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Structural Analysis of Botulinum Neurotoxin Type G Receptor Binding
- Source :
- Biochemistry. 49:5200-5205
- Publication Year :
- 2010
- Publisher :
- American Chemical Society (ACS), 2010.
-
Abstract
- Botulinum neurotoxin (BoNT) binds peripheral neurons at the neuromuscular junction through a dual-receptor mechanism that includes interactions with ganglioside and protein receptors. The receptor identities vary depending on BoNT serotype (A-G). BoNT/B and BoNT/G bind the luminal domains of Synaptotagmin (Syt)-I and SytII, homologous synaptic vesicle proteins. We observe conditions in which BoNT/B binds both Syt isoforms, but BoNT/G only binds SytI. Both serotypes bind ganglioside GT1b. The BoNT/G receptor-binding domain crystal structure provides a context for examining these binding interactions and a platform to understand the physiological relevance of different Syt receptor isoforms in vivo.
- Subjects :
- Models, Molecular
Botulinum Toxins
Ganglioside
Protein Conformation
Genetic Vectors
Synaptotagmin I
Receptors, Cell Surface
Context (language use)
Plasma protein binding
Biology
Crystallography, X-Ray
Biochemistry
Molecular biology
Synaptic vesicle
Article
Neuromuscular junction
medicine.anatomical_structure
Protein structure
Gangliosides
medicine
Receptor
Protein Binding
Subjects
Details
- ISSN :
- 15204995 and 00062960
- Volume :
- 49
- Database :
- OpenAIRE
- Journal :
- Biochemistry
- Accession number :
- edsair.doi.dedup.....2d3e8fe994aa3468f2c547fdd5b84637
- Full Text :
- https://doi.org/10.1021/bi100412v