Smith L J, Mark A E, Dobson C M, van Gunsteren W F
Oxford Centre for Molecular Sciences, University of Oxford, England.
Biochemistry. 1995 Aug 29;34(34):10918-31. doi: 10.1021/bi00034a026.
Three 1000 ps molecular dynamics simulations of hen lysozyme have been compared with a range of experimental NMR parameters in order to gain insight into the dynamical properties of the protein and to assess the significance of the motional events observed in the simulations. The simulations, one in vacuum and two in water, were used to estimate interproton distances (for comparison with NOE data), 3JHN alpha and 3J alpha beta coupling constants and 1H-15N order parameters. Comparison of these values with experimental data, particularly NOEs, enabled force field-induced changes to the structure during the simulations to be recognized. It has been shown, however, that these changes can be largely eliminated by slight modifications to the force field. Using a simulation performed in water with this modified force field, it has been found that 1H-15N order parameters calculated for side chain groups in particular correlate well with experimental values and reflect the substantial dependence of these motional properties on the environment, particularly surface exposure, in which the side chain is found. In this case, the simulation then provides models for the motional processes giving rise to the observed experimental data. The results indicate that the order parameter values reflect primarily the number of torsion angles about which rotameric interchange occurs. In addition to local motions, the two different domains of lysozyme have been found to behave differently in the simulations. Possible implications of these differences for the interpretation of unfolding simulations and experimental observations of folding intermediates for lysozyme are discussed.
对溶菌酶进行了三次1000皮秒的分子动力学模拟,并与一系列实验核磁共振参数进行了比较,以便深入了解该蛋白质的动力学特性,并评估模拟中观察到的运动事件的重要性。这三次模拟,一次在真空中进行,两次在水中进行,用于估算质子间距离(以便与核Overhauser效应(NOE)数据进行比较)、3JHNα和3Jαβ耦合常数以及1H-15N序参数。将这些值与实验数据,特别是NOE数据进行比较,能够识别模拟过程中力场引起的结构变化。然而,已经表明,通过对力场进行微小修改,这些变化在很大程度上可以消除。使用在水中用这种修改后的力场进行的模拟,发现特别是为侧链基团计算的1H-15N序参数与实验值相关性良好,并反映了这些运动特性对环境,特别是侧链所处表面暴露情况的强烈依赖性。在这种情况下,模拟随后为产生观察到的实验数据的运动过程提供了模型。结果表明,序参数值主要反映了发生旋转异构体互换的扭转角的数量。除了局部运动外,还发现在模拟中溶菌酶的两个不同结构域表现不同。讨论了这些差异对溶菌酶展开模拟和折叠中间体实验观察结果解释的可能影响。