InteracTor: Feature engineering and explainable AI for profiling protein structure-interaction-function relationships.

IF 3.6 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Jose Cleydson F Silva, Layla Schuster, Nick Sexson, Melissa Erdem, Ryan Hulke, Matias Kirst, Marcio F R Resende, Raquel Dias
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引用次数: 0

Abstract

Characterizing protein families' structural and functional diversity is essential for understanding their biological roles. Traditional analyses often focus on primary and secondary structures, which may not fully capture complex protein interactions. Here we introduce InteracTor, a novel toolkit that extracts multimodal features from protein three-dimensional (3D) structures, including interatomic interactions like hydrogen bonds, van der Waals forces, and hydrophobic contacts. By integrating eXplainable Artificial Intelligence (XAI) techniques, we quantified the importance of the extracted features in the classification of protein structural and functional families. InteracTor's interpref features enable mechanistic insights into the determinants of protein structure, function, and dynamics, offering a transparent means to assess their predictive power within machine learning models. Interatomic interaction features extracted by InteracTor demonstrated superior predictive power for protein family classification compared to features based solely on primary or secondary structure, revealing the importance of considering specific tertiary contacts in computational protein analysis. This work provides a robust framework for future studies aiming to enhance the capabilities of models for protein function prediction and drug discovery.

InteracTor:用于分析蛋白质结构-相互作用-功能关系的特征工程和可解释的AI。
表征蛋白质家族的结构和功能多样性对于理解它们的生物学作用至关重要。传统的分析通常侧重于一级和二级结构,这可能无法完全捕获复杂的蛋白质相互作用。在这里,我们介绍InteracTor,一个新的工具箱,从蛋白质三维(3D)结构中提取多模态特征,包括原子间相互作用,如氢键、范德华力和疏水接触。通过整合可解释人工智能(eXplainable Artificial Intelligence, XAI)技术,我们量化了提取的特征在蛋白质结构和功能家族分类中的重要性。InteracTor的解释功能使我们能够对蛋白质结构、功能和动态的决定因素进行机械洞察,提供了一种透明的方法来评估机器学习模型中的预测能力。与仅基于一级或二级结构的特征相比,InteracTor提取的原子间相互作用特征对蛋白质家族分类的预测能力更强,这揭示了在计算蛋白质分析中考虑特定三级接触的重要性。这项工作为未来的研究提供了一个强大的框架,旨在提高模型在蛋白质功能预测和药物发现方面的能力。
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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来源期刊
PLoS Computational Biology
PLoS Computational Biology BIOCHEMICAL RESEARCH METHODS-MATHEMATICAL & COMPUTATIONAL BIOLOGY
CiteScore
7.10
自引率
4.70%
发文量
820
审稿时长
2.5 months
期刊介绍: PLOS Computational Biology features works of exceptional significance that further our understanding of living systems at all scales—from molecules and cells, to patient populations and ecosystems—through the application of computational methods. Readers include life and computational scientists, who can take the important findings presented here to the next level of discovery. Research articles must be declared as belonging to a relevant section. More information about the sections can be found in the submission guidelines. Research articles should model aspects of biological systems, demonstrate both methodological and scientific novelty, and provide profound new biological insights. Generally, reliability and significance of biological discovery through computation should be validated and enriched by experimental studies. Inclusion of experimental validation is not required for publication, but should be referenced where possible. Inclusion of experimental validation of a modest biological discovery through computation does not render a manuscript suitable for PLOS Computational Biology. Research articles specifically designated as Methods papers should describe outstanding methods of exceptional importance that have been shown, or have the promise to provide new biological insights. The method must already be widely adopted, or have the promise of wide adoption by a broad community of users. Enhancements to existing published methods will only be considered if those enhancements bring exceptional new capabilities.
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