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- W1958906090 abstract "Force field accuracy is still one of the stalemates in biomolecular modeling. Model systems with high quality experimental data are valuable instruments for the validation and improvement of effective potentials. With respect to protein-ligand binding, organic host-guest complexes have long served as models for both experimental and computational studies because of the abundance of binding affinity data available for such systems. Binding affinity data collected for cyclodextrin (CD) inclusion complexes, a popular model for molecular recognition, is potentially a more reliable resource for tuning energy parameters than hydration free energy measurements. Convergence of binding free energy calculations on CD host-guest systems can also be obtained rapidly, thus offering the opportunity to assess the robustness of these parameters. In this work, we demonstrate how implicit solvent parameters can be developed using binding affinity experimental data and the binding energy distribution analysis method (BEDAM) and validated using the Grid Inhomogeneous Solvation Theory analysis. These new solvation parameters were used to study protein-ligand binding in two drug targets against the HIV-1 virus and improved the agreement between the calculated and the experimental binding affinities. This work illustrates how benchmark sets of high quality experimental binding affinity data and physics-based binding free energy models can be used to evaluate and optimize force fields for protein-ligand systems. Copyright © 2015 John Wiley & Sons, Ltd." @default.
- W1958906090 created "2016-06-24" @default.
- W1958906090 creator A5023494046 @default.
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- W1958906090 date "2015-08-10" @default.
- W1958906090 modified "2023-10-10" @default.
- W1958906090 title "Parameterization of an effective potential for protein-ligand binding from host-guest affinity data" @default.
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- W1958906090 doi "https://doi.org/10.1002/jmr.2489" @default.
- W1958906090 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4715590" @default.