TOWARDS A HEAT-LABILE CHELATOR FOR HOT-START PCR

Information

  • Research Project
  • 6294028
  • ApplicationId
    6294028
  • Core Project Number
    R43GM061439
  • Full Project Number
    1R43GM061439-01A1
  • Serial Number
    61439
  • FOA Number
  • Sub Project Id
  • Project Start Date
    5/1/2001 - 24 years ago
  • Project End Date
    10/31/2002 - 23 years ago
  • Program Officer Name
    PREUSCH, PETER C.
  • Budget Start Date
    5/1/2001 - 24 years ago
  • Budget End Date
    10/31/2002 - 23 years ago
  • Fiscal Year
    2001
  • Support Year
    1
  • Suffix
    A1
  • Award Notice Date
    4/27/2001 - 24 years ago

TOWARDS A HEAT-LABILE CHELATOR FOR HOT-START PCR

DESCRIPTION (applicant's abstract): Many PCR analyses, particularly those with rare targets or those with compromised DNA templates (such as forensic analyses), benefit from a hot start. In a normal (room temperature) start, the primers can prime at non-specific sequences, or on each other, during reaction setup. The result can be competitive or inhibitory product produced at the expense of the desired product. In a hot start, a critical component is kept inactive or separate from the reaction until the temperature is at least 65C, at which temperature the primers are properly selective. Current methods of achieving a hot startare tedious, expensive, and/or have shortcomings. We propose to develop heat-labile chelators of Mg++ ion as hot-start reagents for PCR. The DNA polymerases used in PCR reactions are Mg++ dependant, and the Mg++ chelator EDTA inhibits PCR. The ideal hot-start chelator would be stable at room temperature in PCR reaction buffer for at least an hour, but will inactivate and release the Mg++ ion during the first PCR heat cycle, yet not inhibit the PCR reaction itself. To perform hot-start with these reagents, sequestered Mg++ ions (in the form of soluble Mg-chelate) would be added to PCR reactions in place of MgCI2 as a source of Mg++ ions. We propose three lead groups of compounds that have the structural characteristics of Mg++ chelators, and can be inactivated under controlled conditions. PROPOSED COMMERCIAL APPLICATION: Methods for hot-start PCR have proven to be impartant-- even critical-- for many PCR procedures, such as forensic analysis, food and blood product contamination assays. Although most PCR applications benefit from hot-start methods, they are underused because they add significant cost and effort, and they have inadequacies. The labile Mg-chelating reagents we propose to develop and test will be inexpensive, easy to use, and will likely be more effective mediators of hot-start than current methods. They may in fact be inexpensive enough to become standard reagents for PCR used by thousands of laboratories world wide. Such labile chelators may also have applications for other biotechnology and chemical processes.

IC Name
NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
  • Activity
    R43
  • Administering IC
    GM
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    107856
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    821
  • Ed Inst. Type
  • Funding ICs
    NIGMS:107856\
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    DNA POLYMERASE TECHNOLOGY, INC.
  • Organization Department
  • Organization DUNS
    124524989
  • Organization City
    ST. LOUIS
  • Organization State
    MO
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    631041304
  • Organization District
    UNITED STATES