Spider toxin inhibits gating pore currents underlying periodic paralysis

Proceedings of the National Academy of Sciences of the United States of America
Roope MännikköAlexander A Vassilevski

Abstract

Gating pore currents through the voltage-sensing domains (VSDs) of the skeletal muscle voltage-gated sodium channel NaV1.4 underlie hypokalemic periodic paralysis (HypoPP) type 2. Gating modifier toxins target ion channels by modifying the function of the VSDs. We tested the hypothesis that these toxins could function as blockers of the pathogenic gating pore currents. We report that a crab spider toxin Hm-3 from Heriaeus melloteei can inhibit gating pore currents due to mutations affecting the second arginine residue in the S4 helix of VSD-I that we have found in patients with HypoPP and describe here. NMR studies show that Hm-3 partitions into micelles through a hydrophobic cluster formed by aromatic residues and reveal complex formation with VSD-I through electrostatic and hydrophobic interactions with the S3b helix and the S3-S4 extracellular loop. Our data identify VSD-I as a specific binding site for neurotoxins on sodium channels. Gating modifier toxins may constitute useful hits for the treatment of HypoPP.

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Citations

Aug 23, 2018·Frontiers in Pharmacology·Denis B Tikhonov, Boris S Zhorov
Apr 24, 2019·Doklady. Biochemistry and Biophysics·Z O ShenkarevM P Kirpichnikov
Dec 17, 2020·Journal of Neuromuscular Diseases·Jean-François DesaphyBertrand Fontaine
Apr 2, 2021·Journal of Molecular Biology·Sigrid NorengJian Payandeh

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