Organic compounds -- part of the class 532-570 series – Organic compounds – Carbohydrates or derivatives
Reexamination Certificate
2007-05-29
2007-05-29
Slobodyansky, Elizabeth (Department: 1652)
Organic compounds -- part of the class 532-570 series
Organic compounds
Carbohydrates or derivatives
C536S023400, C435S226000
Reexamination Certificate
active
11488340
ABSTRACT:
Truncated aggrecanase proteins and nucleotides sequences encoding them as well as processes for producing them are disclosed. Additionally, aggrecanases with amino acid mutations that lead to increased stability and expression levels in comparison with wild-type or native aggrecanases are also disclosed. Aggrecanases of the invention are especially useful for development of compositions for treatment of diseases such as osteoarthritis. Methods for developing inhibitors of the aggrecanase enzymes and antibodies to the enzymes for treatment of conditions characterized by the degradation of aggrecan are also disclosed.
REFERENCES:
patent: 4419446 (1983-12-01), Howley et al.
patent: 4816567 (1989-03-01), Cabilly et al.
patent: 6326162 (2001-12-01), Miller et al.
patent: 6391610 (2002-05-01), Apte et al.
patent: 6451575 (2002-09-01), Arner et al.
patent: 6521436 (2003-02-01), Arner et al.
patent: 0123289 (1984-10-01), None
patent: 0155476 (1985-09-01), None
patent: 0177343 (1986-09-01), None
patent: 86/00639 (1986-01-01), None
patent: 99/05291 (1999-02-01), None
patent: 00/53774 (2000-09-01), None
patent: 03/062263 (2003-07-01), None
patent: 2004/011637 (2004-02-01), None
Abbaszade et al., “Cloning . . . ”,JBC, vol. 274 (No. 33), p. 23443-23450, (Aug. 13, 1999).
Altschul et al., “Basic . . . ”,J. Mol. Biol., vol. 215, p. 403-410, (Oct. 5, 1990).
Ausubel, Wiley & Sons,Current Protocols in Molecular Biology, N.Y., 6.3.1-6.3.6, (1989).
Brandt and Mankin, “Pathogenesis . . . ”,Textbook of Rheumatology, WB Saunders, P.A., p. 1355-1373, (1993).
Clackson et al., “Making . . . ”,Nature, vol. 352, p. 624-628, (Aug. 15, 1991).
Flannery et al., “Identification . . . ,”JBC, vol. 267 (No. 2), p. 1008-1014, (Jan. 15, 1992).
Fosang et al., “Neutrofil . . . ”,Biochem. J., vol. 304, p. 347-351, (Dec. 1, 1994).
Gething and Sambrook, “Cell-surface . . . ”,Nature, vol. 293, p. 620-625, (Oct. 22, 1981).
Gossen and Bujard, “Tight . . . ”,PNAS USA, vol. 89, p. 5547-5551, (Jun. 15, 1992).
Gough et al., “Structure . . . ”,EMBO J., vol. 4 (No. 3), p. 645-653, (Mar. 1985).
Hughes et al., “Monoclonal . . . ”,Biochem. J., vol. 305, p. 799-804, (Feb. 1, 1995).
Jang et al., “Initiation . . . ”,J. of Virol., vol. 63 (No. 4), p. 1651-1660, (Apr. 1989).
Kaufman and Sharp, “Amplification . . . ”,J. Mol. Biol., vol. 159, p. 601-621, (Aug. 25, 1982).
Kaufman et al., “Coamplification . . . ”,Mol. and Cellular Bio., vol. 5 (No. 7), p. 1750-1759, (Jul. 1985).
Kaufman and Sharp, “Construction . . . ”,Mol. and Cellular Bio., vol. 2 (No. 11), p. 1304-1319, (Nov. 1982).
Kaufman, “Identification . . . ”,PNAS USA, vol. 82, p. 689-693, (Feb. 1985).
Kaufman et al., “Improved . . . ”,Nuc. Acids Res., vol. 19 (No. 16 ), p. 4485-4490, (Aug. 25, 1991).
Kohler and Milstein, “Continuous . . . ”,Nature, vol. 256, p. 495-497, (Aug. 7, 1975).
Laemmli, “Cleavage . . . ”,Nature, vol. 227, p. 680-685, (Aug. 15, 1970).
Lohmander et al., “The Structure . . . ”,Arthritis&Rheumatism, vol. 36 (No. 9), p. 1214-1222, (Sep. 1993).
Maclean et al., “Costs . . . ”,J. of Rheumatology, vol. 25 (No. 11), p. 2213-2218, (Nov. 1998).
Maniatis et al.,Molecular Cloning: A Laboratory Manual, p. 387-389, (1982).
Marks et al., “By-passing . . . ”,J. Mol. Biol., vol. 222, p. 581-597, (Dec. 5, 1991).
Mercuri et al., “Recombinant . . . ”,JBC, vol. 274 (No. 45), p. 32387-32395, (Nov. 5, 1999).
Miller et al., “An Insect . . . ”,Genetic Engineering, vol. 8, Plenum Press, p. 277-298, (1986).
