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RiboSphere advances RNA structure modeling by integrating vector quantization with flow matching to capture modular structural motifs, addressing challenges posed by backbone flexibility and data scarcity. This approach enables high-fidelity reconstruction of 3D geometries while demonstrating effective transfer learning for inverse folding and ligand binding tasks in low-data regimes. The framework represents a significant methodological step forward using geometric transformers and discrete latent representations specific to biological macromolecules.
RiboSphere: Learning Unified and Efficient Representations of RNA Structures
arXiv:2603.19636v2 Announce Type: replace Abstract: Accurate RNA structure modeling remains difficult because RNA backbones are highly flexible, non-canonical interactions are prevalent, and experimentally determined 3D structures are comparatively scarce. We introduce RiboSphere, a framework that learns discrete geometric representations of RNA by combining vector quantization with flow matching. Our design is motivated by the modular organization of RNA architecture: complex folds are composed from recurring structural motifs. RiboSphere uses a geometric transformer encoder trained using mean-centered coordinates and random rotation augmentation to produce geometry-aware features, which are discretized with finite scalar quantization (FSQ) into a finite vocabulary of latent codes. Conditioned on these discrete codes, a flow-matching decoder reconstructs atomic coordinates, enabling high-fidelity structure generation. We find that the learned code indices are enriched for specific RNA motifs, suggesting that the model captures motif-level compositional structure rather than acting as a purely compressive bottleneck. Across benchmarks, RiboSphere achieves strong performance in structure reconstruction (RMSD 1.25,{\AA}, TM-score 0.84), and its pretrained discrete representations transfer effectively to inverse folding and RNA--ligand binding prediction, with robust generalization in data-scarce regimes. Code is available at https://github.com/Zhangz312/RiboSphere.
Abstract:Accurate RNA structure modeling remains difficult because RNA backbones are highly flexible, non-canonical interactions are prevalent, and experimentally determined 3D structures are comparatively scarce. We introduce RiboSphere, a framework that learns discrete geometric representations of RNA by combining vector quantization with flow matching. Our design is motivated by the modular organization of RNA architecture: complex folds are composed from recurring structural motifs. RiboSphere uses a geometric transformer encoder trained using mean-centered coordinates and random rotation augmentation to produce geometry-aware features, which are discretized with finite scalar quantization (FSQ) into a finite vocabulary of latent codes. Conditioned on these discrete codes, a flow-matching decoder reconstructs atomic coordinates, enabling high-fidelity structure generation. We find that the learned code indices are enriched for specific RNA motifs, suggesting that the model captures motif-level compositional structure rather than acting as a purely compressive bottleneck. Across benchmarks, RiboSphere achieves strong performance in structure reconstruction (RMSD 1.25,Å, TM-score 0.84), and its pretrained discrete representations transfer effectively to inverse folding and RNA--ligand binding prediction, with robust generalization in data-scarce regimes. Code is available at this https URL.
Machine Learning (cs.LG)
arXiv:2603.19636 [cs.LG]
(or arXiv:2603.19636v2 [cs.LG] for this version)
https://doi.org/10.48550/arXiv.2603.19636 Focus to learn more arXiv-issued DOI via DataCite
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