Accurate prediction of RNA tertiary structure remains a central challenge in structural biology, yet existing computational approaches face fundamental limitations arising from the ruggedness of the RNA free-energy landscape and the scarcity of experimentally resolved structures. Here we present RNADaemon, a framework that formulates RNA tertiary structure prediction as a Markov Decision Process and trains a Soft Actor-Critic agent to apply adaptive external force-field biases that steer all-atom molecular dynamics toward native-like conformations to minimize the eRMSD metric. Trained on 479 monomeric RNA structures and evaluated on 14 test cases from CASP16, RNA-Puzzles, and the PDB, the agent trains stably, approaches SimRNA and FARFAR2 in median RMSD, and recovers the global fold of most reference structures. However, performance remains markedly inferior to that of AlphaFold 3 and trRosettaRNA. We identify the scalar Bellman error as a fundamental information bottleneck that currently limits the performance of the agent. To our knowledge, this is the first application of continuous-action deep reinforcement learning (RL) with all-atom force fields to RNA tertiary structure prediction. This study establishes a benchmark for future comparisons and provides diagnostic insights for RL-guided RNA structure modeling.
No takes yet. Share an insight, caveat, or question.
Xu et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: