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定义和测试 GROMOS 力场版本 54A7 和 54B7。

Definition and testing of the GROMOS force-field versions 54A7 and 54B7.

机构信息

Laboratory of Physical Chemistry, Swiss Federal Institute of Technology ETH, Zürich, Switzerland.

出版信息

Eur Biophys J. 2011 Jul;40(7):843-56. doi: 10.1007/s00249-011-0700-9. Epub 2011 Apr 30.

Abstract

New parameter sets of the GROMOS biomolecular force field, 54A7 and 54B7, are introduced. These parameter sets summarise some previously published force field modifications: The 53A6 helical propensities are corrected through new φ/ψ torsional angle terms and a modification of the N-H, C=O repulsion, a new atom type for a charged -CH(3) in the choline moiety is added, the Na(+) and Cl(-) ions are modified to reproduce the free energy of hydration, and additional improper torsional angle types for free energy calculations involving a chirality change are introduced. The new helical propensity modification is tested using the benchmark proteins hen egg-white lysozyme, fox1 RNA binding domain, chorismate mutase and the GCN4-p1 peptide. The stability of the proteins is improved in comparison with the 53A6 force field, and good agreement with a range of primary experimental data is obtained.

摘要

介绍了 GROMOS 生物分子力场的新参数集,54A7 和 54B7。这些参数集总结了一些以前发表的力场修正:通过新的φ/ψ扭转角项和 N-H、C=O 斥力的修正,对 53A6 螺旋倾向进行了修正,在胆碱部分添加了带电荷的-CH(3)的新原子类型,对 Na(+)和 Cl(-)离子进行了修正,以重现水合自由能,并且引入了用于涉及手性变化的自由能计算的其他不合适的扭转角类型。使用基准蛋白鸡卵清溶菌酶、fox1 RNA 结合域、色氨酸合酶和 GCN4-p1 肽测试了新的螺旋倾向修正。与 53A6 力场相比,蛋白质的稳定性得到了提高,并与一系列原始实验数据得到了很好的一致性。

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