The tarantula toxin jingzhaotoxin-XI (κ-theraphotoxin-Cj1a) regulates the activation and inactivation of the voltage-gated sodium channel Nav1.5-Reference-Cited by-同舟云学术

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The tarantula toxin jingzhaotoxin-XI (κ-theraphotoxin-Cj1a) regulates the activation and inactivation of the voltage-gated sodium channel Nav1.5

Published:2014-12 Issue: Volume:92 Page:6-13
ISSN:0041-0101
Container-title:Toxicon
language:en
Short-container-title:Toxicon

Author:

Tang Cheng,Zhou Xi,Huang Yin,Zhang Yunxiao,Hu Zhaotun,Wang Meichi,Chen Ping,Liu Zhonghua,Liang Songping

Funder

National Basic Research Program of China

National Science Foundation

Cooperative Innovation Center of Engineering and New Products for Developmental Biology of Hunan Province

Publisher

Elsevier BV

Subject

Toxicology

Reference41 articles.

1. Na channel inactivation from open and closed states;Armstrong;Proc. Natl. Acad. Sci. U. S. A.,2006

2. Mechanisms of closed-state inactivation in voltage-gated ion channels;Bähring;J. Physiol.,2011

3. Activation and inactivation of the voltage-gated sodium channel: role of segment S5 revealed by a novel hyperkalaemic periodic paralysis mutation;Bendahhou;J. Neurosci. Off. J. Soc. Neurosci.,1999

4. Animal peptides targeting voltage-activated sodium channels;Billen;Curr. Pharm. Des.,2008

5. Unique bell-shaped voltage-dependent modulation of Na+ channel gating by novel insect-selective toxins from the spider Agelena orientalis;Billen;J. Biol. Chem.,2010

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1. LmNaTx15, a novel scorpion toxin, enhances the activity of Nav channels and induces pain in mice;Toxicon;2023-12

2. Structure-function relationship of new peptides activating human Nav1.1;Biomedicine & Pharmacotherapy;2023-09

3. A Novel Spider Toxin Inhibits Fast Inactivation of the Nav1.9 Channel by Binding to Domain III and Domain IV Voltage Sensors;Frontiers in Pharmacology;2021-12-06

4. Spider Knottin Pharmacology at Voltage-Gated Sodium Channels and Their Potential to Modulate Pain Pathways;Toxins;2019-10-29

5. Animal toxins for channelopathy treatment;Neuropharmacology;2018-04

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