4.4 Article

Structural Analysis of Botulinum Neurotoxin Type G Receptor Binding

Journal

BIOCHEMISTRY
Volume 49, Issue 25, Pages 5200-5205

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/bi100412v

Keywords

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Funding

  1. NIAID NIH HHS [R01 AI075259, AI075259, U54 AI057153-075849, 2-U54-AI-057153, R01 AI075259-04, U54 AI057153] Funding Source: Medline
  2. NIGMS NIH HHS [T32 GM008320] Funding Source: Medline

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Botulinum neurotoxin (BoNT) binds peripheral neurons at the neuromuscular junction through a dual-receptor mechanism that includes interactions with ganglioside and protein receptors. The receptor identities vary depending on BoNT serotype (A-G). BoNT/B and BoNT/G bind the luminal domains of synaptotagmin I and II, homologous synaptic vesicle proteins. We observe conditions under which BoNT/B binds both Syt isoforms, but BoNT/G binds only Sytl. Both serotypes bind ganglioside G(T1b). The BoNT/G receptor-binding domain crystal structure provides a context for examining these binding interactions and a platform for understanding the physiological relevance of different Syt receptor isoforms in vivo.

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