2+ from the endoplasmic or sarcoplasmic reticulum. They are expressed in many different cell types but ar'/> The structural biology of ryanodine receptors
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The structural biology of ryanodine receptors

机译:ryanodine受体的结构生物学

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Ryanodine receptors are ion channels that allow for the release of Ca2+ from the endoplasmic or sarcoplasmic reticulum. They are expressed in many different cell types but are best known for their predominance in skeletal and cardiac myocytes, where they are directly involved in excitation-contraction coupling. With molecular weights exceeding 2 MDa, Ryanodine Receptors are the largest ion channels known to date and present major challenges for structural biology. Since their discovery in the 1980s, significant progress has been made in understanding their behaviour through multiple structural methods. Cryo-electron microscopy reconstructions of intact channels depict a mushroom-shaped structure with a large cytoplasmic region that presents many binding sites for regulatory molecules. This region undergoes significant motions during opening and closing of the channel, demonstrating that the Ryanodine Receptor is a bona fide allosteric protein. High-resolution structures through X-ray crystallography and NMR currently cover ~11% of the entire protein. The combination of high- and low-resolution methods allows us to build pseudo-atomic models. Here we present an overview of the electron microscopy, NMR, and crystallographic analyses of this membrane protein giant.
机译:Ryanodine受体是离子通道,可从内质网或肌浆网释放Ca 2 + 。它们在许多不同的细胞类型中表达,但最著名的是它们在骨骼肌和心肌细胞中的优势,它们直接参与激发-收缩偶联。 Ryanodine受体的分子量超过2 MDa,是迄今为止已知的最大离子通道,对结构生物学提出了重大挑战。自从1980年代发现它们以来,通过多种结构方法来了解它们的行为已取得了重大进展。完整通道的低温电子显微镜重建显示出蘑菇形结构,具有大的胞质区域,呈现出许多调控分子的结合位点。该区域在通道的打开和关闭过程中经历了明显的运动,表明Ryanodine受体是真正的变构蛋白。通过X射线晶体学和NMR鉴定的高分辨率结构目前覆盖了整个蛋白质的约11%。高分辨率和低分辨率方法的组合使我们能够构建伪原子模型。在这里,我们介绍了此膜蛋白巨人的电子显微镜,NMR和晶体学分析的概述。

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