Conformational changes in the ACh binding protein

Information

  • Research Project
  • 6894678
  • ApplicationId
    6894678
  • Core Project Number
    F32GM067494
  • Full Project Number
    5F32GM067494-03
  • Serial Number
    67494
  • FOA Number
  • Sub Project Id
  • Project Start Date
    6/5/2003 - 21 years ago
  • Project End Date
    12/4/2005 - 19 years ago
  • Program Officer Name
    STEWART, RANDALL R
  • Budget Start Date
    6/5/2005 - 19 years ago
  • Budget End Date
    12/4/2005 - 19 years ago
  • Fiscal Year
    2005
  • Support Year
    3
  • Suffix
  • Award Notice Date
    5/18/2005 - 19 years ago
Organizations

Conformational changes in the ACh binding protein

[unreadable] DESCRIPTION (provided by applicant): The nicotinic acetylcholine receptor has served as the model member of a large superfamily of neurotransmitter-gated ion channels. However, the atomic structural details of this receptor and its cousins has escaped study due to the receptors large size and amphipathic nature. Recently, a crystal structure has been solved of an acetylcholine binding protein AChBP that possesses structural similarity to nicotinic receptors, but does not have a domain that conducts ions through the membrane. The biochemical and functional properties of this new protein have not been elucidated. Using fluorescent and electrophysiological techniques, this proposal will seek to determine if the acetylcholine binding protein serves as a functional analog as well as a structural analog of the nicotinic receptor. Fluorescent labels will be used to determine if the AChBP undergoes changes in conformation and functional state in a manner analogous to the nicotinic receptor. In addition, the AChBP will be spliced to the ion-conducting regions of a neurotransmitter-gated ion channel to determine if it is capable of eliciting ionic currents when exposed to agonist. The experiments proposed will determine if the the AchBP provides a model for receptor function as well as its structure, and may provide insights into the shape of the binding site of this large and important receptor family. [unreadable] [unreadable]

IC Name
NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
  • Activity
    F32
  • Administering IC
    GM
  • Application Type
    5
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    22524
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    859
  • Ed Inst. Type
  • Funding ICs
    NIGMS:22524\
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    PASTEUR INSTITUTE
  • Organization Department
  • Organization DUNS
  • Organization City
    PARIS CEDEX 15
  • Organization State
  • Organization Country
    FRANCE
  • Organization Zip Code
    75724
  • Organization District
    FRANCE