G-coupled receptor showing selective affinity for ATP

Chemistry: molecular biology and microbiology – Measuring or testing process involving enzymes or... – Involving antigen-antibody binding – specific binding protein...

Reexamination Certificate

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C436S501000

Reexamination Certificate

active

10976678

ABSTRACT:
The present invention relates to an isolated G-protein coupled receptor, nucleic acid sequence encoding the receptor, and host cells capable of expressing the receptor. The invention further comprises methods for detecting the expression of a G-protein coupled receptor, and methods for identifying agonists or antagonists of the receptor. The invention still further encompasses methods for preparing an isolated G-protein coupled receptor.

REFERENCES:
patent: 5981223 (1999-11-01), Sathe et al.
patent: 6114127 (2000-09-01), Bergsma et al.
Jiang et al. Extracellular ATP Triggers Cyclic AMP-Dependent Differentiation of HL-60 Cells, (Mar. 27, 1997), BBRC 232:626-630.
Owicki et al. Continuous Monitoring of Receptor-Mediated Changes in the metabolic Rates of Living Cells, (1990), P.N.A.S. 87:4007-4011.
Cowen et al. Chronic Treatment With P2-Purinergic Receptor Agonists Induces Phenotypic Modulation of the HL-60 and U937 Human Myelogenous Leukemia Cell Lines, (1991), J. of Leukoc. Biol. 50:109-122.
Communi D. & Boeynaems J.M., Receptors responsive to extracellular pyrimidine nucleotides, Mar. 1997, TIPS, vol. 18, pp. 83-86.
Communi D. et al, Cloning of a Human Purinergic P2Y Receptor Coupled to Phospholipase C and Adenyl Cyclase, Dec. 1997, The Journal of Biological Chemistry, vol. 272 No. 51, pp. 31969-31973.
J.A. Parsons, M.A., B.M., B.Ch., Peptide Hormones, University Park Press, Jun. 1976.
Genbank Accession No. AA321112 entered Apr. 19, 1997.
Genbank Accession No. N34073 entered Jan. 11, 1996.
Hammer, et al., 1990, Spontaneous Inflammatory Disease in Transgenic Rats Expressing HLA-B27 and Human B2m: An Animal Model of HLA-B27-Associated Human Disorders, Nov. 30, 1990, Cell Press, vol. 63, 1099-1112.
John J. Mullins, Linda, J. Mullins, Transgenesis in Nonmurine Species, Oct. 1993, Hypertension, vol. 22, No. 4.
Moreadith and Radford (J. Mol. Med. 75:208-216, 1997).
Seamark, Reprod. Fertil. Dev. 6: 653-657, 1994.
Cameron ER. Molecular Biotechnology 7:253-265, 1997.
Gardner RL and Brook FA. International J. of Dev. Biol. 41:235-243, 1997.
Mullins LJ and Mullins JJ. J. Clin. Invest.97:1557-1560, 1996.
Prelle, et al. (Anat Histol Embryol 31:169-186, 2002.
Communi D. & Boeynaems J.M., Receptors responsive to extracellular pyrimidine nucleotides, Mar. 1997, TIPS, vol. 18, pp. 83-86.
Communi D. et al, Cloning of a Human Purinergic P2Y Receptor Coupled to Phospholipase C and Adenyl Cyclase, Dec. 1997, The Journal of Biological Chemistry, vol. 272 No. 51, pp. 31969-31973.
J.A. Parsons, M.A., B.M., B.Ch., Peptide Hormones, University Park Press, Jun. 1976.
Genbank Accession No. AA321112, Apr. 19, 1997.
Genbank Accession No. N34073, Jan. 11, 1996.
Hammer, et al., 1990, Spontaneous Inflammatory Disease in Transgenic Rats Expressing HLA-B27 and Human B2m: An Animal Model of HLA-B27-Associated Human Disorders, Nol. 30, 1990, Cell Press, vol. 63, 1099-1112.
John J. Mullins, Linda J. Mullins, Transgenesis in Nonmurine Species, Oct. 1993, Hypertension, vol. 22, No. 4.

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