OP-1 3D STRUCTURE USED IN DRUG DESIGN FOR BONE DISORDERS

Information

  • Research Project
  • 2006679
  • ApplicationId
    2006679
  • Core Project Number
    R43AR044140
  • Full Project Number
    1R43AR044140-01A1
  • Serial Number
    44140
  • FOA Number
  • Sub Project Id
  • Project Start Date
    12/20/1996 - 27 years ago
  • Project End Date
    12/31/1997 - 26 years ago
  • Program Officer Name
  • Budget Start Date
    12/20/1996 - 27 years ago
  • Budget End Date
    12/31/1997 - 26 years ago
  • Fiscal Year
    1997
  • Support Year
    1
  • Suffix
    A1
  • Award Notice Date
    12/19/1996 - 27 years ago

OP-1 3D STRUCTURE USED IN DRUG DESIGN FOR BONE DISORDERS

Abstract of Research Plan: This project will determine the high resolution three dimensional structure (3DS) of OP-1 to atomic resolution and use this structure to design small molecules or peptidomimetic agents for treating osteoporosis and other metabolic bone disease. The synergistic relationship between the most advanced techniques of 3DS analysis and biotechnology will be utilized to work toward effective drug development. Large quantities of recombinant OP-1 expressed in Chinese Hamster Ovary cells have been purified, renatured and examined by gel electropohoresis and HPLC to ensure homogeneity. Biologically active OP-1 has been used to grow crystals for single crystal x-ray diffraction studies and the 3DS solved to 2.8 A resolution. Parts of this structure remain poorly defined and the accuracy of the present model limits our ability to use sophisticated structure guided drug design techniques. Nonetheless, some inferences about the 3DS and potential receptor binding sites have been made, and some potential peptides of interest have been identified. In the proposed project, the high resolution structure studies would be pursued while these initial peptides are synthesized and tested for receptor binding and biological activity in OP-1 assays. In phase I, the OP-1 crystals will be used to determine the 3DS of OP-1 to atomic resolution at reduced temperatures. The atomic model of OP-1 determined the at 2.8 A will be used to extend the 2.9 A x-ray structure to a resolution of 2.0A. Low temperature x-ray data will be collected to define the portions of the structure that were poorly defined in the 2.8A structure and to complete the refinement at 2.0A. Analysis of the x-ray structure with computational programs and detailed comparison with other growth factors will be used to select and synthesize potential active peptides. These peptides will be tested for receptor binding. Those peptides that show significant receptor binding will then be tested in bioassays for agonist and antagonist activity. The information gained from the peptides will be correlated with the 3DS to design lead compounds for the development of potential non-protein based therapeutic agents.

IC Name
NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES
  • Activity
    R43
  • Administering IC
    AR
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    846
  • Ed Inst. Type
  • Funding ICs
  • Funding Mechanism
  • Study Section
    ZRG3
  • Study Section Name
  • Organization Name
    CREATIVE BIOMOLECULES, INC.
  • Organization Department
  • Organization DUNS
  • Organization City
    HOPKINTON
  • Organization State
    MA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    01748
  • Organization District
    UNITED STATES