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近期结构研究进展揭示的兰尼碱受体/钙释放通道的调控机制。

Regulatory mechanisms of ryanodine receptor/Ca release channel revealed by recent advancements in structural studies.

机构信息

Institute for Quantitative Biosciences, The University of Tokyo, Tokyo, 113-0032, Japan.

Department of Pharmacology, Juntendo University School of Medicine, Tokyo, 113-8421, Japan.

出版信息

J Muscle Res Cell Motil. 2021 Jun;42(2):291-304. doi: 10.1007/s10974-020-09575-6. Epub 2020 Feb 10.

Abstract

Ryanodine receptors (RyRs) are huge homotetrameric Ca release channels localized to the sarcoplasmic reticulum. RyRs are responsible for the release of Ca 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.

摘要

肌质网钙释放通道(Ryanodine receptors,RyRs)是巨大的同源四聚体 Ca 释放通道,定位于肌质网。在横纹肌细胞的兴奋-收缩偶联过程中,RyRs 负责从肌质网中释放 Ca。最近冷冻电子显微镜技术的革命性进展提供了许多 RyRs 的近原子结构,使我们能够更好地理解 RyRs 的结构。因此,我们现在正处于一个理解 RyRs 的门控、调节和致病变异机制的新时代。本文综述了 RyRs 结构,尤其是骨骼肌 RyR1 结构阐明的最新进展,以及小分子、相关蛋白和致病变异对 RyRs 调节的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acdd/8332584/51404cf0bc37/10974_2020_9575_Fig1_HTML.jpg

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