Structural dynamics: review of time-resolved cryo-EM

被引:24
|
作者
Maeots, Mart-Erik [1 ]
Enchev, Radoslav, I [1 ]
机构
[1] Francis Crick Inst, Visual Biochem Lab, 1 Midland Rd, London NW1 1AT, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
cryo-EM; time-resolved cryo-EM; sample preparation; structural biology; structural dynamics; CRYOELECTRON MICROSCOPY; ELECTRON CRYOMICROSCOPY; GRID PREPARATION; DEVICE; VITRIFICATION; APPARATUS; MOVEMENT; SPOTITON;
D O I
10.1107/S2059798322006155
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:927 / 935
页数:9
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