Cheng Chao-Han, Ishii Kunihiko, Tahara Tahei
Molecular Spectroscopy Laboratory, RIKEN, 2-1 Hirosawa, Wako 351-0198, Japan.
Ultrafast Spectroscopy Research Team, RIKEN Center for Advanced Photonics (RAP), 2-1 Hirosawa, Wako 351-0198, Japan.
J Phys Chem B. 2020 Nov 25;124(47):10673-10681. doi: 10.1021/acs.jpcb.0c07600. Epub 2020 Nov 17.
RNA and DNA play distinct roles in biological systems. However, the underlying physicochemical difference has been poorly understood, in particular, that in dynamical aspects. In this paper, we report on a comparative study of the formation-dissociation dynamics of a hairpin structure of RNA and DNA with development of two-color two-dimensional fluorescence lifetime correlation spectroscopy (two-color 2D FLCS). In this extension of 2D FLCS, we newly introduce the two-color detection scheme to analyze not only donor fluorescence photons but also acceptor fluorescence photons from a doubly labeled Förster resonance energy transfer (FRET) pair. This new 2D FLCS is utilized to resolve multiple species present in an equilibrated condition with a microsecond time resolution and enhanced sensitivity, and the combined use with the filtered fluorescence correlation spectroscopy (FCS) method enables a quantitative discussion on microsecond structural dynamics occurring in the equilibrium. This integrated approach is applied to FRET-labeled RNA/DNA oligonucleotides having analogous hairpin-forming sequences, and it was revealed that the hairpin dissociation rate of RNA is an order of magnitude slower than that of DNA while their hairpin-forming rates are comparable. This marked difference is attributable to the distinct duplex structure of RNA and DNA. The present study demonstrates that the integrated approach combining two-color 2D FLCS and filtered FCS has a high potential for quantifying microsecond kinetics at the single-molecule level, which allows us to experimentally construct a free energy landscape.
RNA和DNA在生物系统中发挥着不同的作用。然而,其潜在的物理化学差异,尤其是动力学方面的差异,一直未得到很好的理解。在本文中,我们报道了一项利用双色二维荧光寿命相关光谱技术(双色二维FLCS)对RNA和DNA发夹结构的形成-解离动力学进行的比较研究。在这种二维FLCS的扩展中,我们新引入了双色检测方案,不仅可以分析供体荧光光子,还可以分析来自双标记福斯特共振能量转移(FRET)对的受体荧光光子。这种新的二维FLCS用于以微秒级的时间分辨率和更高的灵敏度解析处于平衡状态的多种物种,并且与滤波荧光相关光谱(FCS)方法结合使用能够对平衡状态下发生的微秒级结构动力学进行定量讨论。这种综合方法应用于具有类似发夹形成序列的FRET标记的RNA/DNA寡核苷酸,结果表明RNA的发夹解离速率比DNA慢一个数量级,而它们的发夹形成速率相当。这种显著差异归因于RNA和DNA不同的双链结构。本研究表明,结合双色二维FLCS和滤波FCS的综合方法在单分子水平上定量微秒级动力学方面具有很大潜力,这使我们能够通过实验构建自由能景观。