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
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