Department of Chemistry, Duke University, Durham, North Carolina, USA.
Biophys J. 2010 Feb 17;98(4):733-40. doi: 10.1016/j.bpj.2009.11.004.
In the studies of force-induced conformational transitions of biomolecules, the large timescale difference from experiments presents the challenge of obtaining convergent sampling for molecular dynamics simulations. To circumvent this fundamental problem, an approach combining the replica-exchange method and umbrella sampling (REM-US) was developed to simulate mechanical stretching of biomolecules under equilibrium conditions. Equilibrium properties of conformational transitions can be obtained directly from simulations without further assumptions. To test the performance, we carried out REM-US simulations of atomic force microscope (AFM) stretching and relaxing measurements on the polysaccharide pustulan, a (1-->6)-beta-D-glucan, which undergoes well-characterized rotameric transitions in the backbone bonds. With significantly enhanced sampling convergence and efficiency, the REM-US approach closely reproduced the equilibrium force-extension curves measured in AFM experiments. Consistent with the reversibility in the AFM measurements, the new approach generated identical force-extension curves in both stretching and relaxing simulations-an outcome not reported in previous studies, proving that equilibrium conditions were achieved in the simulations. REM-US may provide a robust approach to modeling of mechanical stretching on polysaccharides and even nucleic acids.
在研究生物分子力诱导构象转变的过程中,实验与分子动力学模拟之间巨大的时间尺度差异带来了获取收敛采样的挑战。为了解决这个基本问题,我们开发了一种结合 replica-exchange 方法和伞形采样(REM-US)的方法,以在平衡条件下模拟生物分子的机械拉伸。可以直接从模拟中获得构象转变的平衡性质,而无需进一步假设。为了测试性能,我们对多糖普鲁兰(一种(1->6)-β-D-葡聚糖)进行了原子力显微镜(AFM)拉伸和弛豫测量的 REM-US 模拟,该多糖在主链键中经历了特征性的构象转变。通过显著提高的采样收敛性和效率,REM-US 方法紧密地再现了在 AFM 实验中测量的平衡力-伸长曲线。与 AFM 测量中的可逆性一致,新方法在拉伸和弛豫模拟中生成了相同的力-伸长曲线——这是以前研究中没有报道的结果,证明了在模拟中达到了平衡条件。REM-US 可能为多糖甚至核酸的机械拉伸建模提供一种稳健的方法。