Di Palma Francesco, Bottaro Sandro, Bussi Giovanni
BMC Bioinformatics. 2015;16 Suppl 9(Suppl 9):S6. doi: 10.1186/1471-2105-16-S9-S6. Epub 2015 Jun 1.
Riboswitches are cis-acting regulatory RNA elements prevalently located in the leader sequences of bacterial mRNA. An adenine sensing riboswitch cis-regulates adeninosine deaminase gene (add) in Vibrio vulnificus. The structural mechanism regulating its conformational changes upon ligand binding mostly remains to be elucidated. In this open framework it has been suggested that the ligand stabilizes the interaction of the distal "kissing loop" complex. Using accurate full-atom molecular dynamics with explicit solvent in combination with enhanced sampling techniques and advanced analysis methods it could be possible to provide a more detailed perspective on the formation of these tertiary contacts.
In this work, we used umbrella sampling simulations to study the thermodynamics of the kissing loop complex in the presence and in the absence of the cognate ligand. We enforced the breaking/formation of the loop-loop interaction restraining the distance between the two loops. We also assessed the convergence of the results by using two alternative initialization protocols. A structural analysis was performed using a novel approach to analyze base contacts.
Contacts between the two loops were progressively lost when larger inter-loop distances were enforced. Inter-loop Watson-Crick contacts survived at larger separation when compared with non-canonical pairing and stacking interactions. Intra-loop stacking contacts remained formed upon loop undocking. Our simulations qualitatively indicated that the ligand could stabilize the kissing loop complex. We also compared with previously published simulation studies.
Kissing complex stabilization given by the ligand was compatible with available experimental data. However, the dependence of its value on the initialization protocol of the umbrella sampling simulations posed some questions on the quantitative interpretation of the results and called for better converged enhanced sampling simulations.
核糖开关是顺式作用的调节RNA元件,普遍存在于细菌mRNA的前导序列中。一种腺嘌呤感应核糖开关可顺式调节创伤弧菌中的腺苷脱氨酶基因(add)。其在配体结合后调节构象变化的结构机制大多仍有待阐明。在这个开放框架中,有人提出配体可稳定远端“亲吻环”复合物的相互作用。结合明确的溶剂,使用精确的全原子分子动力学,再结合增强采样技术和先进分析方法,有可能为这些三级接触的形成提供更详细的视角。
在这项工作中,我们使用伞形采样模拟来研究在有和没有同源配体的情况下亲吻环复合物的热力学。我们强制环-环相互作用的断裂/形成,限制两个环之间的距离。我们还通过使用两种替代初始化协议评估了结果的收敛性。使用一种新颖的方法对碱基接触进行了结构分析。
当强制拉大环间距离时,两个环之间的接触逐渐丧失。与非经典配对和堆积相互作用相比,环间沃森-克里克接触在更大的间距下仍能保留。环解链时,环内堆积接触仍保持形成。我们的模拟定性地表明配体可稳定亲吻环复合物。我们还与之前发表的模拟研究进行了比较。
配体赋予的亲吻复合物稳定性与现有实验数据相符。然而,其值对伞形采样模拟初始化协议的依赖性对结果的定量解释提出了一些问题,需要更好收敛的增强采样模拟。