Tirado-Rives J, Orozco M, Jorgensen W L
Department of Chemistry, Yale University, New Haven, Connecticut 06520-8107, USA.
Biochemistry. 1997 Jun 17;36(24):7313-29. doi: 10.1021/bi970096i.
Molecular dynamics simulations of barnase have been conducted both in water and in 8 M urea solution for 500 ps at 25 degrees C and for 2000 ps at 85 degrees C. The final structure of the aqueous simulation at room temperature matches closely the structure obtained by NMR and the experimentally observed protections from isotopic exchange. The comparison of the structures generated by the aqueous simulation at 85 degrees C reveals a trajectory composed of groups of geometrically related structures separated by narrow regions of rapid change in structure. The first of these regions displays changes in backbone rmsd to the crystal structure and solvent-accessible area suggestive of a transition state, while the properties observed during the final 300 ps of the simulation are consistent with a stable intermediate. These assignments were confirmed by calculation of the "progress along the reaction coordinate" phi-values using an empirical equation based on a linear response method. The pathway of unfolding defined in this fashion agrees well with the experimental results of site-directed mutagenesis in terms of secondary structure content of the transition state and the intermediate and reproduces the relative stability of the different elements of secondary structure. The results of the simulations in urea suggest a mechanism at the molecular level for its well-known enhancement of the denaturation of proteins. The analysis of radial distribution functions shows that the first solvation shell of the protein is enriched in urea relative to the bulk solvent. The displacement of water molecules allows greater exposure of hydrophobic side chains, as witnessed particularly in the analysis of solvent-accessible surface areas at the higher temperature. Almost all urea molecules in the first shell form at least one hydrogen bond with the protein. They provide a more favorable environment for accommodation of the remaining water molecules, and they facilitate the separation of secondary structure elements by acting as a bridge between groups previously forming intraprotein hydrogen bonds.
已在25摄氏度下于水中和8 M尿素溶液中对巴纳酶进行了500皮秒的分子动力学模拟,并在85摄氏度下进行了2000皮秒的模拟。室温下水相模拟的最终结构与通过核磁共振获得的结构以及实验观察到的同位素交换保护情况紧密匹配。85摄氏度下水相模拟生成的结构比较显示,其轨迹由几何相关结构组组成,这些结构组由结构快速变化的狭窄区域分隔开。这些区域中的第一个显示出与晶体结构的主链均方根偏差和溶剂可及面积的变化,暗示着一个过渡态,而在模拟的最后300皮秒期间观察到的性质与一个稳定中间体一致。通过使用基于线性响应方法的经验方程计算“沿反应坐标的进程”φ值,证实了这些归属。以这种方式定义的解折叠途径在过渡态和中间体的二级结构含量方面与定点诱变的实验结果非常吻合,并再现了二级结构不同元素的相对稳定性。尿素中的模拟结果表明了其众所周知的增强蛋白质变性作用在分子水平上的机制。径向分布函数分析表明,相对于本体溶剂,蛋白质的第一溶剂化层富含尿素。水分子的位移使疏水侧链有更大的暴露,这在较高温度下对溶剂可及表面积的分析中尤为明显。第一壳层中几乎所有的尿素分子都与蛋白质形成至少一个氢键。它们为容纳其余水分子提供了更有利的环境,并且通过充当先前形成蛋白质内氢键的基团之间的桥梁,促进了二级结构元件的分离。