Hamiltonian replica exchange augmented with diffusion-based generative models and importance sampling to assess biomolecular conformational basins and barriers

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Main Authors: Benayad, Zakarya, Stirnemann, Guillaume
Format: Preprint
Published: 2025
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author Benayad, Zakarya
Stirnemann, Guillaume
author_facet Benayad, Zakarya
Stirnemann, Guillaume
contents Enhanced sampling techniques are essential for exploring biomolecular conformational dynamics that occur on timescales inaccessible to conventional molecular dynamics (MD) simulations. This study introduces a framework that combines Hamiltonian replica exchange with solute tempering (REST2) with denoising diffusion probabilistic models (DDPMs) and importance sampling to enhance the mapping of conformational free-energy landscapes. Building on previous applications of DDPMs to temperature replica exchange (TREM), we propose two key improvements. First, we adapt the method to REST2 by treating potential energy as a fluctuating variable. This adaptation allows for more efficient sampling in large biomolecular systems. Second, to further improve resolution in high-barrier regions, we develop an iterative scheme combining replica exchange, DDPM, and importance sampling along known collective variables. Benchmarking on the mini-protein CLN025 demonstrates that DDPM-refined REST2 achieves comparable accuracy to TREM while requiring fewer replicas. Application to the enzyme PTP1B reveals a loop transition pathway consistent with prior complex biased simulations, showcasing the approach's ability to uncover high-barrier transitions with minimal computational overhead with respect to conventional replica exchange approaches. Overall, this hybrid strategy enables more efficient exploration of free-energy landscapes, expanding the utility of generative models in enhanced sampling simulations.
format Preprint
id arxiv_https___arxiv_org_abs_2505_08357
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Hamiltonian replica exchange augmented with diffusion-based generative models and importance sampling to assess biomolecular conformational basins and barriers
Benayad, Zakarya
Stirnemann, Guillaume
Statistical Mechanics
Biological Physics
Chemical Physics
Data Analysis, Statistics and Probability
Enhanced sampling techniques are essential for exploring biomolecular conformational dynamics that occur on timescales inaccessible to conventional molecular dynamics (MD) simulations. This study introduces a framework that combines Hamiltonian replica exchange with solute tempering (REST2) with denoising diffusion probabilistic models (DDPMs) and importance sampling to enhance the mapping of conformational free-energy landscapes. Building on previous applications of DDPMs to temperature replica exchange (TREM), we propose two key improvements. First, we adapt the method to REST2 by treating potential energy as a fluctuating variable. This adaptation allows for more efficient sampling in large biomolecular systems. Second, to further improve resolution in high-barrier regions, we develop an iterative scheme combining replica exchange, DDPM, and importance sampling along known collective variables. Benchmarking on the mini-protein CLN025 demonstrates that DDPM-refined REST2 achieves comparable accuracy to TREM while requiring fewer replicas. Application to the enzyme PTP1B reveals a loop transition pathway consistent with prior complex biased simulations, showcasing the approach's ability to uncover high-barrier transitions with minimal computational overhead with respect to conventional replica exchange approaches. Overall, this hybrid strategy enables more efficient exploration of free-energy landscapes, expanding the utility of generative models in enhanced sampling simulations.
title Hamiltonian replica exchange augmented with diffusion-based generative models and importance sampling to assess biomolecular conformational basins and barriers
topic Statistical Mechanics
Biological Physics
Chemical Physics
Data Analysis, Statistics and Probability
url https://arxiv.org/abs/2505.08357