Abstract
Designing RNA sequences that fold into specific 3D structures is a fundamental challenge in therapeutics. Current RNA inverse folding methods typically condition on 3D backbone coordinates but the generation is limited to 1D discrete sequences. This ignores the continuous side-chain orientations, which are essential for overall structural stability. To address this issue, we explicitly introduce side-chain geometry into the RNA generative process. Unlike co-design frameworks that diffuse across separate raw spaces, we propose Geometric Optimized Latent Diffusion (\textbf{GOLD}), which project sequence and structure into a unified latent manifold. GOLD employs a novel GeoVAE to elegantly integrate discrete RNA sequences with continuous side-chain angles. By mapping these modalities into a single, smooth latent manifold, GOLD naturally facilitates a synergistic co-diffusion process. To enhance structural validity, we further introduce a training-free, gradient-guided sampling mechanism. By decoding the generated sequence probabilities and side-chain geometries into structures during the sampling process, we compute analytical gradients from physical constraints. This dynamic feedback actively guides the generated sequence to a physically stable state. Extensive experiments validate the superiority of GOLD, achieving state-of-the-art performance across sequence recovery, secondary structure validity, and 3D foldability metrics. Our code and data are publicly available at this https URL.
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URL
https://arxiv.org/abs/2610.22992
