Optimization of Protein-Ligand Electrostatic Interactions Using an Alchemical Free-Energy Method.

ABSTRACT: We present an explicit solvent alchemical free-energy method for optimizing the partial charges of a ligand to maximize the binding affinity with a receptor. This methodology can be applied to known ligand-protein complexes to determine an optimized set of ligand partial atomic changes. Three protein-ligand complexes have been optimized in this work: FXa, P38, and the androgen receptor. The sets of optimized charges can be used to identify design principles for chemical changes to the ligands which improve the binding affinity for all three systems. In this work, beneficial chemical mutations are generated from these principles and the resulting molecules tested using free-energy perturbation calculations. We show that three quarters of our chemical changes are predicted to improve the bin

SUBMITTER: Wade AD 

PROVIDER: S-EPMC7007198 | biostudies-literature | 2019 Nov

REPOSITORIES: biostudies-literature