PreDBP-PLMs: Prediction of DNA-binding proteins based on pre-trained protein language models and convolutional neural networks

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-07-08 DOI:10.1016/j.ab.2024.115603
Dawei Qi, Chen Song, Taigang Liu
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Abstract

The recognition of DNA-binding proteins (DBPs) is the crucial step to understanding their roles in various biological processes such as genetic regulation, gene expression, cell cycle control, DNA repair, and replication within cells. However, conventional experimental methods for identifying DBPs are usually time-consuming and expensive. Therefore, there is an urgent need to develop rapid and efficient computational methods for the prediction of DBPs. In this study, we proposed a novel predictor named PreDBP-PLMs to further improve the identification accuracy of DBPs by fusing the pre-trained protein language model (PLM) ProtT5 embedding with evolutionary features as input to the classic convolutional neural network (CNN) model. Firstly, the ProtT5 embedding was combined with different evolutionary features derived from the position-specific scoring matrix (PSSM) to represent protein sequences. Then, the optimal feature combination was selected and input to the CNN classifier for the prediction of DBPs. Finally, the 5-fold cross-validation (CV), the leave-one-out CV (LOOCV), and the independent set test were adopted to examine the performance of PreDBP-PLMs on the benchmark datasets. Compared to the existing state-of-the-art predictors, PreDBP-PLMs exhibits an accuracy improvement of 0.5 % and 5.2 % on the PDB186 and PDB2272 datasets, respectively. It demonstrated that the proposed method could serve as a useful tool for the recognition of DBPs.

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PreDBP-PLMs:基于预训练蛋白质语言模型和卷积神经网络的 DNA 结合蛋白预测。
识别 DNA 结合蛋白(DBPs)是了解它们在遗传调控、基因表达、细胞周期控制、DNA 修复和细胞内复制等各种生物过程中作用的关键步骤。然而,鉴定 DBP 的传统实验方法通常耗时且昂贵。因此,迫切需要开发快速高效的计算方法来预测 DBPs。在这项研究中,我们提出了一种名为 "PreDBP-PLMs "的新型预测方法,通过将预先训练的蛋白质语言模型(PLM)ProtT5嵌入与进化特征融合,作为经典卷积神经网络(CNN)模型的输入,进一步提高了DBPs的鉴定准确率。首先,将 ProtT5 嵌入与从位置特异性评分矩阵(PSSM)中提取的不同进化特征相结合来表示蛋白质序列。然后,选出最佳特征组合并输入 CNN 分类器,用于预测 DBPs。最后,采用五倍交叉验证(CV)、留空CV(LOOCV)和独立集测试来检验PreDBP-PLMs在基准数据集上的性能。与现有的先进预测方法相比,PreDBP-PLMs 在 PDB186 和 PDB2272 数据集上的准确率分别提高了 0.5% 和 5.2%。这表明所提出的方法可以作为识别 DBPs 的有用工具。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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