JILA, University of Colorado and National Institute of Standards and Technology, and Department of Chemistry and Biochemistry, University of Colorado, Boulder, Colorado 80309-0440, USA.
Biochemistry. 2012 May 8;51(18):3732-43. doi: 10.1021/bi201420a. Epub 2012 Apr 23.
Cations have long been associated with formation of native RNA structure and are commonly thought to stabilize the formation of tertiary contacts by favorably interacting with the electrostatic potential of the RNA, giving rise to an "ion atmosphere". A significant amount of information regarding the thermodynamics of structural transitions in the presence of an ion atmosphere has accumulated and suggests stabilization is dominated by entropic terms. This work provides an analysis of how RNA-cation interactions affect the entropy and enthalpy associated with an RNA tertiary transition. Specifically, temperature-dependent single-molecule fluorescence resonance energy transfer studies have been exploited to determine the free energy (ΔG°), enthalpy (ΔH°), and entropy (ΔS°) of folding for an isolated tetraloop-receptor tertiary interaction as a function of Na(+) concentration. Somewhat unexpectedly, increasing the Na(+) concentration changes the folding enthalpy from a strongly exothermic process [e.g., ΔH° = -26(2) kcal/mol at 180 mM] to a weakly exothermic process [e.g., ΔH° = -4(1) kcal/mol at 630 mM]. As a direct corollary, it is the strong increase in folding entropy [Δ(ΔS°) > 0] that compensates for this loss of exothermicity for the achievement of more favorable folding [Δ(ΔG°) < 0] at higher Na(+) concentrations. In conjunction with corresponding measurements of the thermodynamics of the transition state barrier, these data provide a detailed description of the folding pathway associated with the GAAA tetraloop-receptor interaction as a function of Na(+) concentration. The results support a potentially universal mechanism for monovalent facilitated RNA folding, whereby an increasing monovalent concentration stabilizes tertiary structure by reducing the entropic penalty for folding.
阳离子长期以来一直与天然 RNA 结构的形成有关,通常被认为通过与 RNA 的静电势能有利地相互作用来稳定三级接触的形成,从而产生“离子气氛”。已经积累了大量关于离子气氛存在下结构转变热力学的信息,这些信息表明稳定作用主要由熵项决定。这项工作分析了 RNA-阳离子相互作用如何影响与 RNA 三级转变相关的熵和焓。具体来说,利用温度依赖性单分子荧光共振能量转移研究来确定作为 Na(+)浓度函数的孤立四螺旋受体三级相互作用的折叠自由能 (ΔG°)、焓 (ΔH°) 和熵 (ΔS°)。出人意料的是,增加 Na(+)浓度会使折叠焓从强放热过程[例如,在 180 mM 时 ΔH°=-26(2)kcal/mol]变为弱放热过程[例如,在 630 mM 时 ΔH°=-4(1)kcal/mol]。作为直接推论,是折叠熵的强烈增加[Δ(ΔS°)>0]弥补了这种放热损失,从而在更高的 Na(+)浓度下实现了更有利的折叠[Δ(ΔG°)<0]。结合对过渡态势垒热力学的相应测量,这些数据提供了 GAAA 四螺旋受体相互作用折叠途径与 Na(+)浓度关系的详细描述。结果支持了单价促进 RNA 折叠的潜在通用机制,其中单价浓度的增加通过降低折叠的熵罚来稳定三级结构。