Using molecular docking and molecular dynamics to investigate protein-ligand interactions

被引:103
作者
Morris, Connor J. [1 ]
Della Corte, Dennis [1 ]
机构
[1] Brigham Young Univ, Dept Phys & Astron, Provo, UT 84602 USA
来源
MODERN PHYSICS LETTERS B | 2021年 / 35卷 / 08期
关键词
Molecular docking; molecular dynamics (MD); ensemble docking; consensus docking; blind docking; protein engineering; drug discovery; protein-ligand interactions; INDUCED FIT; BINDING; PREDICTION; OPTIMIZATION; SIMULATIONS; FLEXIBILITY; RELIABILITY; SELECTION; TOOLS;
D O I
10.1142/S0217984921300027
中图分类号
O59 [应用物理学];
学科分类号
摘要
Molecular docking and molecular dynamics (MD) are powerful tools used to investigate protein-ligand interactions. Molecular docking programs predict the binding pose and affinity of a protein-ligand complex, while MD can be used to incorporate flexibility into docking calculations and gain further information on the kinetics and stability of the protein-ligand bond. This review covers state-of-the-art methods of using molecular docking and MD to explore protein-ligand interactions, with emphasis on application to drug discovery. We also call for further research on combining common molecular docking and MD methods.
引用
收藏
页数:15
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