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Updated: Dec 28, 2025

Crystal Structure of the N-terminal Domain of Ryanodine Receptor from Plutella xylostella
Published on: November 30, 2018
Regulatory mechanisms of ryanodine receptor/Ca2+ release channel revealed by recent advancements in structural
Haruo Ogawa1, Nagomi Kurebayashi2, Toshiko Yamazawa3
1Institute for Quantitative Biosciences, The University of Tokyo, Tokyo, 113-0032, Japan. haru@iam.u-tokyo.ac.jp.
Abstract:
Ryanodine receptors (RyRs) are huge homotetrameric Ca2+ release channels localized to the sarcoplasmic reticulum. RyRs are responsible for the release of Ca2+ from the SR during excitation-contraction coupling in striated muscle cells. Recent revolutionary advancements in cryo-electron microscopy have provided a number of near-atomic structures of RyRs, which have enabled us to better understand the architecture of RyRs. Thus, we are now in a new era understanding the gating, regulatory and disease-causing mechanisms of RyRs. Here we review recent advances in the elucidation of the structures of RyRs, especially RyR1 in skeletal muscle, and their mechanisms of regulation by small molecules, associated proteins and disease-causing mutations.
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