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结构动力学:时间分辨冷冻电镜综述。

Structural dynamics: review of time-resolved cryo-EM.

机构信息

The Visual Biochemistry Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, United Kingdom.

出版信息

Acta Crystallogr D Struct Biol. 2022 Aug 1;78(Pt 8):927-935. doi: 10.1107/S2059798322006155. Epub 2022 Jul 21.

Abstract

The structural determination of biological macromolecules has been transformative for understanding biochemical mechanisms and developing therapeutics. However, the ultimate goal of characterizing how structural dynamics underpin biochemical processes has been difficult. This is largely due to significant technical challenges that hinder data collection and analysis on the native timescales of macromolecular dynamics. Single-particle cryo-EM provides a powerful platform to approach this challenge, since samples can be frozen faster than the single-turnover timescales of most biochemical reactions. In order to enable time-resolved analysis, significant innovations in the handling and preparation of cryo-EM samples have been implemented, bringing us closer to the goal of the direct observation of protein dynamics in the milliseconds to seconds range. Here, the current state of time-resolved cryo-EM is reviewed and the most promising future research directions are discussed.

摘要

生物大分子的结构测定对于理解生化机制和开发治疗方法具有变革性。然而,表征结构动力学如何为生化过程提供支撑的最终目标一直难以实现。这主要是由于在生物大分子动力学的天然时间尺度上,数据收集和分析存在重大技术挑战。单颗粒冷冻电镜提供了一个强大的平台来解决这个挑战,因为样品可以在比大多数生化反应的单轮时间尺度更快的速度下冷冻。为了实现时间分辨分析,已经在冷冻电镜样品的处理和制备方面进行了重大创新,使我们更接近在毫秒到秒的范围内直接观察蛋白质动力学的目标。在这里,回顾了时间分辨冷冻电镜的现状,并讨论了最有前途的未来研究方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d2b/9344476/e0ddf19e7351/d-78-00927-fig1.jpg

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