Lenz Peter, Zagrovic Bojan, Shapiro Jessica, Pande Vijay S
Lyman Laboratory of Physics, Harvard University, Cambridge, Massachusetts 02138, USA.
J Chem Phys. 2004 Apr 8;120(14):6769-78. doi: 10.1063/1.1667470.
The theoretical concept of folding probability, p(fold), has proven to be a useful means to characterize the kinetics of protein folding. Here, we illustrate the practical importance of p(fold) and demonstrate how it can be determined theoretically. We derive a general analytical expression for p(fold) and show how it can be estimated from simulations for systems where the transition rates between the relevant microstates are not known. By analyzing the Ising model we are able to determine the scaling behavior of the numerical error in the p(fold) estimate as function of the number of analyzed Monte Carlo runs. We apply our method to a simple, newly developed protein folding model for the formation of alpha helices. It is demonstrated that our technique highly parallelizes the calculation of p(fold) and that it is orders of magnitude more efficient than conventional approaches.
折叠概率p(fold)的理论概念已被证明是表征蛋白质折叠动力学的一种有用方法。在此,我们阐述了p(fold)的实际重要性,并演示了如何从理论上确定它。我们推导了p(fold)的一般解析表达式,并展示了如何从相关微观状态之间的跃迁速率未知的系统的模拟中估计它。通过分析伊辛模型,我们能够确定p(fold)估计值中数值误差随分析的蒙特卡罗运行次数的缩放行为。我们将我们的方法应用于一个新开发的用于形成α螺旋的简单蛋白质折叠模型。结果表明,我们的技术使p(fold)的计算高度并行化,并且比传统方法效率高几个数量级。