Structure of the voltage-gated calcium channel Cav1.1 complex

被引:243
作者
Wu, Jianping [1 ,2 ,3 ,4 ]
Yan, Zhen [1 ,2 ,3 ,4 ]
Li, Zhangqiang [1 ,2 ,3 ,4 ]
Yan, Chuangye [1 ,2 ,3 ,4 ]
Lu, Shan [5 ]
Dong, Mengqiu [5 ]
Yan, Nieng [1 ,2 ,3 ,4 ]
机构
[1] Tsinghua Univ, State Key Lab Membrane Biol, Beijing 100084, Peoples R China
[2] Tsinghua Univ, Tsinghua Peking Joint Ctr Life Sci, Beijing 100084, Peoples R China
[3] Tsinghua Univ, Sch Life Sci, Struct Biol Ctr, Beijing 100084, Peoples R China
[4] Tsinghua Univ, Sch Med, Beijing 100084, Peoples R China
[5] Natl Inst Biol Sci, Beijing 102206, Peoples R China
关键词
CA2+ CHANNEL; CRYSTAL-STRUCTURE; SKELETAL-MUSCLE; DIHYDROPYRIDINE RECEPTOR; BETA-SUBUNIT; DOMAIN; INSIGHT; IDENTIFICATION; ALPHA(2)DELTA; VISUALIZATION;
D O I
10.1126/science.aad2395
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The voltage-gated calcium channel Cav1.1 is engaged in the excitation-contraction coupling of skeletal muscles. The Cav1.1 complex consists of the pore-forming subunit α1 and auxiliary subunits α2δ, β, and γ. We report the structure of the rabbit Cav1.1 complex determined by single-particle cryo-electron microscopy. The four homologous repeats of the α1 subunit are arranged clockwise in the extracellular view. The γ subunit, whose structure resembles claudins, interacts with the voltage-sensing domain of repeat IV (VSDIV), whereas the cytosolic β subunit is located adjacent to VSDII of α1. The α2 subunit interacts with the extracellular loops of repeats I to III through its VWA and Cache1 domains. The structure reveals the architecture of a prototypical eukaryotic Cav channel and provides a framework for understanding the function and disease mechanisms of Cav and Nav channels.
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页数:10
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