Neutralization of HIV by bifunctional proteins

Information

  • Research Project
  • 6404776
  • ApplicationId
    6404776
  • Core Project Number
    R43AI048267
  • Full Project Number
    1R43AI048267-01A1
  • Serial Number
    48267
  • FOA Number
  • Sub Project Id
  • Project Start Date
    7/15/2001 - 23 years ago
  • Project End Date
    1/15/2002 - 23 years ago
  • Program Officer Name
    RYAN, KEVIN W.
  • Budget Start Date
    7/15/2001 - 23 years ago
  • Budget End Date
    1/15/2002 - 23 years ago
  • Fiscal Year
    2001
  • Support Year
    1
  • Suffix
    A1
  • Award Notice Date
    7/13/2001 - 23 years ago
Organizations

Neutralization of HIV by bifunctional proteins

DESCRIPTION (Provided by the applicant): Osel was founded to develop and commercialize a novel approach to prevent vaginal HIV transmission in women. We propose to create bifunctional proteins containing an HIV-binding domain (CD4) and a lactobacillus-binding domain. Such bifunctional proteins will multivalently crosslink HIV to the lactobacilli abundantly resident on the mucosal microflora, thus preventing immobilized viral particles from progressing to infect underlying host cells. Bound viruses may be inactivated by either hydrogen peroxide produced by lactobacilli or removed from the body by normal sloughing of mucosal bacteria. Thus, application of such bifunctional proteins onto the vaginal mucosa up to 24 hours before vaginal intercourse should significantly reduce the number of available HIV particles introduced by semen, thereby reducing or eliminating the risk of viral transmission. This novel approach would create a novel barrier to viral transmission that is different from traditional approaches. Therefore, it should act synergistically with vaccines, condoms, or other potential methods of protection. The underlying concept is generally applicable to other viruses that infect at other anatomical sites, such as respiratory or intestinal mucosa. The work being proposed include (i) selection of lactobacilli-specific binding peptides (LSP) via combinatorial phage display libraries followed by their genetic transfer to the soluble CD4 protein to create bifunctional CD4-LSP proteins, and (ii) testing the ability of such bifunctional proteins to neutralize HIV in vitro in the presence of lactobacilli. PROPOSED COMMERCIAL APPLICATION: NOT AVAILABLE

IC Name
NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES
  • Activity
    R43
  • Administering IC
    AI
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    139650
  • Sub Project Total Cost
  • ARRA Funded
  • CFDA Code
    856
  • Ed Inst. Type
  • Funding ICs
    NIAID:139650\
  • Funding Mechanism
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    OSEL, INC.
  • Organization Department
  • Organization DUNS
    001910777
  • Organization City
    SANTA CLARA
  • Organization State
    CA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    95054
  • Organization District
    UNITED STATES