Literature DB >> 20650331

A new neutralizing antibody against botulinum neurotoxin B recognizes the protein receptor binding sites for synaptotagmins II.

Hui Wang1, Tao Li, Jing Shi, Kun Cai, Xiaojun Hou, Qin Wang, Le Xiao, Wei Tu, Hao Liu, Xiang Gao.   

Abstract

Botulinum neurotoxins (BoNts) pose a biological hazard to humans and a serious potential bioweapon threat. Given the safety concern regarding the currently used equine antitoxin therapy for botulism, it is imperative to develop agents that are effective binding inhibitors. The aim of this study was to identify a novel neutralizing antibody against botulinum neurotoxin B (BoNtb) that recognizes the protein receptor binding sites for synaptotagmins II. This antibody showed significant dose-dependent protection against lethal toxin challenge in vivo at an intraperitoneal (i.p.) dose 10 times the half lethal dose (LD50). We proved that the efficacy of SC12 was based on its counteraction on the recognition and binding of BoNtb to target cells, resulting from the combination of antibody with the high affinity (KD: 1.34 nM) to protein receptor binding sites of BoNt by targeting a 25-mer dominant antigenic site on Hcc region (residues 1253-1277). The structure of the site targeted by this antibody overlaps the pocket-like protein receptor binding sites located at the distal tip of toxin molecule. Information gained from this study will facilitate the development of potent inhibitors that prevent the binding of BoNts with its receptors.
Copyright © 2010 Institut Pasteur. Published by Elsevier SAS. All rights reserved.

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Year:  2010        PMID: 20650331     DOI: 10.1016/j.micinf.2010.07.002

Source DB:  PubMed          Journal:  Microbes Infect        ISSN: 1286-4579            Impact factor:   2.700


  1 in total

1.  Potent neutralization of botulinum neurotoxin/B by synergistic action of antibodies recognizing protein and ganglioside receptor binding domain.

Authors:  Changchun Chen; Shuhui Wang; Huajing Wang; Xiaoyan Mao; Tiancheng Zhang; Guanghui Ji; Xin Shi; Tian Xia; Weijia Lu; Dapeng Zhang; Jianxin Dai; Yajun Guo
Journal:  PLoS One       Date:  2012-08-29       Impact factor: 3.240

  1 in total

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