Department of Pharmaceutical Sciences, School of Pharmacy, University of Maryland, Baltimore, Maryland 21201, USA.
J Am Chem Soc. 2009 Dec 16;131(49):17759-61. doi: 10.1021/ja905795v.
Urea titration of RNA by urea is an effective approach to investigate the forces stabilizing this biologically important molecule. We used all atom molecular dynamics simulations using two urea force fields and two RNA constructs to elucidate in atomic detail the destabilization mechanism of folded RNA in aqueous urea solutions. Urea denatures RNA by forming multiple hydrogen bonds with the RNA bases and has little influence on the phosphodiester backbone. Most significantly we discovered that urea engages in stacking interactions with the bases. We also estimate, for the first time, the m-value for RNA, which is a measure of the strength of urea-RNA interactions. Our work provides a conceptual understanding of the mechanism by which urea enhances RNA folding rates.
尿素滴定 RNA 是一种研究稳定这种生物重要分子的力的有效方法。我们使用两种尿素力场和两种 RNA 结构,通过全原子分子动力学模拟,详细阐明了在水合尿素溶液中折叠 RNA 的失稳机制。尿素通过与 RNA 碱基形成多个氢键来使 RNA 变性,并且对磷酸二酯骨架几乎没有影响。最重要的是,我们发现尿素与碱基发生堆积相互作用。我们还首次估计了 RNA 的 m 值,这是衡量尿素与 RNA 相互作用强度的指标。我们的工作提供了对尿素增强 RNA 折叠速率的机制的概念理解。