Maragakis Paul, Spichty Martin, Karplus Martin
Department of Chemistry & Chemical Biology, Harvard University, Cambridge, MA 02138, USA.
J Phys Chem B. 2008 May 15;112(19):6168-74. doi: 10.1021/jp077037r. Epub 2008 Mar 11.
We derive a nonequilibrium thermodynamics identity (the "differential fluctuation theorem") that connects forward and reverse joint probabilities of nonequilibrium work and of arbitrary generalized coordinates corresponding to states of interest. This identity allows us to estimate the free energy difference between domains of these states. Our results follow from a general symmetry relation between averages over nonequilibrium forward and backward path functions derived by Crooks [Crooks, G. E. Phys. Rev. E 2000, 61, 2361-2366]. We show how several existing nonequilibrium thermodynamic identities can be obtained directly from the differential fluctuation theorem. We devise an approach for measuring conformational free energy differences, and we demonstrate its applicability to the analysis of molecular dynamics simulations by estimating the free energy difference between two conformers of the alanine dipeptide model system. We anticipate that these developments can be applied to the analysis of laboratory experiments.
我们推导了一个非平衡热力学恒等式(“微分涨落定理”),该恒等式将非平衡功以及与感兴趣状态相对应的任意广义坐标的正向和反向联合概率联系起来。这个恒等式使我们能够估计这些状态区域之间的自由能差。我们的结果源于克鲁克斯[Crooks, G. E. Phys. Rev. E 2000, 61, 2361 - 2366]推导的非平衡正向和反向路径函数平均值之间的一般对称关系。我们展示了如何直接从微分涨落定理获得几个现有的非平衡热力学恒等式。我们设计了一种测量构象自由能差的方法,并通过估计丙氨酸二肽模型系统两个构象之间的自由能差,证明了其在分子动力学模拟分析中的适用性。我们预计这些进展可应用于实验室实验的分析。