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Molecular modeling study of checkpoint kinase 1 inhibitors by multiple docking strategies and prime/MM–GBSA calculation
Author(s) -
Du Juan,
Sun Huijun,
Xi Lili,
Li Jiazhong,
Yang Ying,
Liu Huanxiang,
Yao Xiaojun
Publication year - 2011
Publication title -
journal of computational chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.907
H-Index - 188
eISSN - 1096-987X
pISSN - 0192-8651
DOI - 10.1002/jcc.21859
Subject(s) - docking (animal) , molecular mechanics , chemistry , protein–ligand docking , computational biology , molecular dynamics , computational chemistry , virtual screening , biology , medicine , nursing
Developing chemicals that inhibit checkpoint kinase 1 (Chk1) is a promising adjuvant therapeutic to improve the efficacy and selectivity of DNA‐targeting agents. Reliable prediction of binding‐free energy and binding affinity of Chk1 inhibitors can provide a guide for rational drug design. In this study, multiple docking strategies and Prime/Molecular Mechanics Generalized Born Surface Area (Prime/MM‐GBSA) calculation were applied to predict the binding mode and free energy for a series of benzoisoquinolinones as Chk1 inhibitors. Reliable docking results were obtained using induced‐fit docking and quantum mechanics/molecular mechanics (QM/MM) docking, which showed superior performance on both ligand binding pose and docking score accuracy to the rigid‐receptor docking. Then, the Prime/MM–GBSA method based on the docking complex was used to predict the binding‐free energy. The combined use of QM/MM docking and Prime/MM–GBSA method could give a high correlation between the predicted binding‐free energy and experimentally determined pIC 50 . The molecular docking combined with Prime/MM–GBSA simulation can not only be used to rapidly and accurately predict the binding‐free energy of novel Chk1 inhibitors but also provide a novel strategy for lead discovery and optimization targeting Chk1. © 2011 Wiley Periodicals, Inc. J Comput Chem, 2011