Ganglioside GT1b as a complementary receptor component for Clostridium botulinum neurotoxins

Microb Pathog. 1998 Aug;25(2):91-9. doi: 10.1006/mpat.1998.0214.

Abstract

Clostridium botulinum type B neurotoxin (BoNT/B) recognizes a complex of synaptotagmin II and ganglioside GT1b or GD1a as the high-affinity toxin binding site. Recombinant deletion mutants of synaptotagmin II allowed us to demonstrate that the N-terminal domain including the transmembrane region retains BoNT/B binding activity while the C-terminal domain is not involved in constituting the BoNT/B receptor. BoNT/B binding to reconstituted lipid vesicles containing synaptotagmin II and gangliosides showed that GT1b and GD1a confer the difference in the maximum binding capacity but not in the dissociation constant. The direct binding of GT1b to the deletion mutants revealed that the transmembrane region is required to bind GT1b, suggesting that synaptotagmin II binds to the ceramide portion of gangliosides within the plasma membrane. A monoclonal antibody against GT1b effectively inhibited not only BoNT/B binding to the reconstituted lipid vesicles and brain synaptosomes but also type A BoNT (BoNT/A) binding to brain synaptosomes. In addition, the monoclonal antibody antagonized the action of both BoNT/A and BoNT/B on synaptic transmission of rat superior cervical ganglion neurons. These results suggest that GT1b functions as a component of the receptor complex.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Monoclonal
  • Binding Sites
  • Botulinum Toxins / metabolism*
  • Botulinum Toxins, Type A
  • Brain / microbiology*
  • Carbohydrate Sequence
  • Cell Membrane / microbiology
  • Clostridium botulinum / physiology*
  • Gangliosides / analysis
  • Gangliosides / chemistry
  • Gangliosides / immunology
  • Gangliosides / physiology*
  • Kinetics
  • Molecular Sequence Data
  • Mutagenesis
  • Nerve Tissue Proteins / chemistry
  • Nerve Tissue Proteins / physiology*
  • Rats
  • Recombinant Fusion Proteins / metabolism
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / metabolism
  • Sequence Deletion
  • Synaptosomes / microbiology*
  • Synaptotagmin II

Substances

  • Antibodies, Monoclonal
  • Gangliosides
  • Nerve Tissue Proteins
  • Recombinant Fusion Proteins
  • Recombinant Proteins
  • Synaptotagmin II
  • Syt2 protein, rat
  • rimabotulinumtoxinB
  • trisialoganglioside GT1
  • Botulinum Toxins
  • Botulinum Toxins, Type A