Protein-chemical analysis of pertussis toxin reveals homology between the subunits S2 and S3, between S1 and the A chains of enterotoxins of Vibrio cholerae and Escherichia coli and identifies S2 as the haptoglobin-binding subunit

FEBS Lett. 1986 Aug 18;204(2):336-40. doi: 10.1016/0014-5793(86)80839-0.

Abstract

The purified toxin of Bordetella pertussis was dissociated in 5 M urea in the presence of immobilized haptoglobin. The toxin was dissociated in free S1, free S5 and the free complexes S2-S4 and S3-S4, with S2-S4 as the only haptoglobin-binding moiety, identifying S2 as the haptoglobin-binding protein. Partial NH2-terminal amino acid sequences were obtained from the dissimilar toxin subunits, after separation by SDS-polyacrylamide gel electrophoresis followed by electroblotting onto polybrene-coated glass-fiber sheets. The sequences reveal extensive homology of the N-terminal portions of the constitutive subunits S2 and S3 and between S1 and the enterotoxin A chains of Vibrio cholerae and Escherichia coli.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Base Sequence*
  • Carrier Proteins*
  • Chromatography, Affinity
  • Chromatography, Ion Exchange
  • Electrophoresis, Polyacrylamide Gel
  • Enterotoxins*
  • Escherichia coli / metabolism
  • Haptoglobins*
  • Pertussis Toxin*
  • Sequence Homology, Nucleic Acid*
  • Vibrio cholerae / metabolism
  • Virulence Factors, Bordetella*

Substances

  • Carrier Proteins
  • Enterotoxins
  • Haptoglobins
  • Virulence Factors, Bordetella
  • stN protein, Vibrio cholerae
  • Pertussis Toxin