Suppr超能文献

鉴定肉毒梭菌神经毒素 C 和 D-SA 内独特的神经节苷脂结合环。

Identification of a unique ganglioside binding loop within botulinum neurotoxins C and D-SA .

机构信息

Department of Microbiology and of Molecular Genetics, Medical College of Wisconsin,Milwaukee, Wisconsin 53226-3548, USA.

出版信息

Biochemistry. 2010 Sep 21;49(37):8117-26. doi: 10.1021/bi100865f.

Abstract

The botulinum neurotoxins (BoNTs) are the most potent protein toxins for humans. There are seven serotypes of BoNTs (A-G) based on a lack of cross antiserum neutralization. BoNTs utilize gangliosides as components of the host receptors for binding and entry into neurons. Members of BoNT/C and BoNT/D serotypes include mosaic toxins that are organized in D/C and C/D toxins. One D/C mosaic toxin, BoNT/D-South Africa (BoNT/D-SA), was not fully neutralized by immunization with BoNT serotype C or D, which stimulated this study. Here the crystal structures of the receptor binding domains of BoNT/C, BoNT/D, and BoNT/D-SA are presented. Biochemical and cell binding studies show that BoNT/C and BoNT/D-SA possess unique mechanisms for ganglioside binding. These studies provide new information about how the BoNTs can enter host cells as well as a basis for understanding the immunological diversity of these neurotoxins.

摘要

肉毒神经毒素(BoNTs)是对人类最有效的蛋白毒素。根据缺乏交叉抗血清中和作用,BoNTs 分为 7 种血清型(A-G)。BoNTs 将神经节苷脂作为宿主受体的组成部分用于结合和进入神经元。BoNT/C 和 BoNT/D 血清型的成员包括以 D/C 和 C/D 毒素形式存在的嵌合毒素。一种 D/C 嵌合毒素 BoNT/D-南非(BoNT/D-SA),不能完全被 BoNT 血清型 C 或 D 的免疫接种所中和,这激发了本研究。本文展示了 BoNT/C、BoNT/D 和 BoNT/D-SA 的受体结合结构域的晶体结构。生化和细胞结合研究表明,BoNT/C 和 BoNT/D-SA 具有独特的神经节苷脂结合机制。这些研究提供了关于 BoNTs 如何进入宿主细胞的新信息,以及理解这些神经毒素免疫多样性的基础。

相似文献

1
Identification of a unique ganglioside binding loop within botulinum neurotoxins C and D-SA .
Biochemistry. 2010 Sep 21;49(37):8117-26. doi: 10.1021/bi100865f.
2
Unique ganglioside binding by botulinum neurotoxins C and D-SA.
FEBS J. 2011 Dec;278(23):4486-96. doi: 10.1111/j.1742-4658.2011.08166.x. Epub 2011 May 31.
3
Botulinum neurotoxin serotype C associates with dual ganglioside receptors to facilitate cell entry.
J Biol Chem. 2012 Nov 23;287(48):40806-16. doi: 10.1074/jbc.M112.404244. Epub 2012 Oct 1.
4
Novel ganglioside-mediated entry of botulinum neurotoxin serotype D into neurons.
J Biol Chem. 2011 Jul 29;286(30):26828-37. doi: 10.1074/jbc.M111.254086. Epub 2011 Jun 1.
5
Unique biological activity of botulinum D/C mosaic neurotoxin in murine species.
Infect Immun. 2012 Aug;80(8):2886-93. doi: 10.1128/IAI.00302-12. Epub 2012 Jun 4.
9
Exchange of the H(CC) domain mediating double receptor recognition improves the pharmacodynamic properties of botulinum neurotoxin.
FEBS J. 2011 Dec;278(23):4506-15. doi: 10.1111/j.1742-4658.2011.08196.x. Epub 2011 Jun 22.
10
Synaptotagmin Binding to Botulinum Neurotoxins.
Biochemistry. 2020 Feb 4;59(4):491-498. doi: 10.1021/acs.biochem.9b00554. Epub 2019 Dec 18.

