Gao Qian, Zhang Chi, Li Ming, Yu Tianfei
College of Computer and Control Engineering, Qiqihar University, Qiqihar, China.
College of Life Science and Agriculture Forestry, Qiqihar University, Qiqihar, China.
J Comput Biol. 2024 Sep;31(9):797-814. doi: 10.1089/cmb.2023.0297. Epub 2024 Jul 29.
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。PPI预测所需的传统生物学实验成本高且耗时。因此,近年来提出了许多基于从蛋白质序列预测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对接情况。由于所选蛋白质的不同相关特征被选用,PPI的预测结果可能会有所不同。本文提出了一种基于预训练蛋白质序列模型ProtBert的PPI预测方法,结合双向门控循环单元(BiGRU)和注意力机制。仅使用蛋白质序列信息并利用ProtBert强大的捕捉氨基酸特征信息的能力,BiGRU用于对ProtBert输出的氨基酸向量进行进一步特征提取。然后应用注意力机制来增强对不同氨基酸特征的关注并提高蛋白质序列特征的表达能力,最终获得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-注意力模型对PPI具有良好的预测性能。通过相关对比实验,证明了我们的模型在蛋白质二元预测中表现良好。此外,通过模型的消融实验,展示了不同深度学习模块对预测的贡献。