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A Hyperbolic Discrete Diffusion 3D RNA Inverse Folding Model for Functional RNA Design

  • Dongyue Hou
  • , Shuai Zhang
  • , Mengyao Ma
  • , Hanbo Lin
  • , Zheng Wan
  • , Hui Zhao
  • , Ruian Zhou
  • , Xiao He*
  • , Xian Wei*
  • , Dianwen Ju*
  • , Xian Zeng*
  • *此作品的通讯作者
  • Fudan University
  • Byterna Therapeutics
  • East China Normal University
  • Adelaide University

科研成果: 期刊稿件文章同行评审

摘要

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.

源语言英语
页(从-至)6568-6584
页数17
期刊Journal of Chemical Information and Modeling
65
13
DOI
出版状态已出版 - 14 7月 2025

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