Université de Lyon, Université Lyon 1, Villeurbanne, 69622, France.
J Am Soc Mass Spectrom. 2012 Jul;23(7):1279-88. doi: 10.1007/s13361-012-0391-1. Epub 2012 May 10.
Following a recent effort [J. Am. Soc. Mass Spectrom. 23, 386-396 (2012)], we continue to explore computational methodologies for generating molecular conformations to support collisional cross sections suggested by ion mobility measurements. Here, adaptively biased molecular dynamics (ABMD) simulations are used to sample the configuration space and to achieve flat-histogram sampling along the reaction coordinates of the first two moments of the gyration tensor. The method is tested and compared with replica-exchange simulations on triply-protonated bradykinin and on a larger 25-residue peptide. It is found to have a much higher efficiency for producing large sets of conformations in a broad range of diffusion cross-sections, whereas it does not compete with conventional replica-exchange molecular dynamics in locating the lowest-energy structure. Nevertheless, the broad sampling obtained from the ABMD method allows to quantitatively correlate the diffusion cross-section Ω with other geometric order parameters that have simpler interpretation. The strong correlations found between the diffusion cross-section and the radius of gyration, the surface area and the volume of the convex hull suggest an optimal template for accurately mimicking the variations of Ω in a broad range of conformations, using only geometrical information and doing so at a very moderate computational cost. The existence of such a correlation is confirmed on the much larger protein α-lactalbumin.
在最近的努力之后[J. Am. Soc. Mass Spectrom. 23, 386-396 (2012)],我们继续探索用于生成分子构象的计算方法,以支持离子淌度测量所建议的碰撞截面。在这里,自适应偏置分子动力学 (ABMD) 模拟用于采样构象空间,并沿着旋轮张量的前两个矩的反应坐标实现直方图的平坦采样。该方法在三重质子化缓激肽和更大的 25 残基肽上进行了测试和与 replica-exchange 模拟的比较。结果表明,该方法在产生大范围扩散截面的大量构象方面具有更高的效率,而在定位最低能量结构方面并不与传统的 replica-exchange 分子动力学竞争。然而,ABMD 方法获得的广泛采样允许定量关联扩散截面Ω与其他具有更简单解释的几何有序参数。发现扩散截面与回转半径、表面积和凸包体积之间存在很强的相关性,这表明使用仅几何信息并以非常适中的计算成本在广泛构象范围内准确模拟Ω变化的最佳模板。这种相关性在更大的蛋白质α-乳白蛋白上得到了证实。