MICRODETECTION TECHNOLOGY FOR AUTOMATED DNA SEQUENCING

Information

  • Research Project
  • 3333907
  • ApplicationId
    3333907
  • Core Project Number
    R01HG000776
  • Full Project Number
    5R01HG000776-02
  • Serial Number
    776
  • FOA Number
    RFA-HG-92-201
  • Sub Project Id
  • Project Start Date
    9/25/1992 - 31 years ago
  • Project End Date
    7/31/1994 - 29 years ago
  • Program Officer Name
  • Budget Start Date
    9/1/1993 - 30 years ago
  • Budget End Date
    7/31/1994 - 29 years ago
  • Fiscal Year
    1993
  • Support Year
    2
  • Suffix
  • Award Notice Date
    8/30/1993 - 30 years ago

MICRODETECTION TECHNOLOGY FOR AUTOMATED DNA SEQUENCING

DESCRIPTION: (Adapted from the applicant's abstract) This proposal outlines plans for the development of a new microdetection technique, which is to be coupled with the SBH method. The specific aims to achieve the potential benefits of the proposed sequencing approach are categorized into microdetection technology development and transfer tasks consisting of the following components. Device development includes the design, fabrication, testing, and evaluation of microchips for directly detecting the hybridization of target DNA to probe DNA attached on interdigitated electrodes arrayed on a microfabricated substrate. Each electrode in the hybridization array is activated by an alternating electric field to detect variations in local dielectric properties to signify the presence of hybridized target DNA, thereby revealing the oligonucleotide content of the sample DNA under test. Device modeling entails the mathematical modeling of the biologic/electronic interface to enable calculation of the detection sensitivity of the devices. A Gouy-Chapman electrical double-layer model will be formulated with varying charge concentrations near the surface to represent the attached DNA probes. An equivalent electrical circuit model will then be derived to sufficiently describe the interface for sensitivity calculations. Surface chemistry involves developing a rapid, efficient method for attaching the oligonucleotide probes to the gold microelectrodes on the array. A three-step procedure outlined involves activation of the gold support with a dithiodecane linker, followed by activation of amine- modified oligonucleotides, and a final linker/probe coupling reaction. Surface chemistry also includes the specificity analysis of hybridization conducted directly in the micro-miniature test wells embedded within the micro-fabricated array. Technology transfer is addressed by the formation of a research consortium early in the research phase to effect efficient transfer of the proposed microdetection technology to industry. The Genosensor Consortium, to be composed of industry, academia, and government, will be formulated to develop and commercialize promising technology.

IC Name
NATIONAL HUMAN GENOME RESEARCH INSTITUTE
  • Activity
    R01
  • Administering IC
    HG
  • Application Type
    5
  • 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
    SRC
  • Study Section Name
  • Organization Name
    HOUSTON ADVANCED RESEARCH CENTER
  • Organization Department
  • Organization DUNS
  • Organization City
    THE WOODLANDS
  • Organization State
    TX
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    77381
  • Organization District
    UNITED STATES