Ryanodine receptor calcium release channels: lessons from structure-function studies

被引:51
作者
Amador, Fernando J.
Stathopulos, Peter B.
Enomoto, Masahiro
Ikura, Mitsuhiko [1 ,2 ]
机构
[1] Univ Toronto, Ontario Canc Inst, Toronto, ON M5G 1L7, Canada
[2] Univ Toronto, Dept Med Biophys, Toronto, ON M5G 1L7, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
cryo-electron microscopy; excitation-contraction coupling; inositol; 1; 4; 5-trisphosphate receptor; malignant hyperthermia; nuclear magnetic resonance spectroscopy; ryanodine receptor; X-ray crystallography; II-III LOOP; INOSITOL 1,4,5-TRISPHOSPHATE RECEPTORS; POLYMORPHIC VENTRICULAR-TACHYCARDIA; CENTRAL CORE DISEASE; INDUCED CA2+ RELEASE; SKELETAL-MUSCLE; DIHYDROPYRIDINE RECEPTOR; MALIGNANT HYPERTHERMIA; CALMODULIN-BINDING; SARCOPLASMIC-RETICULUM;
D O I
10.1111/febs.12194
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ryanodine receptors (RyRs) are the largest known ion channels. They are Ca2+ release channels found primarily on the sarcoplasmic reticulum of myocytes. Several hundred mutations in RyRs are associated with skeletal or cardiomyocyte disease in humans. Many of these mutations can now be mapped onto the high resolution structures of individual RyR domains and on full-length tetrameric cryo-electron microscopy structures. A closely related Ca2+ release channel, the inositol 1,4,5-trisphospate receptor (IP3R), shows a conserved structural architecture at the N-terminus, suggesting that both channels evolved from an ancestral unicellular RyR/IP3R. The functional insights provided by recent structural studies for both channels will aid in the development of rationale treatments for a myriad of Ca2+-signaled malignancies.
引用
收藏
页码:5456 / 5470
页数:15
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