用超图建模三维RNA设计,提升序列生成准确性
Harnessing Hypergraphs in Geometric Deep Learning for 3D RNA Inverse Folding
- 基于超图构建RNA骨架结构,捕捉高阶分子互作关系
- 在PDBBind和RNAsolo数据集上生成序列准确率超现有方法
- 适合生物设计、药物开发等领域的研究人员参考
RNA逆折叠问题是RNA设计中的关键挑战,旨在寻找能折叠成特定二级结构的核苷酸序列,这对分子稳定性和功能至关重要。该任务的复杂性源于序列与结构之间的复杂关系。本文提出名为HyperRNA的生成框架,采用编码-解码架构,利用超图进行RNA序列设计。具体包括三个部分:预处理阶段通过3珠粗粒化表示提取RNA骨架原子坐标构建图结构;编码阶段使用注意力嵌入模块和超图编码器捕捉高阶依赖关系与复杂生物分子互作;解码阶段以自回归方式生成RNA序列。在PDBBind和RNAsolo数据集上进行了定量与定性实验,评估RNA序列生成及RNA-蛋白复合物序列生成的逆折叠任务。结果表明,HyperRNA不仅优于现有RNA设计方法,还展示了超图在RNA工程中的潜力。
原文摘要 · Abstract (English)
The RNA inverse folding problem, a key challenge in RNA design, involves identifying nucleotide sequences that can fold into desired secondary structures, which are critical for ensuring molecular stability and function. The inherent complexity of this task stems from the intricate relationship between sequence and structure, making it particularly challenging. In this paper, we propose a framework, named HyperRNA, a generative model with an encoder-decoder architecture that leverages hypergraphs to design RNA sequences. Specifically, our HyperRNA model consists of three main components: preprocessing, encoding and decoding. In the preprocessing stage, graph structures are constructed by extracting the atom coordinates of RNA backbone based on 3-bead coarse-grained representation. The encoding stage processes these graphs, capturing higher order dependencies and complex biomolecular interactions using an attention embedding module and a hypergraph-based encoder. Finally, the decoding stage generates the RNA sequence in an autoregressive manner. We conducted quantitative and qualitative experiments on the PDBBind and RNAsolo datasets to evaluate the inverse folding task for RNA sequence generation and RNA-protein complex sequence generation. The experimental results demonstrate that HyperRNA not only outperforms existing RNA design methods but also highlights the potential of leveraging hypergraphs in RNA engineering.
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