TY - JOUR
T1 - A Hyperbolic Discrete Diffusion 3D RNA Inverse Folding Model for Functional RNA Design
AU - Hou, Dongyue
AU - Zhang, Shuai
AU - Ma, Mengyao
AU - Lin, Hanbo
AU - Wan, Zheng
AU - Zhao, Hui
AU - Zhou, Ruian
AU - He, Xiao
AU - Wei, Xian
AU - Ju, Dianwen
AU - Zeng, Xian
N1 - Publisher Copyright:
© 2025 American Chemical Society.
PY - 2025/7/14
Y1 - 2025/7/14
N2 - Generative design of functional RNAs presents revolutionary opportunities for diverse RNA-based biotechnologies and biomedical applications. To this end, RNA inverse folding is a promising strategy for generatively designing new RNA sequences that can fold into desired topological structures. However, three-dimensional (3D) RNA inverse folding remains highly challenging due to limited availability of experimentally derived 3D structural data and unique characteristics of RNA 3D structures. In this study, we propose RIdiffusion, a hyperbolic denoising diffusion generative RNA inverse folding model, for 3D RNA design tasks. By embedding geometric features of RNA 3D structures and topological properties into hyperbolic space, RIdiffusion efficiently recovers the distribution of nucleotides for targeted RNA 3D structures based on limited training samples using a discrete diffusion model. We perform extensive evaluations on RIdiffusion using different data sets and strict data-splitting strategies and the results demonstrate that RIdiffusion consistently outperforms baseline generative models for RNA inverse folding. This study introduces RIdiffusion as a powerful tool for the generative design of functional RNAs, even in structure-data-scarce scenarios. By leveraging geometric deep learning, RIdiffusion enhances performance and holds promise for diverse downstream applications.
AB - Generative design of functional RNAs presents revolutionary opportunities for diverse RNA-based biotechnologies and biomedical applications. To this end, RNA inverse folding is a promising strategy for generatively designing new RNA sequences that can fold into desired topological structures. However, three-dimensional (3D) RNA inverse folding remains highly challenging due to limited availability of experimentally derived 3D structural data and unique characteristics of RNA 3D structures. In this study, we propose RIdiffusion, a hyperbolic denoising diffusion generative RNA inverse folding model, for 3D RNA design tasks. By embedding geometric features of RNA 3D structures and topological properties into hyperbolic space, RIdiffusion efficiently recovers the distribution of nucleotides for targeted RNA 3D structures based on limited training samples using a discrete diffusion model. We perform extensive evaluations on RIdiffusion using different data sets and strict data-splitting strategies and the results demonstrate that RIdiffusion consistently outperforms baseline generative models for RNA inverse folding. This study introduces RIdiffusion as a powerful tool for the generative design of functional RNAs, even in structure-data-scarce scenarios. By leveraging geometric deep learning, RIdiffusion enhances performance and holds promise for diverse downstream applications.
UR - https://www.scopus.com/pages/publications/105008272020
U2 - 10.1021/acs.jcim.5c00527
DO - 10.1021/acs.jcim.5c00527
M3 - 文章
AN - SCOPUS:105008272020
SN - 1549-9596
VL - 65
SP - 6568
EP - 6584
JO - Journal of Chemical Information and Modeling
JF - Journal of Chemical Information and Modeling
IS - 13
ER -