Chen Alan A, Draper David E, Pappu Rohit V
Molecular Biophysics Program and Center for Computational Biology, Washington University School of Medicine, St. Louis, MO 63130, USA.
J Mol Biol. 2009 Jul 24;390(4):805-19. doi: 10.1016/j.jmb.2009.05.071. Epub 2009 May 29.
A kissing loop is a highly stable complex formed by loop-loop base-pairing between two RNA hairpins. This common structural motif is utilized in a wide variety of RNA-mediated processes, including antisense recognition, substrate recognition in riboswitches, and viral replication. Recent work has shown that the Tar-Tar() complex, an archetypal kissing loop, can form without Mg(2+), so long as high concentrations of alkali chloride salts are present. Interestingly, the stability of the complex is found to decrease with increasing cation size. In this work, we used molecular simulations to develop a molecular-level understanding of the origins of the observed counterion specificity. The ionic atmosphere of the Tar-Tar() complex was examined in the presence of 800 mm (where m denotes molality) NaCl, KCl, or CsCl. We used spatial free-energy density profiles to analyze differences in counterion accumulation at different spatial extents from the RNA molecule. We found that the lowest free-energy levels, which are situated in the vicinity of the loop-loop interface, can accommodate roughly two counterions, irrespective of counterion type. However, as we moved into higher free-energy levels, which are farther from the loop-loop interface, we observed increased differences in the numbers of accumulated counterions, with this number being largest for Na(+) and smallest for Cs(+). We analyzed the source of these differences and were able to attribute these to two distinct features: The extent of partial dehydration varies based on cation type; the smaller the cation, the greater the degree of dehydration. While smaller ions bind their first-hydration-shell water molecules more tightly than larger ions, they are also able to shed these water molecules for stronger electrostatic interactions with the RNA molecule. Secondly, we observed a distinct asymmetry in the numbers of accumulated cations around each hairpin in the Tar-Tar() complex. We were able to ascribe this asymmetry to the presence of a guanine tract in the Tar hairpin, which facilitates partial dehydration of the counterions. However, the smaller ions compensate for this asymmetry by forming a belt around the loop-loop interface in intermediate free-energy levels. As a result, the degree of asymmetry in counterion accumulation around individual hairpins shows an inverse correlation with the experimentally observed cation specificity for the stability of Tar-Tar() (i.e., the smaller the asymmetry, the greater the experimentally observed stability). This in turn provides a plausible explanation for why the smaller cations help stabilize the Tar-Tar() complex better than the larger cations. These findings suggest that the specific sequence and structural features of the Tar-Tar() complex may be the source of the experimentally observed cation specificity in Tar-Tar(*) stability. Our results lead to testable predictions for how changes in sequence might alter the observed counterion specificity in kissing loop stability.
接吻环是由两个RNA发夹之间的环-环碱基配对形成的高度稳定的复合物。这种常见的结构基序被用于多种RNA介导的过程,包括反义识别、核糖开关中的底物识别和病毒复制。最近的研究表明,典型的接吻环Tar-Tar()复合物,只要存在高浓度的碱金属氯化物盐,就可以在没有Mg(2+)的情况下形成。有趣的是,发现该复合物的稳定性随着阳离子尺寸的增加而降低。在这项工作中,我们使用分子模拟从分子水平上理解观察到的抗衡离子特异性的起源。在800 mmol/kg(其中m表示质量摩尔浓度)的NaCl、KCl或CsCl存在下,研究了Tar-Tar()复合物的离子氛围。我们使用空间自由能密度分布来分析在距RNA分子不同空间范围内抗衡离子积累的差异。我们发现,位于环-环界面附近的最低自由能水平可以容纳大约两个抗衡离子,与抗衡离子类型无关。然而,当我们进入离环-环界面更远的更高自由能水平时,我们观察到积累的抗衡离子数量的差异增加,其中Na(+)的数量最多,Cs(+)的数量最少。我们分析了这些差异的来源,并将其归因于两个不同的特征:部分脱水的程度因阳离子类型而异;阳离子越小,脱水程度越大。虽然较小的离子比较大的离子更紧密地结合其第一水合层水分子,但它们也能够脱去这些水分子,以便与RNA分子进行更强的静电相互作用。其次,我们在Tar-Tar()复合物中观察到每个发夹周围积累的阳离子数量存在明显的不对称性。我们将这种不对称性归因于Tar发夹中鸟嘌呤序列的存在,它促进了抗衡离子的部分脱水。然而,较小的离子通过在中间自由能水平的环-环界面周围形成一条带,来补偿这种不对称性。结果,单个发夹周围抗衡离子积累的不对称程度与实验观察到的Tar-Tar()稳定性的阳离子特异性呈负相关(即不对称性越小,实验观察到的稳定性越大)。这反过来又为较小的阳离子比较大的阳离子更好地稳定Tar-Tar()复合物提供了一个合理的解释。这些发现表明,Tar-Tar()复合物的特定序列和结构特征可能是实验观察到的Tar-Tar(*)稳定性中阳离子特异性的来源。我们的结果为序列变化如何改变接吻环稳定性中观察到的抗衡离子特异性提供了可检验的预测。