Bridging the myoplasmic gap: recent developments in skeletal muscle excitation-contraction coupling

被引：31

作者：

Bannister, Roger A. ^{[1
]}

机构：

[1] Univ Colorado, Sch Med, Denver & Hlth Sci Ctr, Dept Physiol & Biophys, Aurora, CO 80045 USA

来源：

JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY | 2007年 / 28卷 / 4-5期

关键词：

DHPR; alpha; 1S; Ca(V)1.1; beta; 1a; RyR1; L-type; excitation-contraction coupling; skeletal muscle;

D O I：

10.1007/s10974-007-9118-5

中图分类号：

Q2 [细胞生物学];

学科分类号：

071009 ; 090102 ;

摘要：

Conformational coupling between the L-type voltage-gated Ca2+ channel (or 1,4-dihydropyridine receptor; DHPR) and the ryanodine-sensitive Ca2+ release channel of the sarcoplasmic reticulum (RyR1) is the mechanistic basis for excitation-contraction (EC) coupling in skeletal muscle. In this article, recent findings regarding the roles of the individual cytoplasmic domains (the amino- and carboxyl-termini, cytoplasmic loops I-II, II-III, and III-IV) of the DHPR alpha(1S) subunit in bi-directional communication with RyR1 will be discussed.

引用

页码：275 / 283

页数：9

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