the amino acid sequence of SEQ ID NO: 56, 16, or 48.

8. The therapeutic composition of claim 7 , wherein the TrpRS polypeptide of up to 280 amino acids in length comprises the amino acid sequence of SEQ ID NO: 56, 16, or 48.

9. The therapeutic composition of claim 1 , wherein the TrpRS polypeptide is up to 260 amino acids in length and comprises the amino acid sequence of SEQ ID NO:56 or 16 or an amino acid sequence that is at least 95% identical to the amino acid sequence of SEQ ID NO: 56 or 16.

10. The therapeutic composition of claim 9 , wherein the TrpRS polypeptide of up to 260 amino acids in length comprises the amino acid sequence of SEQ ID NO: 56 or 16.

11. The therapeutic composition of claim 1 , wherein the TrpRS polypeptide is up to 160 amino acids in length and comprises the amino acid sequence of SEQ ID NO: 56 or an amino acid sequence that is at least 95% identical to the amino acid sequence of SEQ ID NO: 56.

12. The therapeutic composition of claim 11 , wherein the TrpRS polypeptide of up to 160 amino acids in length comprises the amino acid sequence of SEQ ID NO:56.

13. 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 .

14. The method of claim 13 , 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 of claim 1 to the subject.

15. The method of claim 14 , wherein the disease or disorder is selected from cancer, neuropathy, diabetes, and inflammatory disorders.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 27, 2016
From: LO, WING-SZE
To: PANGU BIOPHARMA LIMITED
Reel/Frame 037598/0215 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 27, 2016
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 037598/0354 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 15, 2014
From: LO, WING-SZE
To: PANGU BIOPHARMA LIMITED
Reel/Frame 031977/0745 →
Continuity (4)
Provisional Application 61390555 · Oct 6, 2010
Provisional Application 61390554 · Oct 6, 2010
Provisional Application 61390553 · Oct 6, 2010
Related Publication 20130330312A1 · Dec 12, 2013