Fluorescent, Photolabile Terminators for DNA Sequencing

Information

  • Research Project
  • 6834483
  • ApplicationId
    6834483
  • Core Project Number
    R43HG003443
  • Full Project Number
    1R43HG003443-01
  • Serial Number
    3443
  • FOA Number
  • Sub Project Id
  • Project Start Date
    9/20/2004 - 20 years ago
  • Project End Date
    5/19/2005 - 19 years ago
  • Program Officer Name
    SCHLOSS, JEFFERY
  • Budget Start Date
    9/20/2004 - 20 years ago
  • Budget End Date
    5/19/2005 - 19 years ago
  • Fiscal Year
    2004
  • Support Year
    1
  • Suffix
  • Award Notice Date
    9/20/2004 - 20 years ago
Organizations

Fluorescent, Photolabile Terminators for DNA Sequencing

[unreadable] DESCRIPTION (provided by applicant): New methods for sequencing genornic DNA rapidly and accurately in a large number of individuals are needed to better understand the role of genetic variation in common disease. Sequencing-by-synthesis (SBS) is one of the most promising contemporary methods for fast, high-throughput, and low cost genomic DNA sequencing applications. The Base Addition Sequence Scheme (BASS) involves the repetitive cycles of incorporation of 3'-O-labile nucleotide terminators, in situ identification of the incorporated base, and deprotection to yield a 3'-OH group to allow the next cycle of DNA synthesis. The use of DNA templates attached to a solid support eliminates the need for electrophoresis, which resolves the nested DNA fragments by their respective size. We anticipate that formatting the sequencing chemistry into a high density array will increase throughput of the technology, shorten the time required to effect the examination, and lower the cost per read significantly. The aim of this proposal is the development of novel protecting groups with two distinct properties; (a) fluorescence and (b) photolability. That is, the protecting groups would be identified immediately after incorporation of the appropriate nucleotide by laser-induced fluorescence and efficiently removed (>99.9%) upon UV irradiation. To achieve this goal, we propose an exploration of two strategies: syntheses and structural identification of (i) novel fluorescent, 3'-O-photolabile nucleosides, and (ii) novel FRET 3'-Ophotolabile nucleosides bearing an acceptor dye such as fluorescein, rhodarnine, BODIPY, or sulfonated pyrene. Both strategies have the distinct advantage of in situ monitoring of the deprotection step, thus ensuring efficient removal of the protecting group before starting the next BASS cycle. The outcome of this research will provide a basis of a phase II grant for the development of a powerful rapid, high throughput, and low cost DNA sequencing technology. [unreadable] [unreadable]

IC Name
NATIONAL HUMAN GENOME RESEARCH INSTITUTE
  • Activity
    R43
  • Administering IC
    HG
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    148397
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    172
  • Ed Inst. Type
  • Funding ICs
    NHGRI:148397\
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    LASERGEN
  • Organization Department
  • Organization DUNS
    106700375
  • Organization City
    HOUSTON
  • Organization State
    TX
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    77054
  • Organization District
    UNITED STATES