Novel Metal Affinity Peptide and Protein Separations

Information

  • Research Project
  • 6336050
  • ApplicationId
    6336050
  • Core Project Number
    R43RR016133
  • Full Project Number
    1R43RR016133-01
  • Serial Number
    16133
  • FOA Number
  • Sub Project Id
  • Project Start Date
    3/15/2001 - 23 years ago
  • Project End Date
    2/14/2002 - 22 years ago
  • Program Officer Name
    SWAIN, AMY L
  • Budget Start Date
    3/15/2001 - 23 years ago
  • Budget End Date
    2/14/2002 - 22 years ago
  • Fiscal Year
    2001
  • Support Year
    1
  • Suffix
  • Award Notice Date
    3/9/2001 - 23 years ago

Novel Metal Affinity Peptide and Protein Separations

DESCRIPTION: (Applicant's abstract) The long-term objective is to use a novel separations technology to improve markedly the efficiency of peptide and protein separations and to extend these separations to a wide variety of peptides and proteins. The specific aim of the Phase I research is to test novel supported ligands for their ability to separate selectively tripeptides (capped and uncapped), each of which is composed of the same amino acid chosen from among those with side groups sulfhydryl (methionine, cysteine), protonated amine (lysine), carboxyl (aspartic acid, glutamic acid), and imidazole (histidine). Success in the Phase I and Phase II studies has the potential to make possible a rapid means for achieving highly selective separations of a wide variety ofpeptides and proteins. The research design involves the use in colunm form of available supported materials consisting of ligands chemically bonded to several supports to separate individual tripeptides from their mixtures with different tripeptides. Separations will be further enhanced by altering pH and eluent conditions. It is expected that separation factors of 10 to 100 will be achieved, making bind-release operations possible in many cases. PROPOSED COMMERCAIL APPLICATION: Successful completion fo the research would open the way in Phase II and beyond to meet two important commercial needs of peptide and protein separations. First, use of a novel separations to be dramatically improved through a reduced number of process steps, higher selectivities, and stronger binding. Second, selective recognition of protonated amie and carboxyl groups would greatly expand the number of peptides and proteins that could be effectively separated.

IC Name
NATIONAL CENTER FOR RESEARCH RESOURCES
  • Activity
    R43
  • Administering IC
    RR
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    89984
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    371
  • Ed Inst. Type
  • Funding ICs
    NCRR:89984\
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    IBC ADVANCED TECHNOLOGIES, INC.
  • Organization Department
  • Organization DUNS
  • Organization City
    AMERICAN FORK
  • Organization State
    UT
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    84003
  • Organization District
    UNITED STATES