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Molecular landscape of BoNT/B bound to a membrane-inserted synaptotagmin/ganglioside complex.
Ramirez-Franco, Jorge; Azzaz, Fodil; Sangiardi, Marion; Ferracci, Géraldine; Youssouf, Fahamoe; Popoff, Michel Robert; Seagar, Michael; Lévêque, Christian; Fantini, Jacques; El Far, Oussama.
Afiliação
  • Ramirez-Franco J; 1INSERM, Aix-Marseille Université (AMU), UMR 1072, Unité de Neurobiologie des canaux Ioniques et de la Synapse, 13015, Marseille, France.
  • Azzaz F; 1INSERM, Aix-Marseille Université (AMU), UMR 1072, Unité de Neurobiologie des canaux Ioniques et de la Synapse, 13015, Marseille, France.
  • Sangiardi M; 1INSERM, Aix-Marseille Université (AMU), UMR 1072, Unité de Neurobiologie des canaux Ioniques et de la Synapse, 13015, Marseille, France.
  • Ferracci G; Aix-Marseille Université (AMU), CNRS, INP, Institute of Neurophysiopathology, UMR7051, PINT, PFNT, Marseille, France.
  • Youssouf F; 1INSERM, Aix-Marseille Université (AMU), UMR 1072, Unité de Neurobiologie des canaux Ioniques et de la Synapse, 13015, Marseille, France.
  • Popoff MR; Institut Pasteur, Unité des Toxines Bactériennes, UMR CNRS 2001, Paris, France.
  • Seagar M; 1INSERM, Aix-Marseille Université (AMU), UMR 1072, Unité de Neurobiologie des canaux Ioniques et de la Synapse, 13015, Marseille, France.
  • Lévêque C; 1INSERM, Aix-Marseille Université (AMU), UMR 1072, Unité de Neurobiologie des canaux Ioniques et de la Synapse, 13015, Marseille, France. christian.leveque@univ-amu.fr.
  • Fantini J; 1INSERM, Aix-Marseille Université (AMU), UMR 1072, Unité de Neurobiologie des canaux Ioniques et de la Synapse, 13015, Marseille, France.
  • El Far O; 1INSERM, Aix-Marseille Université (AMU), UMR 1072, Unité de Neurobiologie des canaux Ioniques et de la Synapse, 13015, Marseille, France. oussama.el-far@inserm.fr.
Cell Mol Life Sci ; 79(9): 496, 2022 Aug 25.
Article em En | MEDLINE | ID: mdl-36006520
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sinaptotagmina II / Gangliosídeos Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sinaptotagmina II / Gangliosídeos Idioma: En Ano de publicação: 2022 Tipo de documento: Article