IP Library Granted Patent US 9,404,104
Granted Patent B2
US 9,404,104 · App. 14/689,925 · Granted Aug 2, 2016

Innovative discovery of therapeutic, diagnostic, and antibody compositions related to protein fragments of P38 multi-tRNA synthetase complex

Inventors: Leslie Ann Greene (San Diego, CA); Kyle P. Chiang (Cardiff, CA); Alain P. Vasserot (Carlsbad, CA); Jeffry D. Watkins (Encinitas, CA); Cheryl L. Quinn (Minneapolis, MN); John D. Mendlein (Encinitas, CA)
Assignee: aTyr Pharma, Inc.
C12N9/93A61K38/53C07K16/40C12N5/0602C12N9/96G01N33/573G01N33/68C07K2317/92C12Y601/01G01N2333/9015
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 9,404,104
App. No.
14/689,925
Granted
Aug 2, 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 (9)

1. A pharmaceutical composition comprising a pharmaceutically-acceptable carrier and a modified mRNA polynucleotide that encodes an isolated p38 polypeptide of 80 to 150 amino acids in length and comprising an amino acid sequence that is at least 95% identical to SEQ ID NO: 12 or 14, wherein the p38 polypeptide has an extracellular signaling activity, and wherein the composition is substantially endotoxin-free.

2. The pharmaceutical composition of claim 1 , wherein the AARS polypeptide consists of SEQ ID NO:12 or 14 or differs from SEQ ID NO:12 or 14 by substitution, deletion, and/or addition of 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10 amino acids.

3. The pharmaceutical composition of claim 1 , wherein the modified mRNA polynucleotide is at least 95% identical to SEQ ID NO:13 or 15.

4. The pharmaceutical composition of claim 1 , wherein the modified mRNA polynucleotide comprises one or more transcriptional and/or translational control elements.

5. The pharmaceutical composition of claim 1 , wherein the modified mRNA polynucleotide comprises at least one modified base.

6. The pharmaceutical composition of claim 1 , wherein the isolated polynucleotide is formulated for delivery encapsulated in a lipid particle, a liposome, a vesicle, a nanosphere, or a nanoparticle.

7. The pharmaceutical composition of claim 1 , which is suitable for intravenous administration.

8. The pharmaceutical composition of claim 1 , wherein the p38 polypeptide is fused to a heterologous polypeptide.

9. The pharmaceutical composition of claim 8 , wherein the heterologous polypeptide is selected from the group consisting of purification tags, epitope tags, targeting sequences, signal peptides, membrane translocating sequences, and pharmacokinetic (PK) property modifiers.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 27, 2015
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 036439/0217 →
Continuity (5)
Continuation 13696049
Provisional Application 61331065 · May 4, 2010
Provisional Application 61331063 · May 4, 2010
Provisional Application 61331066 · May 4, 2010
Related Publication 20150361413A1 · Dec 17, 2015