Ink-Jet System for Protein Crystallization

Information

  • Research Project
  • 6933254
  • ApplicationId
    6933254
  • Core Project Number
    R43CA105883
  • Full Project Number
    1R43CA105883-01A2
  • Serial Number
    105883
  • FOA Number
    PA-02-08
  • Sub Project Id
  • Project Start Date
    7/1/2005 - 19 years ago
  • Project End Date
    12/31/2005 - 18 years ago
  • Program Officer Name
    HEATH, ANNE K
  • Budget Start Date
    7/1/2005 - 19 years ago
  • Budget End Date
    12/31/2005 - 18 years ago
  • Fiscal Year
    2005
  • Support Year
    1
  • Suffix
    A2
  • Award Notice Date
    6/22/2005 - 19 years ago

Ink-Jet System for Protein Crystallization

[unreadable] DESCRIPTION (provided by applicant): In this project, MicroFab will develop a high throughput ink-jet based system to screen for the initial signs of crystallization of membrane proteins, while maximizing the conservation of limited protein samples. Investigators can then repeat successful crystallization experiments determined from the initial screens to grow larger well-ordered crystals for diffraction experiments. The structure of membrane proteins obtained by x-ray crystallography can provide information for computational and structure based drug development. Unfortunately, the crystallization of integral membrane proteins often fails to yield crystals useful for diffraction analysis. Membrane protein (MP) crystallization difficulties can be attributed to their very narrow metastable solubility regions and scarcity of material. The consensus solution to these problems is to decrease protein consumption and narrow the sampling of crystal growth conditions by using smaller screening volumes. Ink-jet dispensing is a technology capable of reliably delivering small volumes ranging from picoliter to microliter, the later through accretion. In Phase I MicroFab will determine the operational parameters required to dispense protein and detergent screening solutions using ink-jet devices. MicroFab will also determine the optimum process for coalescing and mixing of these solutions under oil. Finally, MicroFab will conduct initial crystallization condition screens of membrane proteins using ink-jet dispensing. We expect these experiments to provide critical information that will ultimately enable high throughput picoliter MP crystal growth assays as a mainstream technique. [unreadable] [unreadable]

IC Name
NATIONAL CANCER INSTITUTE
  • Activity
    R43
  • Administering IC
    CA
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    108500
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    396
  • Ed Inst. Type
  • Funding ICs
    NCI:108500\
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    MICROFAB TECHNOLOGIES, INC.
  • Organization Department
  • Organization DUNS
  • Organization City
    PLANO
  • Organization State
    TX
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    75074
  • Organization District
    UNITED STATES