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兰尼碱受体钙释放通道的结构细节及其门控机制。

Structural Details of the Ryanodine Receptor Calcium Release Channel and Its Gating Mechanism.

机构信息

Center for Structural Biology, Vlaams Instituut voor Biotechnologie, Brussels, Belgium.

Structural Biology Brussels, Department of Bioengineering Sciences, Vrije Universiteit Brussel, Brussels, Belgium.

出版信息

Adv Exp Med Biol. 2017;981:179-204. doi: 10.1007/978-3-319-55858-5_8.

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.

摘要

兰尼碱受体(Ryanodine receptors,RyRs)是一种大型的细胞内钙离子释放通道,在心脏和骨骼肌细胞中,它在兴奋-收缩耦联过程中发挥着关键作用。此外,它还在其他细胞类型中表达,但这些细胞类型中 RyR 的功能尚不清楚。数百种 RyR 的不同亚型的突变与遗传性肌病和心律失常疾病有关。尽管经过几十年的深入研究,这些重要药物靶点的结构仍然难以捉摸。近年来,单颗粒冷冻电子显微镜(single particle cryogenic electron microscopy,SP cryo-EM)领域的技术革命使得解决骨骼肌和心脏 RyR 同工型的高分辨率结构成为可能。与 X 射线晶体学解析的各个结构域的结构相结合,这导致了对这些已知最大的离子通道的结构、门控和调节的空前理解。在本章中,我们描述了最近解决的 RyR 的高分辨率结构,讨论了通道门控、调节和疾病突变的分子细节。此外,我们还强调了需要在 RyR 的结构研究中进一步取得进展的重要问题。

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