Department of Microbiology and of Molecular Genetics, Medical College of Wisconsin,Milwaukee, Wisconsin 53226-3548, USA.
Biochemistry. 2010 Sep 21;49(37):8117-26. doi: 10.1021/bi100865f.
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.
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。