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BioMD: All-atom Generative Model for Biomolecular Dynamics Simulation

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arxiv 2509.02642 v1 pith:EUSOEM5I submitted 2025-09-02 physics.chem-ph cs.AI

BioMD: All-atom Generative Model for Biomolecular Dynamics Simulation

classification physics.chem-ph cs.AI
keywords biomdcomputationalbiomoleculardatasetsdynamicsunbindingall-atomchemistry
verification ladder T0 review T1 audit T2 compute T3 formal T4 reserved
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Molecular dynamics (MD) simulations are essential tools in computational chemistry and drug discovery, offering crucial insights into dynamic molecular behavior. However, their utility is significantly limited by substantial computational costs, which severely restrict accessible timescales for many biologically relevant processes. Despite the encouraging performance of existing machine learning (ML) methods, they struggle to generate extended biomolecular system trajectories, primarily due to the lack of MD datasets and the large computational demands of modeling long historical trajectories. Here, we introduce BioMD, the first all-atom generative model to simulate long-timescale protein-ligand dynamics using a hierarchical framework of forecasting and interpolation. We demonstrate the effectiveness and versatility of BioMD on the DD-13M (ligand unbinding) and MISATO datasets. For both datasets, BioMD generates highly realistic conformations, showing high physical plausibility and low reconstruction errors. Besides, BioMD successfully generates ligand unbinding paths for 97.1% of the protein-ligand systems within ten attempts, demonstrating its ability to explore critical unbinding pathways. Collectively, these results establish BioMD as a tool for simulating complex biomolecular processes, offering broad applicability for computational chemistry and drug discovery.

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  1. Spectral Diffusion for Protein Dynamics

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    Diffusion over DCT spectral volumes of Cα displacements yields fast, temperature-conditioned protein trajectories with RMSF Pearson r of 0.844 on held-out mdCATH.