Importance of accurate charges in molecular docking: Quantum mechanical/molecular mechanical (QM/MM) approach

Abstract

The extent to which accuracy of electric charges plays a role in protein‐ligand docking is investigated through development of a docking algorithm, which incorporates quantum mechanical/molecular mechanical (QM/MM) calculations. In this algorithm, fixed charges of ligands obtained from force field parameterization are replaced by QM/MM calculations in the protein environment, treating only the ligands as the quantum region. The algorithm is tested on a set of 40 cocrystallized structures taken from the Protein Data Bank (PDB) and provides strong evidence that use of nonfixed charges is important. An algorithm, dubbed “Survival of the Fittest” (SOF) algorithm, is implemented to incorporate QM/MM charge calculations without any prior knowledge of native structures of the complexes. Using an iterative protocol, this algorithm is able in many cases to converge to a nativelike structure in systems where redocking of the ligand using a standard fixed charge force field exhibits nontrivial errors. The results demonstrate that polarization effects can play a significant role in determining the structures of protein‐ligand complexes, and provide a promising start towards the development of more accurate docking methods for lead optimization applications. © 2005 Wiley Periodicals, Inc. J Comput Chem 26: 915–931, 2005