化学
分子动力学
膜
溶解度
化学物理
扩散
分子扩散
力场(虚构)
统计物理学
水模型
热力学
计算化学
物理化学
物理
量子力学
生物化学
经济
公制(单位)
运营管理
作者
Richard M. Venable,Andreas Krämer,Richard W. Pastor
出处
期刊:Chemical Reviews
[American Chemical Society]
日期:2019-02-12
卷期号:119 (9): 5954-5997
被引量:313
标识
DOI:10.1021/acs.chemrev.8b00486
摘要
This Review illustrates the evaluation of permeability of lipid membranes from molecular dynamics (MD) simulation primarily using water and oxygen as examples. Membrane entrance, translocation, and exit of these simple permeants (one hydrophilic and one hydrophobic) can be simulated by conventional MD, and permeabilities can be evaluated directly by Fick's First Law, transition rates, and a global Bayesian analysis of the inhomogeneous solubility-diffusion model. The assorted results, many of which are applicable to simulations of nonbiological membranes, highlight the limitations of the homogeneous solubility diffusion model; support the utility of inhomogeneous solubility diffusion and compartmental models; underscore the need for comparison with experiment for both simple solvent systems (such as water/hexadecane) and well-characterized membranes; and demonstrate the need for microsecond simulations for even simple permeants like water and oxygen. Undulations, subdiffusion, fractional viscosity dependence, periodic boundary conditions, and recent developments in the field are also discussed. Last, while enhanced sampling methods and increasingly sophisticated treatments of diffusion add substantially to the repertoire of simulation-based approaches, they do not address directly the critical need for force fields with polarizability and multipoles, and constant pH methods.
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