Despite innovations in sampling techniques for molecular dynamics (MD), reliable prediction of protein-ligand binding free energies from MD remains a challenging problem, even in well studied model binding sites like the apolar cavity of T4 Lysozyme L99A.1 In this study, we model recent experimental results that show the progressive opening of the binding pocket in response to a series of homologous ligands.2 Even while using enhanced sampling techniques, we demonstrate that the predicted relative binding free energies (RBFE) are still highly sensitive to the initial protein conformational state. Particularly, we highlight the importance of sufficient sampling of protein conformational changes and possible techniques for addressing the issue. 1. Boyce, Sarah E., et al. "Predicting ligand binding affinity with alchemical free energy methods in a polar model binding site." Journal of molecular biology394.4 (2009): 747-763. 2. Merski, Matthew, et al. "Homologous ligands accommodated by discrete conformations of a buried cavity." Proceedings of the National Academy of Sciences 112.16 (2015): 5039-5044.

Sensitivity in predicted relative binding free energies from incremental ligand changes within a model binding site

251st National Meeting (2016)

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