Machine-learning-based structural analysis of interactions between antibodies and antigens

IF 2 4区 生物学 Q2 BIOLOGY Biosystems Pub Date : 2024-07-02 DOI:10.1016/j.biosystems.2024.105264
Grace Zhang , Xiaohan Kuang , Yuhao Zhang , Yunchao Liu , Zhaoqian Su , Tom Zhang , Yinghao Wu
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Abstract

Computational analysis of paratope-epitope interactions between antibodies and their corresponding antigens can facilitate our understanding of the molecular mechanism underlying humoral immunity and boost the design of new therapeutics for many diseases. The recent breakthrough in artificial intelligence has made it possible to predict protein-protein interactions and model their structures. Unfortunately, detecting antigen-binding sites associated with a specific antibody is still a challenging problem. To tackle this challenge, we implemented a deep learning model to characterize interaction patterns between antibodies and their corresponding antigens. With high accuracy, our model can distinguish between antibody-antigen complexes and other types of protein-protein complexes. More intriguingly, we can identify antigens from other common protein binding regions with an accuracy of higher than 70% even if we only have the epitope information. This indicates that antigens have distinct features on their surface that antibodies can recognize. Additionally, our model was unable to predict the partnerships between antibodies and their particular antigens. This result suggests that one antigen may be targeted by more than one antibody and that antibodies may bind to previously unidentified proteins. Taken together, our results support the precision of antibody-antigen interactions while also suggesting positive future progress in the prediction of specific pairing.

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基于机器学习的抗体与抗原相互作用结构分析。
对抗体及其相应抗原之间的副位点-表位相互作用进行计算分析,有助于我们了解体液免疫的分子机制,并促进许多疾病的新疗法的设计。人工智能领域的最新突破使预测蛋白质-蛋白质相互作用并建立其结构模型成为可能。遗憾的是,检测与特定抗体相关的抗原结合位点仍然是一个具有挑战性的问题。为了应对这一挑战,我们采用了一种深度学习模型来描述抗体与其相应抗原之间的相互作用模式。我们的模型可以高精度地区分抗体-抗原复合物和其他类型的蛋白质-蛋白质复合物。更有趣的是,即使只有表位信息,我们也能从其他常见的蛋白质结合区域识别抗原,准确率超过 70%。这表明抗原表面有抗体可以识别的明显特征。此外,我们的模型无法预测抗体与其特定抗原之间的伙伴关系。这一结果表明,一种抗原可能被不止一种抗体靶向,而且抗体可能与之前未识别的蛋白质结合。综上所述,我们的研究结果支持了抗体与抗原相互作用的精确性,同时也预示着未来在预测特定配对方面将取得积极进展。
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来源期刊
Biosystems
Biosystems 生物-生物学
CiteScore
3.70
自引率
18.80%
发文量
129
审稿时长
34 days
期刊介绍: BioSystems encourages experimental, computational, and theoretical articles that link biology, evolutionary thinking, and the information processing sciences. The link areas form a circle that encompasses the fundamental nature of biological information processing, computational modeling of complex biological systems, evolutionary models of computation, the application of biological principles to the design of novel computing systems, and the use of biomolecular materials to synthesize artificial systems that capture essential principles of natural biological information processing.
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