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Updated: Feb 12, 2026

Crystal Structure of the N-terminal Domain of Ryanodine Receptor from Plutella xylostella
Published on: November 30, 2018
Structural Details of the Ryanodine Receptor Calcium Release Channel and Its Gating Mechanism
Katrien Willegems1,2, Rouslan G Efremov3,4
1Center for Structural Biology, Vlaams Instituut voor Biotechnologie, Brussels, Belgium.
Abstract:
Ryanodine receptors (RyRs) are large intracellular calcium release channels that play a crucial role in coupling excitation to contraction in both cardiac and skeletal muscle cells. In addition, they are expressed in other cell types where their function is less well understood. Hundreds of mutations in the different isoforms of RyR have been associated with inherited myopathies and cardiac arrhythmia disorders. The structure of these important drug targets remained elusive for a long time, despite decades of intensive research. In the recent years, a technical revolution in the field of single particle cryogenic electron microscopy (SP cryo-EM) allowed solving high-resolution structures of the skeletal and cardiac RyR isoforms. Together with the structures of individual domains solved by X-ray crystallography, this resulted in an unprecedented understanding of the structure, gating and regulation of these largest known ion channels. In this chapter we describe the recently solved high-resolution structures of RyRs, discuss molecular details of the channel gating, regulation and the disease mutations. Additionally, we highlight important questions that require further progress in structural studies of RyRs.
Insights
Ryanodine receptors (RyRs), crucial calcium channels, are now understood at high resolution thanks to cryo-EM. This breakthrough reveals insights into their structure, function, and disease-related mutations.
Area of Science:
- Biophysics
- Molecular Biology
- Structural Biology
Background:
- Ryanodine receptors (RyRs) are critical intracellular calcium release channels.
- Mutations in RyRs are linked to muscle and heart disorders.
- High-resolution structures of RyRs were previously unavailable.
Purpose of the Study:
- To describe recent high-resolution structures of RyRs.
- To discuss RyR gating, regulation, and disease mutations.
- To identify future research directions for RyR structural studies.
Main Methods:
- Single particle cryogenic electron microscopy (SP cryo-EM) for full channel structures.
- X-ray crystallography for individual domain structures.
Main Results:
- High-resolution structures of skeletal and cardiac RyR isoforms have been solved.
- Detailed understanding of RyR structure, gating, and regulation is now possible.
- Molecular basis of disease-associated mutations can be investigated.
Conclusions:
- SP cryo-EM has revolutionized RyR structural biology.
- Understanding RyR structure provides insights into muscle excitation-contraction coupling.
- Further structural studies are needed to address remaining questions about RyR function and disease.
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