Imamura Hideo, Chen Jeff Z Y
Department of Physics, University of Waterloo, Waterloo, Ontario, Canada.
Proteins. 2006 May 15;63(3):555-70. doi: 10.1002/prot.20846.
We study the dependence of folding time, nucleation site, and stability of a model beta-hairpin on the location of a cross-strand hydrophobic pair, using a coarse-grained off-lattice model with the aid of Monte Carlo simulations. Our simulations have produced 6500 independent folding trajectories dynamically, forming the basis for extensive statistical analysis. Four folding pathways, zipping-out, middle-out, zipping-in, and reptation, have been closely monitored and discussed in all seven sequences studied. A hydrophobic pair placed near the beta-turn or in the middle section effectively speed up folding; a hydrophobic pair placed close to the terminal ends or next to the beta-turn encourages stability of the entire chain.
我们借助蒙特卡罗模拟,使用粗粒度非晶格模型,研究了模型β-发夹的折叠时间、成核位点和稳定性对跨链疏水对位置的依赖性。我们的模拟动态生成了6500条独立的折叠轨迹,为广泛的统计分析奠定了基础。在所研究的所有七个序列中,对四种折叠途径,即拉链式向外、中间向外、拉链式向内和蛇行式,进行了密切监测和讨论。置于β-转角附近或中间部分的疏水对可有效加速折叠;靠近末端或β-转角旁边的疏水对有助于增强整个链的稳定性。