版权说明 操作指南
首页 > 成果 > 详情

Molecular basis of the inhibition of the fast inactivation of voltage-gated sodium channel Nav1.5 by tarantula toxin Jingzhaotoxin-II

认领
导出
Link by DOI
反馈
分享
QQ微信 微博
成果类型:
期刊论文
作者:
Huang, Ying;Zhou, Xi(周曦);Tang, Cheng;Zhang, Yunxiao;Tao, Huai(陶怀);...
通讯作者:
Liu, ZH
作者机构:
[Zhou, Xi; Tang, Cheng; Chen, Ping; Zhang, Yunxiao; Liu, Zhonghua; Huang, Ying] Hunan Normal Univ, Coll Life Sci, Changsha 410081, Hunan, Peoples R China.
[Tao, Huai] Hunan Univ Chinese Med, Dept Biochem & Mol Biol, Changsha 410208, Hunan, Peoples R China.
通讯机构:
[Liu, ZH ] H
Hunan Normal Univ, Coll Life Sci, Changsha 410081, Hunan, Peoples R China.
语种:
英文
关键词:
jingzhaotoxin-II, Chilobrachys jingzhao;Scn5a protein, rat;sodium channel blocking agent;sodium channel Nav1.5;spider venom;amino acid sequence;animal;binding site;chemistry;drug effects;HEK293 cell line;human;kinetics;membrane potential;metabolism;molecular genetics;protein domain;rat;Amino Acid Sequence;Animals;Binding Sites;HEK293 Cells;Humans;Kinetics;Membrane Potentials;Molecular Sequence Data;NAV1.5 Voltage-Gated Sodium Channel;Protein Interaction Domains and Motifs;Rats;Sodium Channel Blockers;Spider Venoms
期刊:
Peptides
ISSN:
0196-9781
年:
2015
卷:
68
页码:
175-182
基金类别:
This work was supported by the National Basic Research Program of China (973 Program), grant No. 2010CB529801; the National Science Foundation Project, grant Nos. 31370783 and 31370817; the Science Found for Distinguished Young Scholars of Hunan Province (No. 14JJ1018); and the Cooperative Innovation Center of Engineering and New Products for Developmental Biology of Hunan Province (grant No. 20134486).
机构署名:
本校为其他机构
院系归属:
医学院
中医学院
摘要:
Jingzhaotoxin-II (JZTX-II) is a 32-residue peptide from the Chinese tarantula Chilobrachys jingzhao venom, and preferentially inhibits the fast inactivation of the voltage-gated sodium channels (VGSCs) in rat cardiac myocytes. In the present study, we elucidated the action mechanism of JZTX-II inhibiting hNav1.5, a VGSC subtype mainly distributed in human cardiac myocytes. Among the four VGSC subtypes tested, hNav1.5 was the most sensitive to JZTX-II (EC50 = 125 ± 4 nM). Although JZTX-II had little or no effect on steady-state inactivation of ...

反馈

验证码:
看不清楚,换一个
确定
取消

成果认领

标题:
用户 作者 通讯作者
请选择
请选择
确定
取消

提示

该栏目需要登录且有访问权限才可以访问

如果您有访问权限,请直接 登录访问

如果您没有访问权限,请联系管理员申请开通

管理员联系邮箱:yun@hnwdkj.com