Drug Design Relating Amebicides to Inhibition of Protein Synthesis.

Abstract

A study of the effect of emetine on protein synthesis in E. histolytica was made on log phase amebas as compared to stationary phase amebas. Sensitivity to emetine was maintained independently of the rate of protein synthesis. Furthermore, both stages of amebas had the same capacity to bind emetine labeled with tritium to ribosomes. The binding of H3 -emetine was not affected by the presence of certain drugs that interfere with energy metabolism, protein synthesis and/or ribosomal function, e.g., dinitrophenol, puromycin, shloroquine and acriflavin. In 'chase' experiments it was shown that the stability of the emetine-ribosome binding is due in part to a hydrogen bonding reaction of the C1 atom of the emetine molecule with the chain elongation site. Finally, evidence was obtained that the capacity to bind emetine provides a basis for conferring drug resistance in amebas. A direct correspondence was found between the degree of drug resistance and the number of binding sites for emetine.

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Document Details

Document Type
Technical Report
Publication Date
Sep 01, 1977
Accession Number
ADA046924

Entities

People

  • Nathan Entner

Organizations

  • New York University

Tags

DTIC Thesaurus Topics

  • Amino Acids
  • Biomedical Research
  • Covalent Bonds
  • Drug Resistance
  • Geiger Counters
  • High Energy
  • Hydrogen Bonds
  • Incubation
  • Inhibition
  • Literature Surveys
  • Materials
  • New York
  • Organelles
  • Resistance
  • Schools
  • Sensitivity
  • Stationary

Fields of Study

  • Biology
  • Chemistry

Readers

  • Cellular and Molecular Pathways of Apoptosis.
  • Infectious Disease/Epidemiology
  • Molecular Genetics