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Accounting_for_the_Central_Role_of_Interfacial_Water_in_Protein-Ligand_Binding_Free_Energy_Calculations.pdf (889.18 kB)

Accounting for the Central Role of Interfacial Water in Protein-Ligand Binding Free Energy Calculations

preprint
submitted on 17.07.2020 and posted on 20.07.2020 by Ido Ben-Shalom, Zhixiong Lin, Brian Radak, Charles Lin, Woody Sherman, Michael K. Gilson
Rigorous binding free energy methods in drug discovery are growing in popularity due to a combination of methodological advances, improvements in computer hardware, and workflow automation. These calculations typically use molecular dynamics (MD) to sample from the Boltzmann distribution of conformational states. However, when part or all the binding site is inaccessible to bulk solvent, the time needed for water molecules to equilibrate between bulk solvent and the binding site can be well beyond what is practical with standard MD. This sampling limitation is problematic in relative binding free energy calculations, which compute the reversible work of converting Ligand 1 to Ligand 2 within the binding site. Thus, if Ligand 1 is smaller and/or more polar than Ligand 2, the perturbation may allow additional water molecules to occupy a region of the binding site. However, this change in hydration may not be captured by standard MD simulations and may therefore lead to errors in the computed free energy. We recently developed a hybrid Monte Carlo/MD (MC/MD) method, which speeds the equilibration of water between bulk solvent and buried cavities, while sampling from the intended distribution of states. Here, we report on the use of this approach in the context of alchemical binding free energy calculations. We find that using MC/MD markedly improves the accuracy of the calculations and also reduces hysteresis between the forward and reverse perturbations, relative to matched calculations using only MD with or without the crystallographic water molecules. The present method is available for use in the AMBER simulation software.

Funding

GM061300

GM100946

History

Email Address of Submitting Author

ibenshalom@health.ucsd.edu

Institution

University of California San Diego

Country

USA

ORCID For Submitting Author

0000-0002-7237-1690

Declaration of Conflict of Interest

MKG has an equity interest in and is a cofounder and scientific advisor of VeraChem LLC. ZL, BKR, CL and WS are employees of Silicon Therapeutics.

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