Mark A E, van Gunsteren W F
Department of Physical Chemistry, Swiss Federal Institute of Technology, ETH Zentrum, Zuerich.
J Mol Biol. 1994 Jul 8;240(2):167-76. doi: 10.1006/jmbi.1994.1430.
Recently, a number of methods have been proposed that are designed to extract contributions to the change in free energy associated with a given perturbation or mutation of a protein originating from specific residue-residue or atom-atom interactions, both based on theoretical calculations and on experimental data. We caution here that detailed analysis based on these methods is unreliable. It is demonstrated, both from first principles using statistical mechanics and by way of example, that in a general case a meaningful decomposition of the free energy in terms of specific residue-residue or atom-atom interactions is not possible.
最近,人们提出了许多方法,这些方法旨在基于理论计算和实验数据,提取与蛋白质特定残基-残基或原子-原子相互作用所导致的给定扰动或突变相关的自由能变化的贡献。我们在此提醒,基于这些方法的详细分析是不可靠的。从统计力学的第一原理以及通过实例都可以证明,在一般情况下,不可能根据特定的残基-残基或原子-原子相互作用对自由能进行有意义的分解。