Paudel Bishnu, Rueda David
Department of Medicine, Section of Virology, Imperial College, London, UK.
Methods Mol Biol. 2014;1086:289-307. doi: 10.1007/978-1-62703-667-2_17.
RNA folding pathways can be complex and even include kinetic traps or misfolded intermediates that can be slow to resolve. Characterizing these pathways is critical to understanding how RNA molecules acquire their biological function. We have previously developed a novel approach to help characterize such misfolded intermediates. Laser-assisted single-molecule refolding (LASR) is a powerful technique that combines temperature-jump (T-jump) kinetics with single-molecule detection. In a typical LASR experiment, the temperature is rapidly increased and conformational dynamics are characterized, in real-time, at the single-molecule level using single-molecule fluorescence resonance energy transfer (smFRET). Here, we provide detailed protocols for performing LASR experiments including sample preparation, temperature calibration, and data analysis.
RNA折叠途径可能很复杂,甚至包括动力学陷阱或错误折叠的中间体,这些中间体可能需要很长时间才能解决。表征这些途径对于理解RNA分子如何获得其生物学功能至关重要。我们之前开发了一种新方法来帮助表征此类错误折叠的中间体。激光辅助单分子重折叠(LASR)是一种强大的技术,它将温度跳跃(T-jump)动力学与单分子检测相结合。在典型的LASR实验中,温度会迅速升高,并使用单分子荧光共振能量转移(smFRET)在单分子水平实时表征构象动力学。在这里,我们提供了进行LASR实验的详细方案,包括样品制备、温度校准和数据分析。