Microsecond time-resolved cryo-electron microscopy

被引:5
|
作者
Lorenz, Ulrich J. [1 ]
机构
[1] Ecole Polytech Fed Lausanne EPFL, Lab Mol Nanodynam, CH-1015 Lausanne, Switzerland
基金
瑞士国家科学基金会;
关键词
Time-resolved cr yo-electron microscopy; Cr yo-electron microscopy; Protein dynamics; Melting and revitrification; CHLOROTIC MOTTLE VIRUS; STRUCTURAL BIOLOGY; CRYO-EM; PROTEIN; DYNAMICS;
D O I
10.1016/j.sbi.2024.102840
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
Microsecond time-resolved cryo-electron microscopy has emerged as a novel approach for directly observing protein dynamics. By providing microsecond temporal and nearatomic spatial resolution, it has the potential to elucidate a wide range of dynamics that were previously inaccessible and therefore, to significantly advance our understanding of protein function. This review summarizes the properties of the laser melting and revitrification process that underlies the technique and describes different experimental implementations. Strategies for initiating and probing dynamics are discussed. Finally, the microsecond time-resolved observation of the capsid dynamics of cowpea chlorotic mottle virus, an icosahedral plant virus, is reviewed, which illustrates important features of the technique as well as its potential.
引用
收藏
页数:7
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