In vitro Reconstitution of Protein Translation of Thermus Thermophilus for Direct

Information

  • Research Project
  • 7609535
  • ApplicationId
    7609535
  • Core Project Number
    R43GM086930
  • Full Project Number
    1R43GM086930-01
  • Serial Number
    86930
  • FOA Number
    PA-08-050
  • Sub Project Id
  • Project Start Date
    2/1/2009 - 15 years ago
  • Project End Date
    1/31/2010 - 14 years ago
  • Program Officer Name
    PORTNOY, MATTHEW
  • Budget Start Date
    2/1/2009 - 15 years ago
  • Budget End Date
    1/31/2010 - 14 years ago
  • Fiscal Year
    2009
  • Support Year
    1
  • Suffix
  • Award Notice Date
    1/26/2009 - 15 years ago

In vitro Reconstitution of Protein Translation of Thermus Thermophilus for Direct

DESCRIPTION (provided by applicant): Directed protein evolution is a powerful technology for generating proteins with desired properties, such as thermostability. There is currently no effective in vitro method to select proteins with enhanced thermostability. Thermostable proteins have a wide range of industrial and medical applications. The aim of this project is to construct a reconstituted in vitro protein synthesis system (thermoPURE system) using purified components from Thermus thermophilus, a bacterium that grows at an optimal temperature of 72oC. The thermoPURE system may allow protein synthesis to be conducted in vitro at elevated temperatures, and due to its low background activities, facilitate in vitro screening and selection or other applications that require elevated temperatures. In conjunction with powerful in vitro selection technologies such as in vitro compartmentalization and ribosome display, the thermoPURE may become the only system that allows in vitro directed evolution of thermostable proteins from their mesophilic origins. During the initial phase of the project, we will clone a complete set of genes for the translation factors, aminoacyl-tRNA synthetases and energy regeneration enzymes from Thermus thermophilus. All proteins will be overexpressed and purified from E. coli. The ribosomes and tRNAs will be purified from a growing culture of Thermus thermophilus. Using our experience and capacity of manufacturing the E. coli version of the reconstituted protein synthesis system (the PURE system), we will reconstitute the protein translation machinery of Thermus thermophilus and demonstrate in vitro protein synthesis at elevated temperatures. In the second phase, we will apply the thermoPURE system for in vitro evolution of mesophilic proteins such as restriction enzymes, RNA polymerases, and single-chain antibodies with an ultimate goal to generate valuable proteins with enhanced thermostability for industrial and medical usage. PUBLIC HEALTH RELEVANCE: Proteins that are stable at elevated temperatures have a wide range of industrial and medical applications. There is currently no effective in vitro method to select proteins with enhanced thermostability. The goal of this project is to provide such a method by constructing a reconstituted in vitro protein synthesis system from purified components of Thermus thermophilus, a bacterium that grows at an optimal temperature of 72oC.

IC Name
NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
  • Activity
    R43
  • Administering IC
    GM
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    233095
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    859
  • Ed Inst. Type
  • Funding ICs
    NIGMS:233095\
  • Funding Mechanism
    SBIR-STTR
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    NEW ENGLAND BIOLABS, INC.
  • Organization Department
  • Organization DUNS
    066605403
  • Organization City
    IPSWICH
  • Organization State
    MA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    019382723
  • Organization District
    UNITED STATES