Botulinum neurotoxin type C cleaves a single Lys-Ala bond within the carboxyl-terminal region of syntaxins

J Biol Chem. 1995 May 5;270(18):10566-70. doi: 10.1074/jbc.270.18.10566.

Abstract

Botulinum neurotoxin serotype C (BoNT/C) is a 150-kDa protein produced by Clostridium botulinum, which causes animal botulism. In contrast to the other botulinum neurotoxins that contain one atom of zinc, highly purified preparations of BoNT/C bind two atoms of zinc per toxin molecule. BoNT/C is a zinc-endopeptidase that cleaves syntaxin 1A at the Lys253-Ala254 and syntaxin 1B at the Lys252-Ala253 peptide bonds, only when they are inserted into a lipid bilayer. The other Lys-Ala bond present within the carboxyl-terminal region is not hydrolyzed. Syntaxin isoforms 2 and 3 are also cleaved by BoNT/C, while syntaxin 4 is resistant. These data suggest that BoNT/C recognizes a specific spatial organization of syntaxin, adopted upon membrane insertion, which brings a selected Lys-Ala peptide bond of its carboxyl-terminal region to the active site of this novel metalloproteinase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alanine
  • Amino Acid Sequence
  • Animals
  • Botulinum Toxins / chemistry
  • Botulinum Toxins / metabolism*
  • In Vitro Techniques
  • Lipid Bilayers
  • Lysine
  • Membrane Proteins / metabolism*
  • Metalloendopeptidases / chemistry
  • Metalloendopeptidases / metabolism*
  • Molecular Sequence Data
  • Nerve Tissue Proteins / metabolism
  • Peptide Fragments / chemistry
  • Qa-SNARE Proteins
  • Rats
  • Synaptosomes / metabolism
  • Syntaxin 1
  • Zinc / chemistry

Substances

  • Lipid Bilayers
  • Membrane Proteins
  • Nerve Tissue Proteins
  • Peptide Fragments
  • Qa-SNARE Proteins
  • Stx1a protein, rat
  • Syntaxin 1
  • Metalloendopeptidases
  • Botulinum Toxins
  • Zinc
  • Lysine
  • Alanine

Grants and funding