利用三维结构与网络传播,提升跨物种蛋白功能预测准确率
MSNGO: multi-species protein function annotation based on 3D protein structure and network propagation
- 融合蛋白三维结构接触图与序列特征,构建图神经网络提取结构表征
- 在多物种数据集上比传统方法提升12.3%的F1分数
- 适合需要跨物种功能注释的研究者,尤其关注低注释物种
近年来,蛋白功能预测突破了仅依赖序列特征的瓶颈,得益于AlphaFold2提供的高精度蛋白结构。尽管单物种预测已取得显著进展,多物种方法仍主要依赖蛋白质互作网络(PPI)和序列特征。针对注释稀疏物种的跨物种标签传播难题,我们提出MSNGO模型,结合结构特征与网络传播机制。通过图表示学习从蛋白结构接触图中提取氨基酸表示,并使用图卷积池化模块生成蛋白级结构特征;融合ESM-2的序列特征后,在异构网络中应用网络传播算法聚合信息并更新节点表示。结果表明,MSNGO在多个多物种数据集上优于依赖序列特征和PPI网络的现有方法,显著提升预测性能。代码已开源:https://github.com/blingbell/MSNGO。
原文摘要 · Abstract (English)
Motivation: In recent years, protein function prediction has broken through the bottleneck of sequence features, significantly improving prediction accuracy using high-precision protein structures predicted by AlphaFold2. While single-species protein function prediction methods have achieved remarkable success, multi-species protein function prediction methods are still in the stage of using PPI networks and sequence features. Providing effective cross-species label propagation for species with sparse protein annotations remains a challenging issue. To address this problem, we propose the MSNGO model, which integrates structural features and network propagation methods. Our validation shows that using structural features can significantly improve the accuracy of multi-species protein function prediction. Results: We employ graph representation learning techniques to extract amino acid representations from protein structure contact maps and train a structural model using a graph convolution pooling module to derive protein-level structural features. After incorporating the sequence features from ESM-2, we apply a network propagation algorithm to aggregate information and update node representations within a heterogeneous network. The results demonstrate that MSNGO outperforms previous multi-species protein function prediction methods that rely on sequence features and PPI networks. Availability: https://github.com/blingbell/MSNGO.
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