Fluorescent Chemosensors for Carbohydrates

Information

  • Research Project
  • 6775243
  • ApplicationId
    6775243
  • Core Project Number
    R15GM057855
  • Full Project Number
    3R15GM057855-02S1
  • Serial Number
    57855
  • FOA Number
    PA-99-62
  • Sub Project Id
  • Project Start Date
    9/1/1998 - 26 years ago
  • Project End Date
    3/31/2006 - 18 years ago
  • Program Officer Name
    MARINO, PAMELA
  • Budget Start Date
    9/1/2002 - 22 years ago
  • Budget End Date
    3/31/2006 - 18 years ago
  • Fiscal Year
    2003
  • Support Year
    2
  • Suffix
    S1
  • Award Notice Date
    7/17/2003 - 21 years ago

Fluorescent Chemosensors for Carbohydrates

DESCRIPTION: (provided by applicant) Because of their potential for nondestructive detection and cell permeability, fluorescent chemosensors for carbohydrates can play a critical role in glycobiology. The objectives of this continuing research program involve the application of molecular clefts as fluorogenic sensors suitable for biological studies of monosaccharides and carbohydrate derivatives. The scope of these investigations build on previous results in which novel signal transduction mechanisms were identified and shown to proceed by substituent changes of the fluorophore component. In an effort to significantly augment the fluorescence signal intensity over conventional Photoinduced Electron Transfer (PET) fluorescence as well as red-shift this response to longer wavelength emission, new sensors are proposed which utilize Resonance Energy Transfer fluorescence (FRET). This research plan begins by investigating intermolecular energy transfer between two donor/acceptor Forster-pairs. Given the calculated distance of separation (14 Angstroms) for one saccharide complexed between two receptor components, well known donor/acceptor dyes that coincide with this Forster distance such as diethylaminocoumarin and fluorescein are incorporated into the sensor design. Subsequent plans utilize rigid aromatic diimide chromophores as non-fluorescent molecular scaffolds to which recognition groups are appended via benzyl-imide bonds. Cooperative binding of analyte between receptor sites is expected to decrease torsional motion and enhance energy transfer rates between coupled FRET cassettes. In addition to investigating simple monosaccharides via FRET based sensors, carbohydrate derivatives relevant to glucose metabolism and cell membrane carbohydrates are also targeted for fluorimetric detection. Specifically, glucose-6-phosphate and N-acetylneuraminic acid via 2-point bifunctional binding sites from phenylboronic acid and guanidinium receptors. Second messenger myo-Inositol-triphosphate via bis- guanidinium groups and glucosamine sensing through crown-ether coordination are also included in these fluorometry studies.

IC Name
NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
  • Activity
    R15
  • Administering IC
    GM
  • Application Type
    3
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    30098
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    859
  • Ed Inst. Type
    SCHOOLS OF ARTS AND SCIENCES
  • Funding ICs
    NIGMS:30098\
  • Funding Mechanism
  • Study Section
    MCHA
  • Study Section Name
    Medicinal Chemistry Study Section
  • Organization Name
    NEW MEXICO INST OF MINING &TECHNOLOGY
  • Organization Department
    CHEMISTRY
  • Organization DUNS
    041358904
  • Organization City
    SOCORRO
  • Organization State
    NM
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    87801
  • Organization District
    UNITED STATES