{"title":"Protein-Protein Interaction Prediction Model Based on ProtBert-BiGRU-Attention.","authors":"Qian Gao, Chi Zhang, Ming Li, Tianfei Yu","doi":"10.1089/cmb.2023.0297","DOIUrl":null,"url":null,"abstract":"<p><p>The physiological activities within cells are mainly regulated through protein-protein interactions (PPI). Therefore, studying protein interactions has become an essential part of researching protein function and mechanisms. Traditional biological experiments required for PPI prediction are expensive and time consuming. For this reason, many methods based on predicting PPI from protein sequences have been proposed in recent years. However, existing computational methods usually require the combination of evolutionary feature information of proteins to predict PPI docking situations. Because different relevant features of selected proteins are chosen, there may be differences in the predicted results for PPI. This article proposes a PPI prediction method based on the pretrained protein sequence model ProtBert, combined with the Bidirectional Gated Recurrent Unit (BiGRU) and attention mechanism. Only using protein sequence information and leveraging ProtBert's powerful ability to capture amino acid feature information, BiGRU is used for further feature extraction of the amino acid vectors output by ProtBert. The attention mechanism is then applied to enhance the focus on different amino acid features and improve the expression ability of protein sequence features, ultimately obtaining binary classification results for protein interactions. Experimental results show that our proposed ProtBert-BiGRU-Attention model has good predictive performance for PPI. Through relevant comparative experiments, it has been proven that our model performs well in protein binary prediction. Furthermore, through the ablation experiment of the model, different deep learning modules' contributions to the prediction have been demonstrated.</p>","PeriodicalId":15526,"journal":{"name":"Journal of Computational Biology","volume":" ","pages":"797-814"},"PeriodicalIF":1.4000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Computational Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1089/cmb.2023.0297","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/7/29 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0
Abstract
The physiological activities within cells are mainly regulated through protein-protein interactions (PPI). Therefore, studying protein interactions has become an essential part of researching protein function and mechanisms. Traditional biological experiments required for PPI prediction are expensive and time consuming. For this reason, many methods based on predicting PPI from protein sequences have been proposed in recent years. However, existing computational methods usually require the combination of evolutionary feature information of proteins to predict PPI docking situations. Because different relevant features of selected proteins are chosen, there may be differences in the predicted results for PPI. This article proposes a PPI prediction method based on the pretrained protein sequence model ProtBert, combined with the Bidirectional Gated Recurrent Unit (BiGRU) and attention mechanism. Only using protein sequence information and leveraging ProtBert's powerful ability to capture amino acid feature information, BiGRU is used for further feature extraction of the amino acid vectors output by ProtBert. The attention mechanism is then applied to enhance the focus on different amino acid features and improve the expression ability of protein sequence features, ultimately obtaining binary classification results for protein interactions. Experimental results show that our proposed ProtBert-BiGRU-Attention model has good predictive performance for PPI. Through relevant comparative experiments, it has been proven that our model performs well in protein binary prediction. Furthermore, through the ablation experiment of the model, different deep learning modules' contributions to the prediction have been demonstrated.
细胞内的生理活动主要通过蛋白质-蛋白质相互作用(PPI)来调节。因此,研究蛋白质相互作用已成为研究蛋白质功能和机制的重要组成部分。预测 PPI 所需的传统生物学实验既昂贵又耗时。因此,近年来提出了许多基于蛋白质序列预测 PPI 的方法。然而,现有的计算方法通常需要结合蛋白质的进化特征信息来预测 PPI 的对接情况。由于所选蛋白质的相关特征不同,PPI 的预测结果可能存在差异。本文提出了一种基于预训练蛋白质序列模型ProtBert,结合双向门控循环单元(BiGRU)和注意机制的PPI预测方法。BiGRU 仅使用蛋白质序列信息,并利用 ProtBert 捕获氨基酸特征信息的强大能力,对 ProtBert 输出的氨基酸向量进行进一步的特征提取。然后利用注意力机制加强对不同氨基酸特征的关注,提高蛋白质序列特征的表达能力,最终得到蛋白质相互作用的二元分类结果。实验结果表明,我们提出的 ProtBert-BiGRU-Attention 模型对 PPI 具有良好的预测性能。通过相关的对比实验证明,我们的模型在蛋白质二元预测方面表现良好。此外,通过模型的消融实验,不同深度学习模块对预测的贡献也得到了证明。
期刊介绍:
Journal of Computational Biology is the leading peer-reviewed journal in computational biology and bioinformatics, publishing in-depth statistical, mathematical, and computational analysis of methods, as well as their practical impact. Available only online, this is an essential journal for scientists and students who want to keep abreast of developments in bioinformatics.
Journal of Computational Biology coverage includes:
-Genomics
-Mathematical modeling and simulation
-Distributed and parallel biological computing
-Designing biological databases
-Pattern matching and pattern detection
-Linking disparate databases and data
-New tools for computational biology
-Relational and object-oriented database technology for bioinformatics
-Biological expert system design and use
-Reasoning by analogy, hypothesis formation, and testing by machine
-Management of biological databases