Development of a Novel, Proteinase-Activated Toxin Targeting Tumor Neovascularization

Abstract

The purpose of this research is to target Clostridium septicum alpha toxin to the cells in blood vessels that are undergoing angiogenesis durin there invasion of tumors. This will be accomplished by altering the normal proteolytic activation site of alpha toxin to one which is activated by gelatinase enzymes which are primarily active in this endothelial cells. The presentation of the gelatinase cleavage in alpha toxin appeared to be problematic since we were unable to generate mutants of alpha toxin with the normal furin activation site replaced with a gelatinase A and B that could be efficiently activated with gelatinase B. It was clear that when alpha toxin was largely misfolded and inactive that the engineered gelatinase site could be efficiently cleaved by gelatinase B. Therefore, in the light of this information and new information that we and others have generated with respect to gelatinase activity and the structure-function relationships of alpha toxin we are pursuing several different approaches to solve the gelatinase activation problem of alpha toxin. We have also begun the application of our approach to other cytolytic toxins which may be more amenable to the engineering of gelatinase switches into their structures so that they can be targeted them to blood vessels which are feeding tumors. 14. SUBJECT TERMS 15. NUMBER OF PAGES

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Document Details

Document Type
Technical Report
Publication Date
Oct 01, 1999
Accession Number
ADA386573

Entities

People

  • Rodney K. Tweten

Organizations

  • University of Oklahoma

Tags

DTIC Thesaurus Topics

  • Amino Acids
  • Angiogenesis
  • Blood
  • Blood Vessels
  • Breast Cancer
  • Cells
  • Chemistry
  • Cysteine
  • Endothelial Cells
  • Engineering
  • Laboratory Animals
  • Materials
  • Membranes
  • Molecules
  • Neoplasms
  • Targeting
  • Therapy

Fields of Study

  • Biology
  • Computer science

Readers

  • Microbial Pathology
  • Molecular Biology and Genetics
  • Systems Analysis and Design