4.4 Article

Identification of a Unique Ganglioside Binding Loop within Botulinum Neurotoxins C and D-SA

Journal

BIOCHEMISTRY
Volume 49, Issue 37, Pages 8117-8126

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/bi100865f

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Funding

  1. National Institutes of Health Regional Center of Excellence for Biodefense and Emerging Infectious Diseases Research Program
  2. Great Lakes Regional Center of Excellence [1-U54-AI-057153]
  3. National Institute of Neurological Disorders and Stroke [NS061763]

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The botulinum neurotoxins (BoNTs) are the most potent protein toxins for humans. There are seven serotypes of BoNTs (A-G) based on a lack of cross antiserum neutralization. BoNTs utilize gangliosides as components of the host receptors for binding and entry into neurons. Members of BoNT/C and BoNT/D serotypes include mosaic toxins that are organized in D/C and C/D toxins. One D/C mosaic toxin, BoNT/D-South Africa (BoNT/D-SA), was not fully neutralized by immunization with BoNT serotype C or D, which stimulated this study. Here the crystal structures of the receptor binding domains of BoNT/C, BoNT/D, and BoNT/D-SA are presented. Biochemical and cell binding studies show that BoNT/C and BoNT/D-SA possess unique mechanisms for ganglioside binding. These studies provide new information about how the BoNTs can enter host cells as well as a basis for understanding the immunological diversity of these neurotoxins.

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