Chemistry: molecular biology and microbiology – Enzyme – proenzyme; compositions thereof; process for...
Patent
1995-04-21
1997-05-13
Wax, Robert A.
Chemistry: molecular biology and microbiology
Enzyme , proenzyme; compositions thereof; process for...
4352401, 4352523, 43525411, 4353201, 536 232, C12N 900, C12N 120, C12N 114, C07H 2104
Patent
active
056291884
ABSTRACT:
Isolated, recombinant nucleic acids which encode alanyl-tRNA synthetase (AlaRS) of human origin have been used to make expression constructs and transformed host cells for the production of recombinant human AlaRS. The recombinant enzyme has been purified, and is active in the specific aminoacylation of tRNA by alanine. The isolated, recombinant human AlaRS is also recognized by antibodies made by patients with the particular autoimmune disease known as "antisynthetase syndrome" in which the patients produce antibodies against the human alanyl-tRNA synthetase in their own cells. Thus, the isolated, recombinant enzyme, and antibodies made specifically thereto, can be useful in assays to diagnose and monitor this disease. The essential alanyl-tRNA synthetases of microbes pathogenic in humans can be the targets of inhibitory agents having antimicrobial activity. The human alanyl-tRNA synthetase, isolated and purified, can be used to assess the toxic effect in humans of such an inhibitory agent in various biochemical activity assays. This human enzyme can also be expressed in "tester strains," whose cells rely upon the function of the human alanyl-tRNA synthetase for tRNA.sup.Ala charging. Such tester strains can be used to test for any toxic effects of an antimicrobial agent that specifically interacts with the heterologous human AlaRS gene or gene product.
REFERENCES:
patent: 4713337 (1987-12-01), Jasin et al.
patent: 4952501 (1990-08-01), Jasin et al.
patent: 4963487 (1990-10-01), Schimmel et al.
patent: 5484703 (1996-01-01), Raben et al.
Edwards, H., et al., "An E. coli Aminoacyl-tRNA Synthetase Can Substitute for Yeast Mitochondrial Enzyme Function In Vivo," Cell 51:643-649, Nov. 20, 1987.
Racher, K.I., et al., "Expression and Characterization of a Recombinant Yeast Isoleucyl-tRNA Synthetase," The Journal of Biological Chemistry 266(26):17158-17164, Sep. 15, 1991.
von der Haar, F. et al., "Target Directed Drug Synthesis: The Aminoacyl-tRNA Synthetases as Possible Targets," Angew. Chem. Int. Ed., 20(3):217-223 (1981).
Chalker, A.F., et al., "Analysis and Toxic Overexpression in Escherichia coli of a Staphylococcal Gene Encoding Isoleucyl-tRNA Synthetase," Gene, 141:103-108 (1994).
Hughes, J. and Mellows, G., "Interaction of Pseudomonic Acid A with Escherichia coli B Isoleucyl-tRNA Synthetase," Biochem J., 191:209-219 (1980).
Weygand-Durasevic, I., et al., "Yeast Seryl-tRNA Synthetase Expressed in Escherichia coli Recognizes Bacterial Serine-Specific tRNAs in vivo," Eur. J. Biochem., 214:869-877 (1993).
Walter, R. D. and Kuhlow, F., "Parasite-Specific Interaction of N-[4-(4' Nitroanilino)-Phenyl]-S-(.beta.-Carboxyethyl)-Dithiocarbamic Acid-Ester with Arginyl-tRNA-Synthetase from Dirofilaria immitis," Trop. Med. Parasit., 36:230-232 (1985).
Meinnel, T., et al., "Aminoacyl-tRNA Synthetases: Occurrence, Structure, and Function." In tRNA: Structure, Biosynthesis, and Function, Soll, D. and RajBhandary, U., eds. (Washington, DC: American Society for Microbiology), pp. 251-300 (1995).
Hou, Y.-M., and Schimmel, P., "Evidence That a Major Determinant for the Indentify of a Transfer RNA Is Conserved in Evolution," Biochemistry, 28:6800-6804 (1989).
