Klebl David P, Aspinall Louie, Muench Stephen P
School of Biomedical Sciences, Astbury Centre for Structural Molecular Biology, University of Leeds, UK.
School of Molecular and Cellular Biology, University of Leeds, UK.
Curr Opin Struct Biol. 2023 Dec;83:102696. doi: 10.1016/j.sbi.2023.102696. Epub 2023 Sep 14.
Developments within the cryo-EM field have allowed us to generate higher-resolution "static" structures and pull out different conformational states which exist at equilibrium within the sample. Moreover, to trap non-equilibrium states and determine conformations that are present after a defined period of time (typically in the ms time frame) new approaches have been developed for the application of time-resolved cryo-EM. Here we give an overview of these different approaches and the limitations and strengths of each whilst identifying some of the current challenges to achieve higher resolutions and trap states within faster time frames. Time-resolved applications may play an important role in the ever-expanding toolkit of cryo-EM and open up new possibilities in both single particle and tomographic studies.
冷冻电镜领域的发展使我们能够生成更高分辨率的“静态”结构,并提取样品中处于平衡状态的不同构象状态。此外,为了捕获非平衡状态并确定在特定时间段(通常在毫秒时间范围内)后存在的构象,已经开发了新的方法用于时间分辨冷冻电镜的应用。在这里,我们概述了这些不同的方法以及每种方法的局限性和优势,同时指出了当前在实现更高分辨率和在更快的时间框架内捕获状态方面面临的一些挑战。时间分辨应用可能在不断扩展的冷冻电镜工具包中发挥重要作用,并为单颗粒和断层扫描研究开辟新的可能性。