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Journal Article

Challenges encountered applying equilibrium and nonequilibrium binding free energy calculations

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Gapsys,  V.
Research Group of Computational Biomolecular Dynamics, MPI for biophysical chemistry, Max Planck Society;

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de Groot,  B. L.
Research Group of Computational Biomolecular Dynamics, MPI for biophysical chemistry, Max Planck Society;

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3332254.pdf
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Citation

Baumann, H. M., Gapsys, V., de Groot, B. L., & Mobley, D. L. (2021). Challenges encountered applying equilibrium and nonequilibrium binding free energy calculations. Journal of Physical Chemistry B, 125(17), 4241-4261. doi:10.1021/acs.jpcb.0c10263.


Cite as: http://hdl.handle.net/21.11116/0000-0008-E916-9
Abstract
Binding free energy calculations have become increasingly valuable to drive decision making in drug discovery projects. However, among other issues, inadequate sampling can reduce accuracy, limiting the value of the technique. In this paper, we apply absolute binding free energy calculations to ligands binding to T4 lysozyme L99A and HSP90 using equilibrium and nonequilibrium approaches. We highlight sampling problems encountered in these systems, such as slow side chain rearrangements and slow changes of water placement upon ligand binding. These same types of challenges are also likely to show up in other protein–ligand systems, and we propose some strategies to diagnose and test for such problems in alchemical free energy calculations. We also explore similarities and differences in how the equilibrium and the nonequilibrium approaches handle these problems. Our results show the large amount of work still to be done to make free energy calculations robust and reliable and provide insight for future research in this area.