Time resolved applications for Cryo-EM; approaches, challenges and future directions

被引:6
|
作者
Klebl, David P. [1 ]
Aspinall, Louie [2 ]
Muench, Stephen P. [1 ]
机构
[1] Univ Leeds, Astbury Ctr Struct Mol Biol, Sch Biomed Sci, Leeds, England
[2] Univ Leeds, Sch Mol & Cellular Biol, Leeds, England
基金
英国生物技术与生命科学研究理事会;
关键词
Time-resolved; Cryo-EM; Sample preparation; Protein dynamics; CRYOELECTRON MICROSCOPY; GRID PREPARATION; ENDOCYTOSIS;
D O I
10.1016/j.sbi.2023.102696
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 cryoEM. 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.
引用
收藏
页数:7
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