Single Molecule Analysis Group and Center for RNA Biomedicine, Department of Chemistry , University of Michigan , Ann Arbor , Michigan 48109 , United States.
Chem Rev. 2018 Apr 25;118(8):4120-4155. doi: 10.1021/acs.chemrev.7b00519. Epub 2018 Jan 24.
The emergence of single-molecule (SM) fluorescence techniques has opened up a vast new toolbox for exploring the molecular basis of life. The ability to monitor individual biomolecules in real time enables complex, dynamic folding pathways to be interrogated without the averaging effect of ensemble measurements. In parallel, modern biology has been revolutionized by our emerging understanding of the many functions of RNA. In this comprehensive review, we survey SM fluorescence approaches and discuss how the application of these tools to RNA and RNA-containing macromolecular complexes in vitro has yielded significant insights into the underlying biology. Topics covered include the three-dimensional folding landscapes of a plethora of isolated RNA molecules, their assembly and interactions in RNA-protein complexes, and the relation of these properties to their biological functions. In all of these examples, the use of SM fluorescence methods has revealed critical information beyond the reach of ensemble averages.
单分子(SM)荧光技术的出现为探索生命的分子基础开辟了一个广阔的新工具包。实时监测单个生物分子的能力使我们能够在没有整体测量平均效应的情况下探究复杂的、动态的折叠途径。与此同时,我们对 RNA 的多种功能的认识也正在彻底改变现代生物学。在这篇全面的综述中,我们调查了 SM 荧光方法,并讨论了这些工具在体外 RNA 和含有 RNA 的大分子复合物中的应用如何为基础生物学提供了重要的见解。涵盖的主题包括大量分离 RNA 分子的三维折叠景观、它们在 RNA-蛋白质复合物中的组装和相互作用,以及这些特性与其生物学功能的关系。在所有这些例子中,SM 荧光方法的使用揭示了超越整体平均值的关键信息。