Enhanced Sampling for Conformational Changes and Molecular Mechanisms of Human NTHL1.

The functionalities of proteins rely on protein conformational changes during many processes. Identification of the protein conformations and capturing transitions among different conformations are important but extremely challenging in both experiments and simulations. In this work, we develop a machine learning based approach to identify a reaction coordinate that accelerates the exploration of protein conformational changes in molecular simulations. We implement our approach to study the conformational changes of human NTHL1 during DNA repair. Our results identified three distinct conformations: open (stable), closed (unstable), and bundle (stable). The existence of the bundle conformation can rationalize recent experimental observations. Comparison with an NTHL1 mutant demonstrates that a closely packed cluster of positively charged residues in the linker could be a factor to search when screening for genetic abnormalities. Results will lead to a better modulation of the DNA repair pathway to protect against carcinogenesis.

Prediction of the Peptide-TIM3 Binding Site in Inhibiting TIM3-Galectin 9 Binding Pathways.

T-cell immunoglobulin and mucin domain-containing protein-3 (TIM3) is an important receptor protein that modulates the immune system. The binding of TIM3 with Galectin 9 (GAL9) triggers immune system suppression, but the TIM3-GAL9 binding can be inhibited by binding of the peptide P26 to TIM3. A fast and accurate prediction of the P26-TIM3 binding site is crucial and a prerequisite for the investigation of P26-TIM3 interactions and TIM3-GAL9 binding pathways. Here, we present a machine learning approach, which considers protein conformational changes, to quickly identify the ligand-binding site on TIM3. Our results show that the P26 binding site is located near the C″-D loop of TIM3. Further simulations show that the binding pose is stabilized by a variety of electrostatic and hydrophobic interactions. Binding of P26 can alter the conformations of nearby glycan side chains on TIM3, providing possible mechanisms of how P26 inhibits TIM3-GAL9 binding pathways. The insights from this work will facilitate the identification of other peptides or antibodies that may also inhibit the TIM3-GAL9 pathways and eventually lead to improved attempts in the modulation of the TIM3-GAL9 immunosuppression pathways. The strategies and machine learning method can be generalized to study ligand-receptor binding when the conformational changes during the binding are important.

LINES: Log-Probability Estimation via Invertible Neural Networks for Enhanced Sampling.

It is very challenging to sample a molecular process with large activation energies using molecular dynamics simulations. Current enhanced sampling methodologies, such as umbrella sampling and metadynamics, rely on the identification of appropriate reaction coordinates for a system. In this paper, we developed a method for log-probability estimation via invertible neural networks for enhanced sampling (LINES). This iterative scheme utilizes a normalizing flow machine learning model to learn the underlying free energy surface (FES) of a system as a function of molecular coordinates and then applies a gradient-based optimization method to the learned normalizing flow to identify reaction coordinates. A biasing potential is then evaluated over a tabulated grid of the reaction coordinate values, which can be applied to the next round of simulations for enhanced sampling, resulting in more efficient sampling. We tested the accuracy and efficiency of the LINES method in sampling the FES using the alanine dipeptide system. We also demonstrated the effectiveness of identification of reaction coordinates through simulation of cyclobutanol unbinding from ß-cyclodextrin and the folding/unfolding of CLN025─a variant of the peptide Chignolin. The LINES method can be extended to the study of large-scale protein systems with complex nonlinear reaction pathways.