Institute for Integrated Radiation and Nuclear Science, Kyoto University, Kumatori, Sennan-gun, Osaka, 590-0494, Japan.
Sci Rep. 2022 Jun 15;12(1):9970. doi: 10.1038/s41598-022-13982-9.
Solving structural ensembles of flexible biomolecules is a challenging research area. Here, we propose a method to obtain possible structural ensembles of a biomolecule based on small-angle X-ray scattering (SAXS) and molecular dynamics simulations. Our idea is to clip a time series that matches a SAXS profile from a simulation trajectory. To examine its practicability, we applied our idea to a multi-domain protein ER-60 and successfully extracted time series longer than 1 micro second from trajectories of coarse-grained molecular dynamics simulations. In the extracted time series, the domain conformation was distributed continuously and smoothly in a conformational space. Preferred domain conformations were also observed. Diversity among scattering curves calculated from each ER-60 structure was interpreted to reflect an open-close motion of the protein. Although our approach did not provide a unique solution for the structural ensemble of the biomolecule, each extracted time series can be an element of the real behavior of ER-60. Considering its low computational cost, our approach will play a key role to identify biomolecular dynamics by integrating SAXS, simulations, and other experiments.
解决柔性生物分子的结构集合是一个具有挑战性的研究领域。在这里,我们提出了一种基于小角 X 射线散射(SAXS)和分子动力学模拟来获得生物分子可能的结构集合的方法。我们的想法是从模拟轨迹中剪辑与 SAXS 轮廓匹配的时间序列。为了检验其可行性,我们将我们的想法应用于多结构域蛋白 ER-60,并成功地从粗粒度分子动力学模拟轨迹中提取了超过 1 微秒的时间序列。在提取的时间序列中,结构域构象在构象空间中连续而平滑地分布。还观察到了首选的结构域构象。从每个 ER-60 结构计算出的散射曲线之间的多样性被解释为反映了蛋白质的开-合运动。尽管我们的方法没有为生物分子的结构集合提供独特的解决方案,但每个提取的时间序列都可以是 ER-60 实际行为的一个要素。考虑到其低计算成本,我们的方法将通过整合 SAXS、模拟和其他实验来识别生物分子动力学方面发挥关键作用。