The promise of cryo-EM to explore RNA structural dynamics

被引:24
|
作者
Bonilla, Steve L. [1 ]
Kieft, Jeffrey S. [1 ,2 ,3 ]
机构
[1] Dept Biochem & Mol Genet, Aurora, CO 80045 USA
[2] Univ Colorado Anschutz Med Campus, Sch Med, RNA Biosci Initiat, Aurora, CO 80045 USA
[3] Univ Colorado, Sch Med, Dept Biochem & Mol Genet, Mail Stop 8101, Aurora, CO 80045 USA
基金
美国国家卫生研究院;
关键词
X-RAY-SCATTERING; CRYSTALLIZATION; RECOGNITION; ENSEMBLES; MOTIFS;
D O I
10.1016/j.jmb.2022.167802
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
Conformational dynamics are essential to macromolecular function. This is certainly true of RNA, whose ability to undergo programmed conformational dynamics is essential to create and regulate complex biological processes. However, methods to easily and simultaneously interrogate both the structure and conformational dynamics of fully functional RNAs in isolation and in complex with proteins have not historically been available. Due to its ability to image and classify single particles, cryogenic electron microscopy (cryo-EM) has the potential to address this gap and may be particularly amenable to exploring structural dynamics within the three-dimensional folds of biologically active RNAs. We discuss the possibilities and current limitations of applying cryo-EM to simultaneously study RNA structure and conformational dynamics, and present one example that illustrates this (as of yet) not fully realized potential. (c) 2022 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页数:9
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