利用机器学习对蛋白质-蛋白质相互作用进行分类时序列特征的重要性。

The protein journal Pub Date : 2024-02-01 Epub Date: 2023-12-19 DOI:10.1007/s10930-023-10168-8
Sini S Raj, S S Vinod Chandra
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引用次数: 0

摘要

蛋白质与蛋白质之间的相互作用对病毒进入细胞至关重要。了解相互作用的机制对于研究人类与病毒的关联、开发新的生物制剂和候选药物以及病毒感染和抗病毒反应至关重要。基于蛋白质序列数据分析人类-病毒蛋白质-蛋白质相互作用的实验方法耗时耗力,因此人们正在开发机器学习模型来预测相互作用并确定物种间的大规模相互作用组。本研究强调了序列特征在从蛋白质序列数据中对相互作用和非相互作用蛋白质进行分类方面的重要性。本研究提取了氨基酸组成(AAC)、二肽组成(DPC)、成组氨基酸组成(GAAC)、假氨基酸组成(PAAC)等高维氨基酸序列特征。特征提取后,创建了三个数据集:数据集 1 包含所有提取的特征。数据集 2 和 3 包含通过降维获得的最相关特征。为了分析高维特征的重要性及其在蛋白质-蛋白质相互作用中的参与情况,在三个数据集上训练了随机森林分类器。通过降维,模型表现出了极高的准确性,这表明降维无法捕捉到人类和病毒蛋白质之间相互作用的复杂性和潜在关系。由于保留了高维特征,因此有可能捕捉到与宿主-病原体关联类似的蛋白质-蛋白质相互作用的所有特征,从而开发出具有生物学意义的模型。我们提出的方法是一种更现实、更全面的分类模型,能为病毒学和药物开发带来更深刻的见解和更好的应用。
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Significance of Sequence Features in Classification of Protein-Protein Interactions Using Machine Learning.

Protein-protein interactions are crucial for the entry of viruses into the cell. Understanding the mechanism of interactions is essential in studying human-virus association, developing new biologics and drug candidates, as well as viral infections and antiviral responses. Experimental methods to analyze human-virus protein-protein interactions based on protein sequence data are time-consuming and labor-intensive, so machine learning models are being developed to predict interactions and determine large-scale interactomes between species. The present work highlights the importance of sequence features in classifying interacting and non-interacting proteins from the protein sequence data. Higher dimensional amino acid sequence features such as Amino Acid Composition (AAC), Dipeptide Composition (DPC), Grouped Amino Acid Composition (GAAC), Pseudo-Amino Acid Composition (PAAC) etc., are extracted. Following feature extraction, three datasets were created: Dataset 1 contains all of the extracted features. While Datasets 2 and 3 contain the most relevant features obtained through dimensionality reduction. To analyze the importance of high-dimensional features and their participation in protein-protein interactions, a random forest classifier is trained on three datasets. With dimensionality reduction, the model exhibited exceptional accuracy, indicating that dimensionality reduction fails to capture the complexity of interactions and the underlying relationships between human and viral proteins. As a result of retaining high-dimensional features, it is possible to capture all the characteristics of protein-protein interactions that resemble host-pathogen associations, leading to the development of biologically meaningful models. Our proposed approach is a more realistic and comprehensive classification model, leading to deeper insights and better applications in virology and drug development.

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