Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
6136050 | Microbes and Infection | 2010 | 7 Pages |
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: 1.34Â 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.
Keywords
PBSLD50CDRs3-DMBPscFvPDBRBDNeutralizing antibodyEnzyme-linked immunosorbent assayELISAEquilibrium constantReceptor binding domainReceptor binding sitesThree dimensionssingle-chain variable fragmentPhosphate-buffered salinevariable region of heavy chainBotulinum neurotoxinsProtein Databasemaltose binding protein
Related Topics
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Immunology
Authors
Hui Wang, Tao Li, Jing Shi, Kun Cai, Xiaojun Hou, Qin Wang, Le Xiao, Wei Tu, Hao Liu, Xiang Gao,