Compositions and methods comprising histidyl-TRNA synthetase splice variants having non-canonical biological activities
Isolated histidyl-tRNA synthetase splice variant polynucleotides and polypeptides having non-canonical biological activities are provided, as well as compositions and methods related thereto.
1. A method for treating an inflammatory or autoimmune condition in a subject in need thereof, comprising administering to the subject a pharmaceutical composition that comprises a pharmaceutically acceptable carrier and a histidyl-tRNA synthetase (HRS) polypeptide splice variant, where the HRS polypeptide is about 50-175 amino acids in length and comprises 50 or more contiguous amino acids of SEQ ID NO:6 or a variant thereof having at least 95% sequence identity to SEQ ID NO:6, and where the HRS polypeptide comprises a WHEP domain and lacks a functional aminoacylation domain.
2. The method of claim 1 , where the HRS polypeptide is about 50-70 amino acids in length.
3. The method of claim 2 , where the HRS polypeptide comprises the amino acid sequence of SEQ ID NO:6 or a variant thereof having at least 95% sequence identity to SEQ ID NO:6.
4. The method of claim 3 , where the HRS polypeptide consists essentially of SEQ ID NO:6.
5. The method of claim 1 , where the HRS polypeptide is about 175 amino acids in length.
6. The method of claim 5 , where the HRS polypeptide comprises the amino acid sequence of SEQ ID NO:9 or a variant thereof having at least 95% sequence identity to SEQ ID NO:9.
7. The method of claim 6 , where the HRS polypeptide comprises the amino acid sequence of SEQ ID NO:9.
8. The method of claim 7 , where the HRS polypeptide consists essentially of SEQ ID NO:9.
9. A method for treating an inflammatory or autoimmune condition in a subject in need thereof, comprising administering to the subject a pharmaceutical composition that comprises a pharmaceutically acceptable carrier and a histidyl-tRNA synthetase (HRS) polypeptide, where the HRS polypeptide is about 212 amino acids in length and comprises 50 or more contiguous amino acids of SEQ ID NO:11 or a variant thereof having at least 95% sequence identity to SEQ ID NO:11, and where the HRS polypeptide comprises a WHEP domain and lacks a functional aminoacylation domain.
10. An isolated histidyl-tRNA synthetase (HRS) splice variant polypeptide, for use in a method of reducing inflammatory activity wherein the HRS polypeptide comprises the amino acid sequence of SEQ ID NO: 11, or a variant thereof having at least 95% sequence identity to SEQ ID NO: 11, where the HRS polypeptide comprises a WHEP domain and lacks a functional aminoacylation domain.
11. The method of claim 10 , where the HRS polypeptide comprises the amino acid sequence of SEQ ID NO:11.
12. The method of claim 11 , where the HRS polypeptide consists essentially of SEQ ID NO:11.
13. A method for treating an inflammatory or autoimmune condition in a subject in need thereof, comprising administering to the subject a pharmaceutical composition that comprises a pharmaceutically acceptable carrier and a histidyl-tRNA synthetase (HRS) polypeptide, where the HRS polypeptide is about 40-80 amino acids in length and comprises about 40 or more contiguous amino acids of SEQ ID NO:6 or a variant thereof having at least 95% sequence identity to SEQ ID NO:6 where the HRS polypeptide comprises a WHEP domain.
14. The method of claim 13 , where the HRS polypeptide comprises about 50 or more amino acids of SEQ ID NO:6.
15. The method of claim 13 , where the HRS polypeptide consists essentially of SEQ ID NO:6.
16. A method for treating an inflammatory or autoimmune condition in a subject in need thereof, comprising administering to the subject a pharmaceutical composition that comprises a pharmaceutically acceptable carrier and a histidyl-tRNA synthetase (HRS) polypeptide, where the HRS polypeptide consists essentially of a WHEP domain from human histidyl-tRNA synthetase (HRS).
17. The method of any of claim 1 , 9 , 13 , or 16 , where the HRS polypeptide is modified by pegylation.
18. The method of any of claim 1 , 9 , 13 , or 16 , where the HRS polypeptide further comprises a heterologous fusion partner.
19. The method of claim 18 , where the heterologous fusion partner comprises an Fc fragment.
20. The method of any of claim 1 , 9 , 13 , or 16 , where the HRS polypeptide is a recombinant polypeptide.
21. The method of any of claim 1 , 9 , 13 , or 16 , where the HRS polypeptide is a synthetic polypeptide.
22. The method of any of claim 1 , 9 , 13 , or 16 , where the HRS polypeptide comprises at least one chemical or enzymatic derivation at one or more constituent amino acids where the at least one chemical or enzymatic derivation is selected from acetylation, hydroxylation, methylation, amidation, glycosylation, and lipidation.
23. The method of any of claim 1 , 9 , 13 , or 16 , where the pharmaceutical composition is formulated with histidine.
24. The method of any of claim 1 , 9 , 13 , or 16 , where the pharmaceutical composition comprises a surfactant.
25. The method of any of claim 1 , 9 , 13 , or 16 , where the pharmaceutical composition is administered by oral, parenteral, intravenous, intranasal, inhalation, aerosol, intracranial, or intramuscular administration.
26. An isolated recombinant histidyl-tRNA synthetase (HRS) polypeptide, for use in a method of reducing inflammatory activity wherein the HRS polypeptide is 50-175 amino acids in length and comprises at least 50 contiguous amino acids of SEQ ID NO: 6, or a variant thereof having at least 95% sequence identity to SEQ ID NO: 6, where the HRS polypeptide comprises a WHEP domain and lacks a functional aminoacylation domain.