DNA SEQUENCING BY ELECTROSPRAY AND ION/ION CHEMISTRY

Information

  • Research Project
  • 2761362
  • ApplicationId
    2761362
  • Core Project Number
    R21HG001887
  • Full Project Number
    1R21HG001887-01
  • Serial Number
    1887
  • FOA Number
  • Sub Project Id
  • Project Start Date
    2/1/1999 - 25 years ago
  • Project End Date
    1/31/2001 - 23 years ago
  • Program Officer Name
    GRAHAM, BETTIE
  • Budget Start Date
    2/1/1999 - 25 years ago
  • Budget End Date
    1/31/2000 - 24 years ago
  • Fiscal Year
    1999
  • Support Year
    1
  • Suffix
  • Award Notice Date
    1/19/1999 - 25 years ago

DNA SEQUENCING BY ELECTROSPRAY AND ION/ION CHEMISTRY

DESCRIPTION (Adapted from the Investigator's Abstract): The objective of this proposal is to develop methodology for high speed DNA sequencing that can yield sequence data roughly two orders of magnitude faster than current state-of-the-art technology, with comparable or superior accuracy. Specifically, the goal is to provide full sequence information on DNA stands consisting of at least 500 bases in seconds to minutes. The proposed approach is based on electrospray ionization/quadrupole ion trap mass spectrometry employing gas-phase ion/ion chemistry. Electrospray has been shown to be capable of yielding gas-phase ions of nucleic acid oligomers extending far in excess of 500 bases. However, electrospray-based approaches for high speed DNA sequencing have not been extensively pursued due to spectral congestion associated with multiple charging phenomenon that is characteristic of electrospray. The formation of multiple charge states from a single oligomer severely limits the mixture complexity amenable to direct analysis via electrospray. For this reason, electrospray usually follows a separation method, such as liquid chromatography or capillary electrophoresis, when applied to mixtures. The investigators have demonstrated that proton transfer reactions resulting from the interaction of oppositely-charged ions in a quadrupole ion trap is a robust means for greatly reducing the spectral congestion associated with mixtures of biopolymers. They present evidence that the combination of electrospray and ion/ion chemistry is highly promising as a core element in a strategy for high speed DNA sequencing. This strategy involves the generation of oligonucleotide mixtures via the Sanger method and direct analysis of these mixtures with electrospray combined with ion/ion chemistry. The output of this procedure is analogous to that produced via conventional electrophoresis-based sequencing technologies wherein the time-scale is replaced by a mass scale. Depending upon the nature of the as yet unknown limiting factors for this approach, the read length might reach as high as several thousand bases.

IC Name
NATIONAL HUMAN GENOME RESEARCH INSTITUTE
  • Activity
    R21
  • Administering IC
    HG
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    172
  • Ed Inst. Type
  • Funding ICs
  • Funding Mechanism
  • Study Section
    GNM
  • Study Section Name
    Genome Study Section
  • Organization Name
    LOCKHEED MARTIN ENERGY RESEARCH CORP
  • Organization Department
  • Organization DUNS
  • Organization City
    OAK RIDGE
  • Organization State
    TN
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    37831
  • Organization District
    UNITED STATES