iLBE for Computational Identification of Linear B-cell Epitopes by Integrating Sequence and Evolutionary Features
- Author:
Hasan MD.MEHEDI
1
;
Khatun MST.SHAMIMA
;
Kurata HIROYUKI
Author Information
1. Department of Bioscience and Bioinformatics,Kyushu Institute of Technology,Iizuka,Fukuoka 820-8502,Japan
- Keywords:
Linear B-cell epitope;
BLAST;
Feature encoding;
Feature selection;
Random forest
- From:
Genomics, Proteomics & Bioinformatics
2020;18(5):593-600
- CountryChina
- Language:Chinese
-
Abstract:
Linear B-cell epitopes are critically important for immunological applications, such as vaccine design, immunodiagnostic test, and antibody production, as well as disease diagnosis and therapy. The accurate identification of linear B-cell epitopes remains challenging despite several dec-ades of research. In this work, we have developed a novel predictor, Identification of Linear B-cell Epitope (iLBE), by integrating evolutionary and sequence-based features. The successive feature vectors were optimized by a Wilcoxon-rank sum test. Then the random forest (RF) algorithm using the optimal consecutive feature vectors was applied to predict linear B-cell epitopes. We combined the RF scores by the logistic regression to enhance the prediction accuracy. iLBE yielded an area under curve score of 0.809 on the training dataset and outperformed other prediction models on a comprehensive independent dataset. iLBE is a powerful computational tool to identify the linear B-cell epitopes and would help to develop penetrating diagnostic tests. A web application with curated datasets for iLBE is freely accessible at http://kurata14.bio.kyutech.ac.jp/iLBE/.
