Biological Activities of the Peptides of Staphylococcal Enterotoxin C Formed by Limited Tryptic Hydrolysis.

Abstract

Staphylococcal entertoxin C1 is converted to a doubly cleaved molecule by trypsin digestion with one of the scissions internal to the disulfide loop and one external to it. The larger, disulfide-containing polypeptide (Mr = 22,000) exhibited excellent binding to antiserum to the intact enterotoxin. The residual amino terminal fragment (Mr = 6,500) also bound to this antibody but only weakly. Only the carboxyl terminal carboxamidomethylated moiety of the 22,000 Mr polypeptide (Mr = 19,000) combined with anti-enterotoxin C1. Both the 22,000 Mr and 6,500 Mr polypeptides could partially inhibit the binding of entertoxin C1 to its antibody in a competitive system. It is suggested that enterotoxin C1 possesses three major antigenic determinants, two on Cam 19,000 and one on the 6,500 Mr fragment.

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Document Details

Document Type
Technical Report
Publication Date
May 08, 1978
Accession Number
ADA054653

Entities

People

  • Beverly A. Morlock
  • Leonard Spero

Organizations

  • United States Army Medical Research Institute of Infectious Diseases

Tags

Communities of Interest

  • Biomedical

DTIC Thesaurus Topics

  • Albumins
  • Amino Acids
  • Antibodies
  • Biological Toxins
  • Biomedical And Dental Materials
  • Biomedical Research
  • Chemical Synthesis
  • Chemistry
  • Crystal Structure
  • Immune Serums
  • Infectious Diseases
  • Laboratory Animals
  • Materials
  • Molecular Weight
  • Molecules
  • Physical Properties
  • Proteins

Fields of Study

  • Biology

Readers

  • Immunology
  • Medical Imaging.
  • Microbial Pathology