Pljevaljčić Goran, Robertson-Anderson Rae, van der Schans Edwin, Millar David
Department of Molecular Biology, The Scripps Research Institute, La Jolla, CA, USA.
Methods Mol Biol. 2012;875:271-95. doi: 10.1007/978-1-61779-806-1_15.
To execute their diverse range of biological functions, RNA molecules must fold into specific tertiary structures and/or associate with one or more proteins to form ribonucleoprotein (RNP) complexes. Single-molecule fluorescence spectroscopy is a powerful tool for the study of RNA folding and RNP assembly processes, directly revealing different conformational subpopulations that are hidden in conventional ensemble measurements. Moreover, kinetic processes can be observed without the need to synchronize a population of molecules. In this chapter, we describe the fluorescence spectroscopic methods used for single-molecule measurements of freely diffusing or immobilized RNA molecules or RNA-protein complexes. We also provide practical protocols to prepare the fluorescently labeled RNA and protein molecules required for such studies. Finally, we provide two examples of how these various preparative and spectroscopic methods are employed in the study of RNA folding and RNP assembly processes.
为了执行其多种多样的生物学功能,RNA分子必须折叠成特定的三级结构和/或与一种或多种蛋白质结合形成核糖核蛋白(RNP)复合物。单分子荧光光谱法是研究RNA折叠和RNP组装过程的有力工具,它能直接揭示传统整体测量中隐藏的不同构象亚群。此外,无需同步分子群体就能观察动力学过程。在本章中,我们描述了用于对自由扩散或固定化的RNA分子或RNA-蛋白质复合物进行单分子测量的荧光光谱方法。我们还提供了实用的实验方案,以制备此类研究所需的荧光标记RNA和蛋白质分子。最后,我们给出两个例子,说明这些不同的制备和光谱方法如何用于RNA折叠和RNP组装过程的研究。