Hoppe Travis, Minton Allen P
Laboratory of Chemical Physics and ‡Laboratory of Biochemistry and Genetics, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, United States Public Health Service , Bethesda, Maryland 20892, United States.
J Phys Chem B. 2016 Nov 23;120(46):11866-11872. doi: 10.1021/acs.jpcb.6b07736. Epub 2016 Nov 15.
In order to better understand how nonspecific interactions between solutes can modulate specific biochemical reactions taking place in complex media, we introduce a simplified model aimed at elucidating general principles. In this model, solutions containing two or three species of interacting globular proteins are modeled as a fluid of spherical particles interacting through square well potentials that qualitatively capture both steric hard core repulsion and longer-ranged attraction or repulsion. The excess chemical potential, or free energy of solvation, of each particle species is calculated as a function of species concentrations, particle radii, and square well interaction range and depth. The results of analytical models incorporating two-body and three-body interactions are compared with the estimates of free energy obtained via Widom insertion into simulated equilibrium square-well fluids. The analytical models agree well with results of numeric simulations carried out for a variety of model parameters and fluid compositions up to a total particle volume fraction of ca. 0.2.
为了更好地理解溶质之间的非特异性相互作用如何调节复杂介质中发生的特定生化反应,我们引入了一个简化模型,旨在阐明一般原理。在这个模型中,包含两种或三种相互作用的球状蛋白质的溶液被建模为通过方阱势相互作用的球形颗粒流体,该势定性地捕捉了空间硬核排斥以及更长程的吸引或排斥。计算每种颗粒物种的过量化学势或溶剂化自由能,作为物种浓度、颗粒半径以及方阱相互作用范围和深度的函数。将包含两体和三体相互作用的解析模型结果与通过维杜姆插入模拟平衡方阱流体获得的自由能估计值进行比较。对于各种模型参数和流体组成,直至总颗粒体积分数约为0.2,解析模型与数值模拟结果吻合良好。