Fraternali F, Van Gunsteren W F
Laboratoire de Modelisation et Simulations Moleculaires, Strasbourg, France.
J Mol Biol. 1996 Mar 15;256(5):939-48. doi: 10.1006/jmbi.1996.0139.
An empirical solvation model that allows for the elimination of solvent degrees of freedom in molecular dynamics (MD) simulations of biomolecules is proposed. The potential of mean force due to the first solvation shell is approximated by means of a simple, easily derivable analytic function of the solvent-accessible surface area of the molecule. The solvent contribution to the free energy is evaluated by means of only two atomic solvation parameters. This approach requires about 30% more computational effort than an in vacuo simulation, but a factor of 10 to 50 less than a MD simulation involving solvation by explicit water molecules. The implicit solvation model is assessed by application to proteins of different size. Average structural properties are calculated and compared to values obtained from X-ray structures and from MD simulations using explicit water molecules. The complementarity of the implicit solvation force and the intra-solute force field has been checked. The artefacts induced by the use of a vacuum boundary condition without solvation force in a MD simulation are considerably reduced.
提出了一种经验溶剂化模型,该模型可在生物分子的分子动力学(MD)模拟中消除溶剂自由度。由于第一溶剂化层产生的平均力势通过分子溶剂可及表面积的一个简单、易于推导的解析函数来近似。溶剂对自由能的贡献仅通过两个原子溶剂化参数来评估。这种方法比真空模拟所需的计算量大约多30%,但比涉及用显式水分子进行溶剂化的MD模拟少10到50倍。通过应用于不同大小的蛋白质来评估隐式溶剂化模型。计算平均结构性质,并与从X射线结构以及使用显式水分子的MD模拟获得的值进行比较。已检查隐式溶剂化力和溶质内力场的互补性。在MD模拟中使用无溶剂化力的真空边界条件所引起的假象显著减少。