Accurate prediction of toxicity peptide and its function using multi-view tensor learning and latent semantic learning framework.

IF 5.4
Ke Yan, Shutao Chen, Bin Liu, Hao Wu
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Abstract

Motivation: Therapeutic peptide is an important ingredient in the treatment of various diseases and drug discovery. The toxicity of peptides is one of the major challenges in peptide drug therapy. With the abundance of therapeutic peptides generated in the post-genomics era, it is a challenge to promptly identify toxicity peptides using computational methods. Although several efforts have been made, few algorithms are designed to identify whether a query peptide exhibits toxicity. Considering the varied levels of biological activities, the toxicity peptides should be further classified into multi-functional peptides.

Results: This study introduces a two-level predictor, ToxPre-2L, developed using the multi-view tensor learning and latent semantic learning framework. The proposed method utilized multi-label learning with feature induced labels to avoid the redundancy of information from each view. Then the multi-view tensor learning was employed to establish the latent semantic information among different views, while low-rank constraint learning was leveraged to exploit the correlation information among multi-labels. Finally, we constructed an updated toxicity peptide benchmark dataset to assess the effectiveness of the proposed method. Experimental results demonstrated that ToxPre-2L achieves a better performance than alternative computational methods in the prediction of toxicity peptides and their multi-functional types.

Availability and implementation: The source code and data of ToxPre-2L can be accessed at http://bliulab.net/ToxPre-2L.

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基于多视图张量学习和潜在语义学习框架的毒性肽及其功能的准确预测。
动机:治疗肽是治疗各种疾病和发现药物的重要成分。多肽的毒性是多肽药物治疗的主要挑战之一。随着后基因组时代产生的治疗肽的丰富,使用计算方法迅速识别毒性肽是一个挑战。虽然已经做出了一些努力,但很少有算法被设计用于识别查询肽是否具有毒性。鉴于毒性肽具有不同程度的生物活性,应进一步将其分类为多功能肽。结果:本研究引入了一个使用多视图张量学习和潜在语义学习框架开发的两级预测器ToxPre-2L。该方法利用特征诱导标签的多标签学习来避免每个视图的信息冗余。然后利用多视图张量学习建立不同视图之间的潜在语义信息,利用低秩约束学习挖掘多标签之间的关联信息。最后,我们构建了一个更新的毒性肽基准数据集来评估所提出方法的有效性。实验结果表明,与其他计算方法相比,ToxPre-2L在预测毒性肽及其多功能类型方面具有更好的性能。可用性:ToxPre-2L的源代码和数据可在http://bliulab.net/ToxPre-2L.Supplementary上获取。信息:补充数据可在Bioinformatics在线获取。
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