水准点(测量)
网络拓扑
分子动力学
能量(信号处理)
计算机科学
软件
结合能
动能
统计物理学
生物系统
热力学积分
缩小
能量最小化
化学
配体(生物化学)
拓扑(电路)
紧密结合
算法
软件工具
计算化学
总能量
近似误差
相对标准差
药物发现
材料科学
实验数据
热力学
相关性
势能
还原(数学)
物理
分子
作者
Germano Heinzelmann,David J. Huggins,Michael K. Gilson
标识
DOI:10.1021/acs.jcim.5c02175
摘要
Absolute (ABFE) and relative (RBFE) binding free energy calculations with all-atom molecular dynamics (MD) can significantly reduce costs in the early stages of drug discovery. We introduce a new implementation of the Binding Affinity Tool (BAT.py) software, which adds RBFE calculations using separated topologies (SepTop) to the already established ABFE fully automated workflow. SepTop combines the advantages of ABFE and RBFE, being applicable to ligands that have very little or no similarity, while at the same time avoiding common challenges of ABFE calculations, such as occluded binding sites and problematic conformational changes of the receptor upon ligand binding. Three different thermodynamic paths for the relative calculations were implemented into the BAT software using the AMBER and OpenMM simulation engines, and here we test them on the BRD4(2) benchmark system. We discuss their correlation with ABFE, standard RBFE, and experimental results, and also their associated computational cost.
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