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电子冷冻显微镜和 X 射线晶体学的互补应用:肌动蛋白和肌球蛋白丝的结构研究。

Complementary Use of Electron Cryomicroscopy and X-Ray Crystallography: Structural Studies of Actin and Actomyosin Filaments.

机构信息

Graduate School of Frontier Biosciences, Osaka University, Suita, Osaka, Japan.

Quantitative Biology Center, Riken, Osaka, Japan.

出版信息

Adv Exp Med Biol. 2018;1105:25-42. doi: 10.1007/978-981-13-2200-6_4.

Abstract

Visualization of macromolecular structures is essential for understanding the mechanisms of biological functions because they are all determined by the structure and dynamics of macromolecular complexes. Electron cryomicroscopy (cryoEM) and image analysis has become a powerful tool for structural studies because of recent technical developments in microscope optics, cryostage control, image detection and the methods of sample preparation. In particular, the recent development of CMOS-based direct electron detectors with high sensitivity, high resolution and high frame rate has revolutionized the field of structural biology by making near-atomic resolution structural analysis possible from small amounts of solution samples. However, for some biological systems, it is still difficult to reach high resolution due to somewhat flexible nature of the structure, and a complementary use of cryoEM with X-ray crystallography is essential and useful to gain mechanistic understanding of the biological functions and mechanisms. We will describe our strategy for the structural analyses of actin filament and actomyosin rigor complex and the biological insights we gained from these structures.

摘要

大分子结构的可视化对于理解生物功能的机制至关重要,因为它们都是由大分子复合物的结构和动力学决定的。电子晶体学显微镜(cryoEM)和图像分析已经成为结构研究的有力工具,这要归功于显微镜光学、低温控制、图像检测和样品制备方法的最新技术发展。特别是,基于 CMOS 的直接电子探测器具有高灵敏度、高分辨率和高帧率的特点,这使得从小量溶液样品中进行近原子分辨率结构分析成为可能,从而彻底改变了结构生物学领域。然而,对于某些生物系统,由于结构的某种灵活性,仍然难以达到高分辨率,因此,与 X 射线晶体学互补使用对于获得对生物功能和机制的理解是至关重要和有用的。我们将描述我们用于肌动蛋白丝和肌球蛋白僵硬复合物的结构分析的策略,以及我们从这些结构中获得的生物学见解。

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