Sequence of Saccharomyces cerevisiae Cytoplasmic Alanyl-tRNA Synthetase Gene, Complete cds, GenBank Accession: U18672 (2 pages). Entered by Ripmaster, T. L. First available Jan. 2, 1995.
Biswas, T., et al., "An Enzyme-Linked Immunosorbent Assay for the Detection and Quantitation of Anti-Jo-1 Antibody in Human Serum," Journal of Immunological Methods, 98:243-248 (1987).
Raben, N., "Improved Assay Using Recombinant Histidyl-tRNA Synthetase," U.S. Department of Commerce National Technical Information Service, Report No. PAT-APPL-8-052 404, filing date: 22 Apr. 1993.
Bunn, C. C., et al., "Autoantibodies Against Alanyl-tRNA Synthetase and tRNA.sup.Ala Coexist and are Associated with Myositis," J. Exp. Med., 163:1281-1291 (1986).
Bunn, C. and Mathews, M. B., "Autoreactive Epitope Defined as the Anticodon Region of Alanine Transfer RNA," Science, 238:1116-1119 (1987).
Herlihy, W. C., et al., "Mass Spectra of Partial Protein Hydrolysates as a Multiple Phase Check for Long Polypeptides Deduced from DNA Sequences: NH.sub.2 -Terminal Segment of Alanine tRNA Synthetase," Proc. Natl. Acad. Sci. USA, 77(11):6531-6535 (1980).
Chang, P. K. and Dignam, J. D., "Primary Structure of Alanyl-tRNA Synthetase and the Regulation of Its mRNA Levels in Bombyx mori," The Journal of Biological Chemistry, 265(34):20898-20906 (1990).
Selbitschka, W., et al., "Characterization of recA Genes and recA Mutants of Rhizobium meliloti and Rhizobium leguminosarum Biovar viciae," Mol. Gen. Genet, 229:86-95 (1991).
Jasin, M. and Schimmel, P., "Deletion of an Essential Gene in Escherichia coli by Site-Specific Recombination with Linear DNA Fragments," J. Bacteriol. 159(2):783-786 (1984).
Edwards, H. and Schimmel, P., "A Bacterial Amber Suppressor in Saccharomyces cerevisiae Is Selectively Recognized by a Bacterial Aminoacyl-tRNA Synthetase," Molecular and Cellular Biology, 10(4):1633-1642 (1990).
Hughes, J., et al., "Inhibition of Isoleucyl-Transfer Ribonucleic Acid Synthetase in Escherichia coli by Pseudomonic Acid," Biochem. J. 176:305-318 (1978), Great Britain.
Putney, S.D., et al., "Primary Structure of a Large Aminoacyl-tRNA Synthetase," Science, 213:1497-1501 (1981).
Sequence of Arabidopsis thaliana Alanyl-tRNA Synthetase Gene. Mireau, H., et al., EMBL Accession No. Z22673 (4 pages). File created May 7, 1993.
Wiesenberger, G., et al., "The Nuclear Gene MRS2 Is Essential for the Excision of Group II Introns from Yeast Mitochondrial Transcripts in Vivo," The Journal of Biological Chemistry, 267(10):6963-6969 (1992).
Targoff, I. N., and Arnett, F. C., "Clinical Manifestations in Patients with Antibody to PL-12 Antigen (Alanyl-tRNA Synthetase)," The American Journal of Medicine 88:241-251 (1990).
Dignam, J.D., et al., "Alanyl-tRNA Synthetase from Escherichia coli, Bombyx mori and Ratus ratus, Existence of Common Structural Features," Eur. J. Biochem., 198:201-210 (1990).
Ripmaster et al. (1995) Proc. Natl. Acad. Sci. USA 92: 4932-4936.
Schimmel et al. (1980) Macromolecules 13: 716-721.
Shiba et al. (1995) Biochemistry 34: 10340-10349.
Ripmaster Tracy L.
Schimmel Paul R.
Shiba Kiyotaka
Cancer Institute, Japanese Foundation for Cancer Research
Cubist Pharmaceuticals, Inc.
Hobbs Lisa J.
Massachusetts Institute of Technology
Wax Robert A.
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