The synaptic vesicle protein 2C mediates the uptake of botulinum neurotoxin A into phrenic nerves

被引:249
作者
Mahrhold, S
Rummel, A
Bigalke, H
Davletov, B
Binz, T
机构
[1] Hannover Med Sch, Inst Biochem, D-30623 Hannover, Germany
[2] Hannover Med Sch, Inst Toxicol, D-30623 Hannover, Germany
[3] MRC, Mol Biol Lab, Cambridge CB2 2QH, England
来源
FEBS LETTERS | 2006年 / 580卷 / 08期
基金
英国医学研究理事会;
关键词
botulinum neurotoxin; ganglioside; phrenic nerve; protein receptor; SV2;
D O I
10.1016/j.febslet.2006.02.074
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Botulinum neurotoxins (BoNTs) inhibit neurotransmitter release by selectively cleaving core components of the vesicular fusion machinery. The synaptic vesicle proteins Synaptotagmin-I and -II act as receptors for BoNT/B and BoNT/G. Here we show that BoNT/A also interacts with a synaptic vesicle protein, the synaptic vesicle glycoprotein 2C (SV2C), but not with the homologous proteins SV2A and SV2B. Binding of BoNT/A occurs at the membrane juxtaposed region preceding transmembrane domain 8. A peptide comprising the intravesicular domain between transmembrane domains 7 and 8 specifically reduces the neurotoxicity of BoNT/A at phrenic nerve preparations demonstrating the physiological relevance of this interaction. (c) 2006 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:2011 / 2014
页数:4
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