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Integrative approaches in cryogenic electron microscopy: Recent advances in structural biology and future perspectives

机译:低温电子显微镜的一体化方法:结构生物学和未来观点的最新进展

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摘要

Cellular factories engage numerous highly complex “molecular machines” to perform pivotal biological functions. 3D structural visualization is an effective way to understand the functional mechanisms of these biomacromolecules. The “resolution revolution” has established cryogenic electron microscopy (cryo-EM) as a preferred structural biology tool. In parallel with the advances in cryo-EM methodologies aiming at atomic resolution, several innovative approaches have started emerging where other techniques are sensibly integrated with cryo-EM to obtain additional insights into the biological processes. For example, combining the time-resolved technique with high-resolution cryo-EM enables discerning structures of short-lived intermediates in the functional pathway of a biomolecule. Likewise, integrating mass spectrometry (MS) techniques with cryo-EM allows deciphering structural organizations of large molecular assemblies. Here, we discuss how the data generated upon combining either time resolve or MS techniques with cryo-EM supplement structural elucidations with in-depth understanding of the function of cellular macromolecules when they participate in fundamental biological processes.
机译:蜂窝工厂从事许多高度复杂的“分子机器”以进行枢转生物学功能。 3D结构可视化是理解这些生物致摩托的功能机制的有效方法。 “分辨率革命”已经建立了低温电子显微镜(Cryo-EM)作为优选的结构生物学工具。与针对原子分辨率的冷冻 - EM方法的进展并行,若干创新方法已经开始出现,其中其他技术与Cryo-EM明智地集成,以获得对生物过程的额外见解。例如,将具有高分辨率冷冻系统的时间分辨技术组合使得能够在生物分子的功能途径中辨别出短寿命的中间体的结构。同样地,将质谱(MS)技术与Cryo-EM相同允许解密大分子组件的结构组织。在这里,我们讨论如何在组合时产生的数据与Cryo-EM补充结构阐明组合或MS技术,以便在参与基本生物过程时对细胞大分子的功能进行深入理解。

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