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XB-ART-56096
FEBS Lett 2019 Oct 01;59319:2779-2789. doi: 10.1002/1873-3468.13530.
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Scorpion toxins interact with nicotinic acetylcholine receptors.

Kasheverov IE , Oparin PB , Zhmak MN , Egorova NS , Ivanov IA , Gigolaev AM , Nekrasova OV , Serebryakova MV , Kudryavtsev DS , Prokopev NA , Hoang AN , Tsetlin VI , Vassilevski AA , Utkin YN .


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Neurotoxins are among the main components of scorpion and snake venoms. Scorpion neurotoxins affect voltage-gated ion channels, while most snake neurotoxins target ligand-gated ion channels, mainly nicotinic acetylcholine receptors (nAChRs). We report that scorpion venoms inhibit α-bungarotoxin binding to both muscle-type nAChR from Torpedo californica and neuronal human α7 nAChR. Toxins inhibiting nAChRs were identified as OSK-1 (α-KTx family) from Orthochirus scrobiculosus and HelaTx1 (κ-KTx family) from Heterometrus laoticus, both being blockers of voltage-gated potassium channels. With an IC50 of 1.6 μm, OSK1 inhibits acetylcholine-induced current through mouse muscle-type nAChR heterologously expressed in Xenopus oocytes. Other well-characterized scorpion toxins from these families also bind to Torpedo nAChR with micromolar affinities. Our results indicate that scorpion neurotoxins present target promiscuity.

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GO keywords: potassium channel activity