Sul-BertGRU: an ensemble deep learning method integrating information entropy-enhanced BERT and directional multi-GRU for S-sulfhydration sites prediction.

Xirun Wei, Qiao Ning, Kuiyang Che, Zhaowei Liu, Hui Li, Shikai Guo
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Abstract

Motivation: S-sulfhydration, a crucial post-translational protein modification, is pivotal in cellular recognition, signaling processes, and the development and progression of cardiovascular and neurological disorders, so identifying S-sulfhydration sites is crucial for studies in cell biology. Deep learning shows high efficiency and accuracy in identifying protein sites compared to traditional methods that often lack sensitivity and specificity in accurately locating nonsulfhydration sites. Therefore, we employ deep learning methods to tackle the challenge of pinpointing S-sulfhydration sites.

Results: In this work, we introduce a deep learning approach called Sul-BertGRU, designed specifically for predicting S-sulfhydration sites in proteins, which integrates multi-directional gated recurrent unit (GRU) and BERT. First, Sul-BertGRU proposes an information entropy-enhanced BERT (IE-BERT) to preprocess protein sequences and extract initial features. Subsequently, confidence learning is employed to eliminate potential S-sulfhydration samples from the nonsulfhydration samples and select reliable negative samples. Then, considering the directional nature of the modification process, protein sequences are categorized into left, right, and full sequences centered on cysteines. We build a multi-directional GRU to enhance the extraction of directional sequence features and model the details of the enzymatic reaction involved in S-sulfhydration. Ultimately, we apply a parallel multi-head self-attention mechanism alongside a convolutional neural network to deeply analyze sequence features that might be missed at a local level. Sul-BertGRU achieves sensitivity, specificity, precision, accuracy, Matthews correlation coefficient, and area under the curve scores of 85.82%, 68.24%, 74.80%, 77.44%, 55.13%, and 77.03%, respectively. Sul-BertGRU demonstrates exceptional performance and proves to be a reliable method for predicting protein S-sulfhydration sites.

Availability and implementation: The source code and data are available at https://github.com/Severus0902/Sul-BertGRU/.

动机S-硫酸化是蛋白质翻译后的一种重要修饰,在细胞识别、信号传导过程以及心血管和神经疾病的发生和发展中起着关键作用,因此识别S-硫酸化位点对细胞生物学研究至关重要。与传统方法相比,深度学习在识别蛋白质位点方面表现出高效率和高准确性,而传统方法在准确定位非硫酸化位点方面往往缺乏灵敏性和特异性。因此,我们采用深度学习方法来应对精确定位 S-硫酸化位点的挑战:在这项工作中,我们引入了一种名为 Sul-BertGRU 的深度学习方法,该方法是专为预测蛋白质中的 S-硫酸化位点而设计的,它整合了多向门控递归单元(GRU)和 BERT。首先,Sul-BertGRU 提出了一种信息熵增强 BERT(IE-BERT)来预处理蛋白质序列并提取初始特征。随后,利用置信度学习从非硫酸化样本中剔除潜在的硫酸化样本,并选择可靠的阴性样本。然后,考虑到修饰过程的方向性,以半胱氨酸为中心将蛋白质序列分为左序列、右序列和全序列。我们建立了一个多方向 GRU,以加强对方向性序列特征的提取,并对 S-硫酸化过程中涉及的酶反应细节进行建模。最后,我们将并行多头自注意机制与卷积神经网络(CNN)结合起来,深入分析可能在局部水平上遗漏的序列特征。Sul-BertGRU 的灵敏度、特异性、精确度、准确度、马太相关系数和曲线下面积分别达到了 85.82%、68.24%、74.80%、77.44%、55.13% 和 77.03%。Sul-BertGRU表现出卓越的性能,证明是预测蛋白质S-硫水合位点的可靠方法:源代码和数据见 https://github.com/Severus0902/Sul-BertGRU/.Supplementary 信息:补充数据可在 Bioinformatics online 上获取。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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