Enzymic Detoxification for Organophosphate Nerve Agents

Information

  • Research Project
  • 7373200
  • ApplicationId
    7373200
  • Core Project Number
    R01GM068550
  • Full Project Number
    2R01GM068550-05
  • Serial Number
    68550
  • FOA Number
    PA-07-70
  • Sub Project Id
  • Project Start Date
    7/1/2003 - 20 years ago
  • Project End Date
    6/30/2012 - 11 years ago
  • Program Officer Name
    IKEDA, RICHARD A.
  • Budget Start Date
    7/17/2008 - 15 years ago
  • Budget End Date
    6/30/2009 - 14 years ago
  • Fiscal Year
    2008
  • Support Year
    5
  • Suffix
  • Award Notice Date
    7/17/2008 - 15 years ago

Enzymic Detoxification for Organophosphate Nerve Agents

[unreadable] DESCRIPTION (provided by applicant): Organophosphate and organophosphonate esters are among the most toxic compounds that have ever been synthesized. These compounds are toxic because of their inherent ability to interfere with nerve transmission through the rapid and irreversible inactivation of the enzyme acetyl cholinesterase. The toxic properties of the organophosphates have been exploited as agricultural insecticides and as chemical weapons. A bacterial phosphotriesterase enzyme has been identified that can function as a catalyst for the recognition, hydrolysis, and detoxification of a broad spectrum of organophosphate nerve agents. The primary objective of this application is to design and characterize modified forms of the bacterial phosphotriesterase that are optimized for the selective recognition and destruction of those organophosphates that pose the most serious threats to human health. Rational and combinatorial libraries of mutant enzymes will be constructed and those variants with enhanced catalytic proficiency will be identified through novel screening and selection procedures. The progressive changes in the amino acid sequence of the bacterial phosphotriesterase will be directly correlated with the enhancements in the catalytic constants and the modifications within the active site as determined by X-ray diffraction methods. PUBLIC HEALTH RELEVANCE: The toxic properties of the organophosphate nerve agents represent a serious threat to the health and well being of civilized societies. The primary objective of this project is to create novel catalytic enzymes that are optimized in their ability to detect, destroy and detoxify a broad spectrum of organophosphate nerve agents. [unreadable] [unreadable] [unreadable]

IC Name
NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
  • Activity
    R01
  • Administering IC
    GM
  • Application Type
    2
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    302007
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    859
  • Ed Inst. Type
    SCHOOLS OF ARTS AND SCIENCES
  • Funding ICs
    NIGMS:302007\
  • Funding Mechanism
  • Study Section
    MSFE
  • Study Section Name
    Macromolecular Structure and Function E Study Section
  • Organization Name
    TEXAS A&M UNIVERSITY SYSTEM
  • Organization Department
    CHEMISTRY
  • Organization DUNS
    047006379
  • Organization City
    COLLEGE STATION
  • Organization State
    TX
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    77845
  • Organization District
    UNITED STATES