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Ligand-induced activation of RyR1 in native membranes

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Item Type:Article
Title:Ligand-induced activation of RyR1 in native membranes
Creators: Mikirtumov, Vasilii ORCID logoORCID: https://orcid.org/0009-0004-6849-4825, Golusik, Sabrina, Huo, Ruifeng ORCID logoORCID: https://orcid.org/0009-0001-4915-150X, Sprink, Thiemo ORCID logoORCID: https://orcid.org/0000-0002-0760-6828, Balyschew, Nikita, Yang, Wen, Diebolder, Christoph ORCID logoORCID: https://orcid.org/0000-0001-7694-7362, Yuan, Shuguang ORCID logoORCID: https://orcid.org/0000-0001-9858-4742, Kotecha, Abhay and Kudryashev, Mikhail ORCID logoORCID: https://orcid.org/0000-0003-3550-6274
Abstract:Synchronized calcium release through arrays of the ryanodine receptor RyR1, fundamental to skeletal muscle excitation-contraction coupling, is achieved through the mechanical interaction of RyR1s and voltage-sensing receptors DHPR that activate RyR1s in response to action potentials. The calcium release is enhanced through “coupled gating”, when the activation of one channel promotes the opening of its neighbours. Here, we determine high-resolution structures of RyR1 in native sarcoplasmic reticulum membranes by cryo-EM/ET, capturing the conformations along the activation pathway and corner-to-corner interfaces between adjacent RyR1 receptors. Compared with purified RyR1s, receptors in native membranes follow an activation pathway with reduced cytosolic-shell tilt and greater consecutive in-plane rotation. Activation-induced rotation remodels the inter-receptor interface, lowering the energy barrier to the cooperative opening of the receptor cluster. Our analysis demonstrates how the native membrane receptor lattice influences ion channel cluster dynamics and provides a mechanistic framework for understanding calcium signaling in muscle.
Keywords:Calcium, Calcium Signaling, Cryoelectron Microscopy, Ion Channel Gating, Ligands, Ryanodine Receptor Calcium Release Channel, Sarcoplasmic Reticulum, Skeletal Muscle, Animals
Source:Nature Communications
ISSN:2041-1723
Publisher:Nature Publishing Group
Volume:17
Number:1
Page Range:10075
Date:24 September 2026
Official Publication:https://doi.org/10.1038/s41467-026-75504-9
PubMed:View item in PubMed

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