IApred: A versatile open-source tool for predicting protein antigenicity across diverse pathogens

Sebastian Miles, Gonzalo Menafra, Andrés Iriarte, Jose Alejandro Chabalgoity
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Abstract

Accurate prediction of protein antigenicity is crucial for vaccine development, diagnostic test design, and therapeutic protein engineering. However, existing tools face limitations in accessibility, computational efficiency, and pathogen diversity. Here, we present IApred, an open-source intrinsic antigenicity predictor that addresses these challenges. IApred employs a Support Vector Machine (SVM) model trained on a comprehensive dataset of 918 high-antigenicity proteins from diverse pathogens, including Gram-positive and Gram-negative bacteria, viruses, fungi, protozoa, and helminths. The model incorporates features derived from physicochemical properties, E-descriptors, amino acid dimers and small linear motifs (SLiMs) to predict the probability of a protein eliciting a humoral immune response. In external validation, IApred demonstrated superior balanced performance (ROC AUC = 0.761, sensitivity = 0.702, specificity = 0.706) compared to existing tools (VaxiJen 2.0, VaxiJen 3.0 and ANTIGENpro), while maintaining high computational efficiency (approximately 1000 sequences per minute). IApred's host-and-pathogen-agnostic nature and integration capability into bioinformatic pipelines makes it versatile for diverse applications. A web-based version of the software is available at https://smilesinformatics.com/iapred, while the software and training code are freely available on GitHub (https://github.com/sebamiles/IAPred) and Zenodo (https://doi.org/10.5281/zenodo.14578279)

Abstract Image

IApred:一个多功能的开源工具,用于预测不同病原体的蛋白质抗原性
准确预测蛋白质抗原性对疫苗开发、诊断试验设计和治疗性蛋白质工程至关重要。然而,现有的工具在可及性、计算效率和病原体多样性方面面临限制。在这里,我们提出了IApred,一个开源的内在抗原性预测器,解决了这些挑战。IApred采用了一个支持向量机(SVM)模型,该模型训练了918个高抗原性蛋白质的综合数据集,这些蛋白质来自不同的病原体,包括革兰氏阳性和革兰氏阴性细菌、病毒、真菌、原生动物和蠕虫。该模型结合了来自物理化学性质、e -描述符、氨基酸二聚体和小线性基序(SLiMs)的特征,以预测蛋白质引发体液免疫反应的概率。在外部验证中,与现有工具(VaxiJen 2.0、VaxiJen 3.0和ANTIGENpro)相比,IApred表现出更好的平衡性能(ROC AUC = 0.761,灵敏度= 0.702,特异性= 0.706),同时保持较高的计算效率(每分钟约1000个序列)。IApred的宿主和病原体不可知性以及与生物信息管道的集成能力使其适用于各种应用。该软件的网络版本可在https://smilesinformatics.com/iapred上获得,而软件和培训代码可在GitHub (https://github.com/sebamiles/IAPred)和Zenodo (https://doi.org/10.5281/zenodo.14578279)上免费获得。
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
Immunoinformatics (Amsterdam, Netherlands)
Immunoinformatics (Amsterdam, Netherlands) Immunology, Computer Science Applications
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