| Literature DB >> 25430769 |
Kinga Bercsenyi1, Nathalie Schmieg1, J Barney Bryson2, Martin Wallace1, Paola Caccin3, Matthew Golding4, Giuseppe Zanotti3, Linda Greensmith2, Roswitha Nischt5, Giampietro Schiavo6.
Abstract
Tetanus neurotoxin (TeNT) is among the most poisonous substances on Earth and a major cause of neonatal death in nonvaccinated areas. TeNT targets the neuromuscular junction (NMJ) with high affinity, yet the nature of the TeNT receptor complex remains unknown. Here, we show that the presence of nidogens (also known as entactins) at the NMJ is the main determinant for TeNT binding. Inhibition of the TeNT-nidogen interaction by using small nidogen-derived peptides or genetic ablation of nidogens prevented the binding of TeNT to neurons and protected mice from TeNT-induced spastic paralysis. Our findings demonstrate the direct involvement of an extracellular matrix protein as a receptor for TeNT at the NMJ, paving the way for the development of therapeutics for the prevention of tetanus by targeting this protein-protein interaction.Entities:
Mesh:
Substances:
Year: 2014 PMID: 25430769 DOI: 10.1126/science.1258138
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728