Toward Achieving Efficient and Accurate Ligand-Protein Unbinding with Deep Learning and Molecular Dynamics through RAVE

In this work, we demonstrate how to leverage our recent iterative deep learning all atom molecular dynamics (MD) technique Reweighted autoencoded variational Bayes for enhanced sampling (RAVE) (Ribeiro, Bravo, Wang, Tiwary, J. Chem. Phys. 2018, 149, 072301) for investigating ligand-protein unbinding mechanisms and calculating absolute binding free energies, OGb, when plagued with difficult to sample rare events. In order to do so, we introduce a simple but powerful extension to RAVE that allows learning a reaction coordinate expressed as a piecewise function that is linear over all intervals. Such an approach allows us to retain the physical interpretation of a RAVE-derived reaction coordinate while making the method more applicable to a wider range of complex biophysical problems. As we will demonstrate, using as our test-case the slow dissociation of benzene from the L99A variant of lysozyme, the RAVE extension led to observing an unbinding event in 100% of the independent all-atom MD simulations, all within 3-50 ns for a process that takes on an average close to few hundred milliseconds, which reflects a 7 orders of magnitude acceleration relative to straightforward MD. Furthermore, we will show that without the use of time-dependent biasing, clear back-and-forth movement between metastable intermediates was achieved during the various simulations, demonstrating the caliber of the RAVE-derived piecewise reaction coordinate and bias potential, which together drive efficient and accurate sampling of the ligand-protein dissociation event. Last, we report the results for Delta G(b), which via very short MD simulations, can form a strict lower-bound that is similar to 2-3 kcal/mol off from experiments. We believe that RAVE, together with its multidimensional extension that we introduce here, will be a useful tool for simulating the slow unbinding process of practical ligand protein complexes in an automated manner with minimal use of human intuition.