School of Life Sciences, Jilin University, Changchun, 130012 China.
MOE Key Laboratory of Molecular Enzymology and Engineering, Jilin University, Changchun, 130012 China.
Sci Rep. 2016 Oct 6;6:34481. doi: 10.1038/srep34481.
Protein allostery requires dynamical structural correlations. Physical origin of which, however, remain elusive despite intensive studies during last two and half decades. Based on analysis of molecular dynamics (MD) simulation trajectories for ten proteins with different sizes and folds, we found that nonlinear backbone torsional pair (BTP) correlations, which are mainly spatially long-ranged and are dominantly executed by loop residues, exist extensively in most analyzed proteins. Examination of torsional motion for correlated BTPs suggested that such nonlinear correlations are mainly associated aharmonic torsional state transitions and in some cases strongly anisotropic local torsional motion of participating torsions, and occur on widely different and relatively longer time scales. In contrast, correlations between backbone torsions in stable α helices and β strands are mainly linear and spatially short-ranged, and are more likely to associate with harmonic local torsional motion. Further analysis revealed that the direct cause of nonlinear contributions are heterogeneous linear correlations. These findings implicate a general search strategy for novel allosteric modulation sites of protein activities.
蛋白质变构需要动态结构相关性。尽管在过去的二十五年中进行了深入的研究,但这种相关性的物理起源仍然难以捉摸。基于对十个具有不同大小和折叠的蛋白质的分子动力学(MD)模拟轨迹的分析,我们发现非线性骨架扭转对(BTP)相关性广泛存在于大多数分析的蛋白质中。这些相关性主要是空间上远程的,主要由环残基执行。对相关 BTP 的扭转运动的研究表明,这种非线性相关性主要与非谐扭转态跃迁有关,在某些情况下与参与扭转的强各向异性局部扭转运动有关,而且发生在广泛不同且相对较长的时间尺度上。相比之下,稳定的α螺旋和β折叠中骨架扭转之间的相关性主要是线性的和空间短程的,并且更可能与谐局部扭转运动相关。进一步的分析表明,非线性贡献的直接原因是不均匀的线性相关性。这些发现暗示了一种寻找蛋白质活性新型变构调节位点的一般搜索策略。