| Literature DB >> 36006520 |
Jorge Ramirez-Franco1, Fodil Azzaz1, Marion Sangiardi1, Géraldine Ferracci2, Fahamoe Youssouf1, Michel Robert Popoff3, Michael Seagar1, Christian Lévêque4, Jacques Fantini1, Oussama El Far5.
Abstract
Botulinum neurotoxin serotype B (BoNT/B) uses two separate protein and polysialoglycolipid-binding pockets to interact with synaptotagmin 1/2 and gangliosides. However, an integrated model of BoNT/B bound to its neuronal receptors in a native membrane topology is still lacking. Using a panel of in silico and experimental approaches, we present here a new model for BoNT/B binding to neuronal membranes, in which the toxin binds to a preassembled synaptotagmin-ganglioside GT1b complex and a free ganglioside allowing a lipid-binding loop of BoNT/B to interact with the glycone part of the synaptotagmin-associated GT1b. Furthermore, our data provide molecular support for the decrease in BoNT/B sensitivity in Felidae that harbor the natural variant synaptotagmin2-N59Q. These results reveal multiple interactions of BoNT/B with gangliosides and support a novel paradigm in which a toxin recognizes a protein/ganglioside complex.Entities:
Keywords: Botulinum neurotoxin type B; Gangliosides; Molecular modelling; Synaptotagmin
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Year: 2022 PMID: 36006520 DOI: 10.1007/s00018-022-04527-4
Source DB: PubMed Journal: Cell Mol Life Sci ISSN: 1420-682X Impact factor: 9.207