引用本文的文献

1
Crystal Structure of CcGH131B, a Protein Belonging to Glycoside Hydrolase Family 131 from the Basidiomycete .
J Appl Glycosci (1999). 2025 May 20;72(2):7202104. doi: 10.5458/jag.7202104. eCollection 2025.
2
Molecular landscape of BoNT/B bound to a membrane-inserted synaptotagmin/ganglioside complex.
Cell Mol Life Sci. 2022 Aug 25;79(9):496. doi: 10.1007/s00018-022-04527-4.
3
Characterization of a membrane binding loop leads to engineering botulinum neurotoxin B with improved therapeutic efficacy.
PLoS Biol. 2020 Mar 17;18(3):e3000618. doi: 10.1371/journal.pbio.3000618. eCollection 2020 Mar.
4
Variations in the Botulinum Neurotoxin Binding Domain and the Potential for Novel Therapeutics.
Toxins (Basel). 2018 Oct 20;10(10):421. doi: 10.3390/toxins10100421.
5
Engineering Botulinum Toxins to Improve and Expand Targeting and SNARE Cleavage Activity.
Toxins (Basel). 2018 Jul 4;10(7):278. doi: 10.3390/toxins10070278.
6
Novel Botulinum Neurotoxins: Exploring Underneath the Iceberg Tip.
Toxins (Basel). 2018 May 10;10(5):190. doi: 10.3390/toxins10050190.
7
Protein Toxins That Utilize Gangliosides as Host Receptors.
Prog Mol Biol Transl Sci. 2018;156:325-354. doi: 10.1016/bs.pmbts.2017.11.010. Epub 2018 Mar 17.
8
A lipid-binding loop of botulinum neurotoxin serotypes B, DC and G is an essential feature to confer their exquisite potency.
PLoS Pathog. 2018 May 2;14(5):e1007048. doi: 10.1371/journal.ppat.1007048. eCollection 2018 May.
9
The Light Chain Defines the Duration of Action of Botulinum Toxin Serotype A Subtypes.
mBio. 2018 Mar 27;9(2):e00089-18. doi: 10.1128/mBio.00089-18.
10
Membrane-Binding Mechanism of Clostridium perfringens Alpha-Toxin.
Toxins (Basel). 2015 Dec 3;7(12):5268-75. doi: 10.3390/toxins7124880.

本文引用的文献

1
Preliminary X-ray crystallographic study of the receptor-binding domain of the D/C mosaic neurotoxin from Clostridium botulinum.
Acta Crystallogr Sect F Struct Biol Cryst Commun. 2010 May 1;66(Pt 5):608-10. doi: 10.1107/S1744309110012182. Epub 2010 Apr 30.
3
Gangliosides as high affinity receptors for tetanus neurotoxin.
J Biol Chem. 2009 Sep 25;284(39):26569-77. doi: 10.1074/jbc.M109.027391. Epub 2009 Jul 14.
4
Glycosylated SV2 and gangliosides as dual receptors for botulinum neurotoxin serotype F.
Biochemistry. 2009 Jun 23;48(24):5631-41. doi: 10.1021/bi9002138.
5
Domain organization in Clostridium botulinum neurotoxin type E is unique: its implication in faster translocation.
J Mol Biol. 2009 Feb 13;386(1):233-45. doi: 10.1016/j.jmb.2008.12.027. Epub 2008 Dec 24.
6
Translocation of botulinum neurotoxin light chain protease by the heavy chain protein-conducting channel.
Toxicon. 2009 Oct;54(5):565-9. doi: 10.1016/j.toxicon.2008.11.018. Epub 2008 Dec 14.
7
Glycosylated SV2A and SV2B mediate the entry of botulinum neurotoxin E into neurons.
Mol Biol Cell. 2008 Dec;19(12):5226-37. doi: 10.1091/mbc.e08-07-0765. Epub 2008 Sep 24.
10
Molecular basis for tetanus toxin coreceptor interactions.
Biochemistry. 2008 Jul 8;47(27):7179-86. doi: 10.1021/bi800640y. Epub 2008 Jun 11.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验