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S100A1 and calmodulin regulation of ryanodine receptor in striated muscle
Authors:Prosser Benjamin L  Hernández-Ochoa Erick O  Schneider Martin F
Institution:aCenter for Biomedical Engineering and Technology (BioMET), University of Maryland, Baltimore, MD 21201, USA;bDepartment of Biochemistry and Molecular Biology, University of Maryland School of Medicine, 108 N. Greene St., Baltimore, MD 21201, USA
Abstract:The release of Ca2+ ions from the sarcoplasmic reticulum through ryanodine receptor calcium release channels represents the critical step linking electrical excitation to muscular contraction in the heart and skeletal muscle (excitation–contraction coupling). Two small Ca2+ binding proteins, S100A1 and calmodulin, have been demonstrated to bind and regulate ryanodine receptor in vitro. This review focuses on recent work that has revealed new information about the endogenous roles of S100A1 and calmodulin in regulating skeletal muscle excitation–contraction coupling. S100A1 and calmodulin bind to an overlapping domain on the ryanodine receptor type 1 to tune the Ca2+ release process, and thereby regulate skeletal muscle function. We also discuss past, current and future work surrounding the regulation of ryanodine receptors by calmodulin and S100A1 in both cardiac and skeletal muscle, and the implications for excitation–contraction coupling.
Keywords:Skeletal muscle  Cardiac muscle  Excitation&ndash  contraction coupling  Dihydropyridine receptors  Voltage-sensors  Transverse tubule  Ryanodine receptor  Sarcoplasmic reticulum  Calcium release  Ca2+-induced Ca2+ release  S100A1  Calmodulin  RyR modulation  Muscular contraction
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