Abstract

Upon invasion by foreign pathogens, specific antibodies can identify specific foreign antigens and disable them. As a result of this ability, antibodies can help with vaccine production and food allergen detection in patients. Many studies have focused on predicting linear B-cell epitopes, but only two prediction tools are currently available to predict the sub-type of an epitope. NIgPred was developed as a prediction tool for IgA, IgE, and IgG. NIgPred integrates various heterologous features with machine-learning approaches. Differently from previous studies, our study considered peptide-characteristic correlation and autocorrelation features. Sixty kinds of classifier were applied to construct the best prediction model. Furthermore, the genetic algorithm and hill-climbing algorithm were used to select the most suitable features for improving the accuracy and reducing the time complexity of the training model. NIgPred was found to be superior to the currently available tools for predicting IgE epitopes and IgG epitopes on independent test sets. Moreover, NIgPred achieved a prediction accuracy of 100% for the IgG epitopes of a coronavirus data set. NIgPred is publicly available at our website.

Highlights

  • IntroductionThere are many pathogens, such as bacteria, viruses, and allergens, which are present in daily life

  • For the problem of binary classification, the prediction results may be of four different types: True positives (TPs), false positives (FPs), false negatives (FNs), and true negatives (TNs)

  • We determined the differences in the average amino acid propensities of the IgA epitope data set, IgE epitope data set, IgG epitope data set, and non-BCE data sets

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Summary

Introduction

There are many pathogens, such as bacteria, viruses, and allergens, which are present in daily life. When foreign objects invade the human body, the immune system attacks them. The human immune system has natural immunity and acquired immunity against invading antigens. Innate immunity, supported by dendritic cells and macrophages, is the first line of defense and is not specific to the invading antigens. Compared with innate immunity, acquired immunity has specificity and diversity, and involves B-cells and T-cells

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