Multiplexed Measurements of Protein Dynamics and Interactions at Extreme Resoluti

Information

  • Research Project
  • 7852460
  • ApplicationId
    7852460
  • Core Project Number
    DP2OD006673
  • Full Project Number
    1DP2OD006673-01
  • Serial Number
    6673
  • FOA Number
    RFA-RM-09-003
  • Sub Project Id
  • Project Start Date
    9/30/2009 - 15 years ago
  • Project End Date
    6/30/2014 - 10 years ago
  • Program Officer Name
    BASAVAPPA, RAVI
  • Budget Start Date
    9/30/2009 - 15 years ago
  • Budget End Date
    6/30/2014 - 10 years ago
  • Fiscal Year
    2009
  • Support Year
    1
  • Suffix
  • Award Notice Date
    9/28/2009 - 15 years ago

Multiplexed Measurements of Protein Dynamics and Interactions at Extreme Resoluti

DESCRIPTION (Provided by the applicant) Abstract: My goal is to develop state-of-art imaging technology that can measure protein complex formation and protein networks in a multiplexed fashion with spatial resolution beyond that of the optical microscopy. At present, a major limitation to clarifying the dynamics of a particular signaling cascade is the inability to visualize multiple (>4) proteins and their interactions simultaneously in real time in the living cell. This is due in part to the interference of spectrally similar species (including cellular autofluorescence) and the mismatch between the spatial resolution of the confocal microscope and the scale of protein interactions. Computational and experimental approaches can help to elucidate many of these interactions, but not all. Specialized microscopy methods have been developed to address some aspects of the problem, but to date, no technology has demonstrated true multiplexed (simultaneous, not sequential) detection of >4 proteins and their complex formation in living cells at spatial resolutions >100 nm. This type of detection is critical for unraveling protein interaction network details, and my proposed work will address that. Specifically, I will: 1) implement novel emission-scanning hyperspectral confocal microscopy hardware to collect information from large numbers of fluorescent species simultaneously at spatial resolution beyond that of the optical microscope. 2) develop corresponding algorithms to spectrally unmix the 6D (X, Y, Z, excitation ?, emission ?, and time) images and provide accurate measurements of fluorophore concentrations even in the presence of energy transfer. This creative approach alleviates limitations of existing multicolor technology by extending my expertise in livecell hyperspectral imaging technology into the "super-resolution" realm. Its success will be enabled by robust multivariate image analysis algorithms. This advance will have far-reaching impact in exploring signaling pathways and networks in biology and biomedicine. Public Health Relevance: The complex symphony of signaling networks still remains a mystery. This project will develop a novel technology to unravel the details of signaling protein networks and pathways with extreme accuracy and spatial resolution. This work is very relevant to Public Health because cell signaling cascades control and regulate response to disease or therapeutic countermeasures.

IC Name
OFFICE OF THE DIRECTOR, NATIONAL INSTITUTES OF HEALTH
  • Activity
    DP2
  • Administering IC
    OD
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    2139978
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    310
  • Ed Inst. Type
  • Funding ICs
    OD:2139978\
  • Funding Mechanism
    Research Projects
  • Study Section
    ZGM1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    SANDIA CORP-SANDIA NATIONAL LABORATORIES
  • Organization Department
  • Organization DUNS
    007113228
  • Organization City
    ALBUQUERQUE
  • Organization State
    NM
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    87123
  • Organization District
    UNITED STATES