| Literature DB >> 20731382 |
Andrew P-A Karalewitz1, Abby R Kroken, Zhuji Fu, Michael R Baldwin, Jung-Ja P Kim, Joseph T Barbieri.
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.Entities:
Mesh:
Substances:
Year: 2010 PMID: 20731382 PMCID: PMC2939319 DOI: 10.1021/bi100865f
Source DB: PubMed Journal: Biochemistry ISSN: 0006-2960 Impact factor: 3.162