Kognole Abhishek A, MacKerell Alexander D
Department of Pharmaceutical Sciences, School of Pharmacy, University of Maryland, Baltimore, Maryland.
Department of Pharmaceutical Sciences, School of Pharmacy, University of Maryland, Baltimore, Maryland.
Biophys J. 2020 Mar 24;118(6):1424-1437. doi: 10.1016/j.bpj.2020.01.021. Epub 2020 Jan 28.
RNA molecules perform a variety of biological functions for which the correct three-dimensional structure is essential, including as ribozymes where they catalyze chemical reactions. Metal ions, especially Mg, neutralize these negatively charged nucleic acids and specifically stabilize RNA tertiary structures as well as impact the folding landscape of RNAs as they assume their tertiary structures. Specific binding sites of Mg in folded conformations of RNA have been studied extensively; however, the full range of interactions of the ion with compact intermediates and unfolded states of RNA is challenging to investigate, and the atomic details of the mechanism by which the ion facilitates tertiary structure formation is not fully known. Here, umbrella sampling combined with oscillating chemical potential Grand Canonical Monte Carlo/molecular dynamics simulations are used to capture the energetics and atomic-level details of Mg-RNA interactions that occur along an unfolding pathway of the Twister ribozyme. The free energy profiles reveal stabilization of partially unfolded states by Mg, as observed in unfolding experiments, with this stabilization being due to increased sampling of simultaneous interactions of Mg with two or more nonsequential phosphate groups. Notably, these results indicate a push-pull mechanism in which the Mg-RNA interactions actually lead to destabilization of specific nonsequential phosphate-phosphate interactions (i.e., pushed apart), whereas other interactions are stabilized (i.e., pulled together), a balance that stabilizes unfolded states and facilitates the folding of Twister, including the formation of hydrogen bonds associated with the tertiary structure. This study establishes a better understanding of how Mg-ion interactions contribute to RNA structural properties and stability.
RNA分子执行多种生物学功能,而正确的三维结构对这些功能至关重要,包括作为核酶催化化学反应。金属离子,尤其是镁离子,中和这些带负电荷的核酸,特异性地稳定RNA三级结构,并在RNA形成三级结构时影响其折叠态势。RNA折叠构象中镁离子的特异性结合位点已得到广泛研究;然而,研究离子与RNA紧密中间体和未折叠状态的全部相互作用具有挑战性,且离子促进三级结构形成机制的原子细节尚不完全清楚。在此,采用伞形采样结合振荡化学势巨正则蒙特卡罗/分子动力学模拟,以捕捉沿着Twister核酶解折叠途径发生的镁离子与RNA相互作用的能量学和原子水平细节。自由能分布揭示了镁离子对部分解折叠状态的稳定作用,这与解折叠实验中观察到的一致,这种稳定作用是由于镁离子与两个或更多非连续磷酸基团同时相互作用的采样增加所致。值得注意的是,这些结果表明了一种推拉机制,其中镁离子与RNA的相互作用实际上导致特定非连续磷酸-磷酸相互作用的不稳定(即推开),而其他相互作用则得到稳定(即拉近),这种平衡稳定了解折叠状态并促进Twister的折叠,包括与三级结构相关的氢键形成。这项研究有助于更好地理解镁离子相互作用如何影响RNA的结构特性和稳定性。