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Updated: May 2, 2026

A High-throughput-compatible FRET-based Platform for Identification and Characterization of Botulinum Neurotoxin Light Chain Modulators
Published on: December 27, 2013
Identification of the synaptic vesicle glycoprotein 2 receptor binding site in botulinum neurotoxin A
Jasmin Strotmeier1, Stefan Mahrhold2, Nadja Krez1
1Institut für Toxikologie, OE 5340, Medizinische Hochschule Hannover, 30623 Hannover, Germany.
Abstract:
Botulinum neurotoxins (BoNTs) inhibit neurotransmitter release by hydrolysing SNARE proteins. The most important serotype BoNT/A employs the synaptic vesicle glycoprotein 2 (SV2) isoforms A-C as neuronal receptors. Here, we identified their binding site by blocking SV2 interaction using monoclonal antibodies with characterised epitopes within the cell binding domain (HC). The site is located on the backside of the conserved ganglioside binding pocket at the interface of the HCC and HCN subdomains. The dimension of the binding pocket was characterised in detail by site directed mutagenesis allowing the development of potent inhibitors as well as modifying receptor binding properties.
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