Ab initio side-chain sampling with PUD+ enables high-fidelity protein dynamics across AI-driven and classical simulations

The fidelity of molecular dynamics (MD) simulations fundamentally depends on the quality and coverage of the ab initio data used to parameterize the underlying force field, yet the role of side-chain conformational space remains insufficiently explored. In this study, we systematically investigate how comprehensive ab initio sampling of dipeptide conformations - specifically targeting side-chain degrees of freedom - impacts force field accuracy and MD simulation predictive power. We present the Protein Unit Dataset Plus (PUD+), a 40-million-conformation quantum mechanical dataset featuring unprecedented coverage of both backbone and side-chain conformational space. Machine learning force fields trained on PUD+ and integrated into AI2BMD simulations demonstrate superior energy and force prediction accuracy, capturing high-fidelity protein folding dynamics and the conformational flexibility of long-side-chain systems. Furthermore, leveraging PUD+ to reparameterize the CMAP term of the classical ff19SB force field markedly improves the description of intrinsically disordered protein (IDP) dynamics and IDP-ligand binding. Collectively, these results demonstrate that ab initio sampling of dipeptide side-chain conformations enables high-fidelity modeling of protein dynamics across both AI-driven and classical simulation paradigms.