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Structural Analysis of Botulinum Neurotoxin Type G Receptor Binding

Authors :
Rory N. Pruitt
D. Borden Lacy
Darren J. Mushrush
Andrew P.-A. Karalewitz
John Schmitt
Joseph T. Barbieri
Benjamin W. Spiller
Desirée A. Benefield
Source :
Biochemistry. 49:5200-5205
Publication Year :
2010
Publisher :
American Chemical Society (ACS), 2010.

Abstract

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 (Syt)-I and SytII, homologous synaptic vesicle proteins. We observe conditions in which BoNT/B binds both Syt isoforms, but BoNT/G only binds SytI. Both serotypes bind ganglioside GT1b. The BoNT/G receptor-binding domain crystal structure provides a context for examining these binding interactions and a platform to understand the physiological relevance of different Syt receptor isoforms in vivo.

Details

ISSN :
15204995 and 00062960
Volume :
49
Database :
OpenAIRE
Journal :
Biochemistry
Accession number :
edsair.doi.dedup.....2d3e8fe994aa3468f2c547fdd5b84637
Full Text :
https://doi.org/10.1021/bi100412v