Novel Breast Cancer Therapeutics Based on Bacterial Cupredoxin

Abstract

The tumor suppressor p53 is a major player in cell growth, genomic stability and cell death. Recent in vivo work suggested that bacterial Pseudomonas aeruginosa azurin can enter cancer cells and interact with p53 promoting cell death. Despite being a novel concept to target cancer, there are no thermodynamic details known for the proposed azurin-p53 complex. This project aims to fill this gap by employing biophysical methods in conjunction with purified proteins in vitro to address four aims. We will reveal (1) which p53 domain interacts with azurin, (2) the molecular mechanism by which azurin increases cellular levels of p53, (3) the region on azurin that interacts with p53 and (4) use the acquired information to propose smaller molecules that retain properties of azurin. We have found that azurin binds to the unstructured N-terminal domain of p53 and a small peptide is able to reproduce part of the azurin interaction. We have also assessed how Cu is metabolized inside cells as well has how the crowdedness of the cell milieu affects proteins. We have made several key discoveries that will aid in the development of azurin-based molecules that can be used as new treatments of cancer.

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Document Details

Document Type
Technical Report
Publication Date
Sep 01, 2008
Accession Number
ADA487517

Entities

People

  • Pernilla Wittung-Stafshede

Organizations

  • Rice University

Tags

DTIC Thesaurus Topics

  • Amines
  • Bacterial Proteins
  • Biomedical And Dental Materials
  • Carrier Proteins
  • Cell Physiological Processes
  • Chemical Reactions
  • Chemical Stability
  • Chemical Synthesis
  • Chemistry
  • Computational Biology
  • Crystal Structure
  • Free Radicals
  • Molecular Dynamics
  • Polymer Chemistry
  • Polymeric Films
  • Proteomics

Fields of Study

  • Chemistry

Readers

  • Immunology and Pathology
  • Neurological Diseases/Conditions/Disorders
  • Oncology (Cancer Research).

Technology Areas

  • Biotechnology