Morinaga et al., “Improvement . . . ”,Bio/Technology, 84, p. 636-639, (Jul. 1984).
Needleman and Wunsch, “A General . . . ”,J. Mol. Biol., vol. 48, p. 443-453, (Mar. 1970).
Oakley et al., “A Simplified . . . ”,Analytical Biochemistry, vol. 105, p. 361-363, (Jul. 1, 1980).
Okayama and Berg, “High-Efficiency . . . ”,Mol. and Cellular Bio., vol. 2 (No. 2), p. 161-170, (Feb. 1982).
Sandy et al., “Catabolism . . . ”,JBC, vol. 266 (No. 14), p. 8683-8685, (May 15, 1991).
Sandy et al., “The Structure . . . ”,J. Clin. Invest., vol. 89, p. 1512-1516, (May 1992).
Steele et al., “Expression . . . ”,Protein Engineering, vol. 13 (No. 6), p. 397-405, (Jun. 2000).
Taniguchi et al., “Expression . . . ”,PNAS USA, vol. 77 (No. 9), p. 5230-5233, (Sep. 1980).
Tortorella et al., “Purification . . . ”,Science, vol. 284, p. 1664-1666, (Jun. 4, 1999).
Towbin et al., “Electrophoretic . . . ”,PNAS USA, vol. 76 (No. 9), p. 4350-4354, (Sep. 1979).
Urlaub and Chasin, “Isolation . . . ”,PNAS USA, vol. 77 (No. 7), p. 4216-4220, (Jul. 1980).
Wong et al., “Human . . . ”,Science, vol. 228 (No. 4701), p. 810-815, (May 17, 1985).
Cal, Santiago et al., “Cloning Expression Analysis . . . ”,Gene, vol. 283, 2002, pp. 49-62.
Cal, Santiago et al., “Identification, Characterization, and . . . ”,The Journal of Biological Chemistry and Molecular Biology, Inc., vol. 276, No. 21, May 25, 2001, pp. 17932-17940.
Caterson, Bruce et al., “Mechanisms Involved in Cartilage . . . ”,Matrix Biology, vol. 19, 2000, pp. 333-344.
Clark, Melody et al., “ADAMTS9, A Novel Member . . . ”,Genomics, vol. 67, 2000, pp. 343-350.
Flannery, Carl et al., “Autocatalytic Cleavage of AMAMTS-4 . . . ”,The Journal of Biological Chemistry, vol. 277, No. 45, Nov. 8, 2002, pp. 42775-42780.
Gao, Gui et al., “Activation of the Proteolytic . . . ”,The Journal of Biological Chemistry, vol. 277, Mar. 29, 2002, No. 13, pp. 11034-11041.
Hashimoto, Gakuji et al., “Inhibition of ADAMSTS4 (Aggrecanase-1) . . . ”,Federation of European Biochemical Societies, vol. 494, 2001, pp. 192-195.
Hurskainen, Tina et al., “ADAM-TS5, ADAM-TS6 and . . . ”,The Journal of Biological Chemistry, vol. 274, No. 36, Sep. 3, 1999, pp. 25555-25563.
Kuno, Kouji et al., “ADAMTS-1 Protein Anchors at the . . . ”,The Journal of Biological Chemistry, vol. 273, No. 22, May 29, 1988, pp. 13912-13917.
Rodriguez-Manzaneque, Juan Carlos et al., “Characterization of METH-1/ADAMTS1 . . . ”,The Journal of Biological Chemistry, vol. 275, No. 43, Oct. 27, 2000, pp. 33471-33479.
Somerville, Robert et al., “Characterization of ADAMTS-9 . . . ”,The Journal of Biological Chemistry, vol. 278, No. 11, Mar. 14, 2003, pp. 9503-9513.
Tortorella, Micky et al., “The Thrombospondin Motif of Aggrecanase-1 . . . ”,The Journal of Biological Chemistry, vol. 275, No. 33, Aug. 18, 2000, pp. 25791-25797.
Vazquez, Francisca et al., “Meth-1, A Human Ortholog . . . ”,J. Biol. Chem., vol. 274, No. 33, Aug. 13, 1999, pp. 23349-23357.
Myers, E.W. and Miller, W., “Optical alignments in linear space”,CABIOS, 4(1):11-17 (1988).
Harlow, E. and Lane, D.,Antibodies: A Laboratory Manual, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York (1988).
Kuno et al., “ADAMTS-1 Is an Active Metalloproteinase Associated with the Extracellular Matrix”,J. Biol. Chem., 274(26):18821-18826, 1999.
Kashiwagi et al., “Altered proteolytic activities of ADAMTS-4 expressed by C-terminal processing”,J. Biol. Chem., 279(11):10109-10119 (2004).
“Partial European Search Report” of Nov. 16, 2005, European Patent Application 03710886.7.
“International Search Report” of Apr. 30, 2004, International Application PCT/US03/03554.
Collins-Racie Lisa A.
Corcoran Christopher J.
Crawford Tara K.
Freeman Bethany A.
Georgiadis Katy E.
Kirkpatrick & Lockhart Preston Gates & Ellis LLP
Slobodyansky Elizabeth
Wyeth
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