US2020231702A1PendingUtilityA1

Innovative discovery of therapeutic, diagnostic, and antibody compositions related to protein fragments of seryl-trna synthetases

Assignee: ATYR PHARMA INCPriority: May 3, 2010Filed: Nov 21, 2019Published: Jul 23, 2020
Est. expiryMay 3, 2030(~3.8 yrs left)· nominal 20-yr term from priority
C12N 9/93A61P 9/14C07K 16/40A61P 31/04C12Y 601/01011A61K 38/00A61P 11/00A61P 11/06A61P 37/00A61P 27/16A61P 7/00G01N 33/573C07K 2317/24A61P 31/00A61P 25/28A61P 27/02A61P 35/00A61P 9/00A61P 19/10A61P 37/06A61P 3/06A61P 21/00A61P 37/02A61P 43/00A61P 3/10A61P 25/02G01N 2333/9015A61K 9/0019A61P 19/00A61P 29/00A61P 3/00A61P 25/00
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Claims

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

exact text as granted — not AI-modified
1 - 125 . (canceled) 
     
     
         126 . A therapeutic composition, comprising an isolated aminoacyl-tRNA synthetase (AARS) polypeptide that is at least 80%, 85%, 90%, 95%, 98%, or 100% identical to a sequence in any of Table(s) 1-9, wherein the polypeptide 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 and less than about 10 EU endotoxin/mg protein. 
     
     
         127 . The therapeutic composition of  claim 126 , wherein the AARS polypeptide has an extracellular signaling activity. 
     
     
         128 . The therapeutic composition of  claim 126 , wherein the AARS polypeptide consists of an amino acid sequence set forth in any of Table(s) 1-9 or differs from an amino acid sequence set forth in any of Table(s) 1-9 by substitution, deletion, and/or addition of about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, or 11 amino acids. 
     
     
         129 . The therapeutic composition of  claim 126 , wherein the AARS polypeptide is fused to a heterologous polypeptide. 
     
     
         130 . The therapeutic composition of  claim 126 , wherein at least one moiety or a solid substrate is covalently or non-covalently attached to said polypeptide. 
     
     
         131 . An isolated aminoacyl-tRNA synthetase (AARS) polypeptide that is at least 80%, 85%, 90%, 95%, 98%, or 100% identical to an amino acid sequence set forth in any of Table(s) 1-9. 
     
     
         132 . The isolated AARS polypeptide of  claim 131 , wherein the AARS polypeptide is fused to a heterologous polypeptide. 
     
     
         133 . A system, comprising an AARS polypeptide of  claim 131 , and an element selected from the group consisting of:
 (i) a binding partner that binds to the AARS polypeptide;   (ii) an engineered population of cells in which at least one cell comprises a polynucleotide encoding said AARS polypeptide, wherein the cells are capable of growing in a serum-free medium;   (iii) a cell that comprises a cell-surface receptor or an extracellular portion thereof that binds to the polypeptide, and a molecule of less than about 2000 daltons, or a second polypeptide, which modulates binding or interaction of the AARS polypeptide and the extracellular receptor;   (iv) a cell that comprises a cell-surface receptor or an extracellular portion thereof that specifically binds to the AARS polypeptide, wherein the cell comprises an indicator molecule that allows detection of a change in the levels or activity of the cell-surface receptor or extracellular portion thereof; and   (v) an engineered population of cells in which at least one cell comprises a polynucleotide encoding said AARS polypeptide, at least about 10 liters of a serum-free growth medium, and a sterile container.   
     
     
         134 . A method of determining presence or levels of an AARS polypeptide or a polynucleotide that encodes the AARS polypeptide in a sample, comprising:
 (a) contacting the sample with one or more binding agents or antibodies or antigen-binding fragments thereof that specifically bind to an AARS polypeptide of  claim 131 , detecting the presence or absence of the binding agent, and thereby determining the presence or levels of the AARS polypeptide;   (b) analyzing the sample with a detector that is capable of specifically identifying an AARS polypeptide of  claim 131 , and thereby determining the presence or levels of the AARS polypeptide;   (c) contacting the sample with one or more oligonucleotides that specifically hybridize to polynucleotide that encodes an AARS polypeptide of  claim 131 , detecting the presence or absence of the oligonucleotides in the sample, and thereby determining the presence or levels of the polynucleotide; or   (d) contacting the sample with at least two oligonucleotides that specifically amplify a polynucleotide that encodes an AARS polypeptide of  claim 131 , performing an amplification reaction, detecting the presence or absence of an amplified product, and thereby determining presence or levels of the polynucleotide.   
     
     
         135 . A method of modulating a cellular activity of a cell, or protein, comprising contacting the cell or protein with an AARS polypeptide  claim 131 , or a composition comprising a pharmaceutically-acceptable carrier and said AARS polypeptide. 
     
     
         136 . The method of  claim 135 , wherein the cell or protein is in a subject having a disease or disorder optionally mediated by the dysregulation of the expression, activity or spatiotemporal location of a tRNA synthetase, comprising administering the AARS polypeptide or the composition to the subject. 
     
     
         137 . A composition, comprising (a) a binding agent or an antibody or antigen binding fragment thereof that exhibits binding specificity for an AARS polypeptide of  claim 131 , or (b) an isolated polynucleotide that encodes an AARS polypeptide of  claim 131 . 
     
     
         138 . A method of identifying a compound that specifically binds to an AARS polypeptide of  claim 131 , comprising a) combining the AARS polypeptide or its cellular binding partner or both with at least one test compound under suitable conditions, and b) detecting binding of the AARS polypeptide to the test compound, thereby identifying a compound that specifically binds to the AARS polypeptide.

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