Image-based cell sorting using a high throughput fluorescence imaging flow cytometer

Information

  • Research Project
  • 9141581
  • ApplicationId
    9141581
  • Core Project Number
    R43GM119911
  • Full Project Number
    1R43GM119911-01
  • Serial Number
    119911
  • FOA Number
    PA-13-140
  • Sub Project Id
  • Project Start Date
    8/1/2016 - 10 years ago
  • Project End Date
    7/31/2017 - 9 years ago
  • Program Officer Name
    SHEELEY, DOUGLAS
  • Budget Start Date
    8/1/2016 - 10 years ago
  • Budget End Date
    7/31/2017 - 9 years ago
  • Fiscal Year
    2016
  • Support Year
    01
  • Suffix
  • Award Notice Date
    7/26/2016 - 10 years ago
Organizations

Image-based cell sorting using a high throughput fluorescence imaging flow cytometer

? DESCRIPTION (provided by applicant): The ability to isolate subpopulations or even single cells from heterogeneous populations is a fundamental necessity in modern biology and biomedicine. Conventional techniques for separating subpopulations include fluorescence activated cell sorting (FACS), magnetic activated cell sorting (MACS), laser capture microdissection, and DEP array sorting. While all of these techniques are utilized in individual applications, each has its own set of advantages and drawbacks. The technique most widely used for isolating single cells from populations with high purity is FACS, thanks to its relatively gentle sorting mechanism, high sensitivity, multiparameter measurement capability, and ability to analyze both intracellular and surface markers. While FACS is widely used across all areas of cell biology, it has a significant limitation of making sort decisions based only on the average value of a cell's parameters, due to its lack of sub-cellular resolution. For example, FACS only measures the total fluorescence from a cell, and is unable to distinguish where the fluorescent probe is localized within the cell (e.g. on the cell membrane, in the cytoplasm, or in the nucleus) This is a significant limitation if one desires to separate populations of cells that may have translocated a protein from the cytoplasm to the nucleus, or if one wishes to separate cells based on a measurement of the nuclear to cytoplasmic area ratio, for example. Here, we propose to develop an image-based cell sorter based on novel signal processing algorithms and a high throughput imaging flow cytometer, already developed by Omega Biosystems. This tool, to be completed and ready for commercialization by the end of Phase II of this program, will provide a transformative advance in the sensitivity, specificity and spatial resolution of flow sorters for separating single cells and subpopulations from a heterogeneous cellular population. The advent of such a high-resolution cell sorting tool will have a broad impact across biomedicine and cell biology, as well as enable immediate advances in the fields of drug discovery and rare cell detection.

IC Name
NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
  • Activity
    R43
  • Administering IC
    GM
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    225000
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    859
  • Ed Inst. Type
  • Funding ICs
    NIGMS:225000\
  • Funding Mechanism
    SBIR-STTR RPGs
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    OMEGA BIOSYSTEMS, INC.
  • Organization Department
  • Organization DUNS
    079309785
  • Organization City
    LOS ANGELES
  • Organization State
    CA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    900644514
  • Organization District
    UNITED STATES