Abstract
Epitope prediction based on random peptide library screening has become a focus as a promising method in immunoinformatics research. Some novel software and web-based servers have been proposed in recent years and have succeeded in given test cases. However, since the number of available mimotopes with the relevant structure of template-target complex is limited, a systematic evaluation of these methods is still absent. In this study, a new benchmark dataset was defined. Using this benchmark dataset and a representative dataset, five examples of the most popular epitope prediction software products which are based on random peptide library screening have been evaluated. Using the benchmark dataset, in no method did performance exceed a 0.42 precision and 0.37 sensitivity, and the MCC scores suggest that the epitope prediction results of these software programs are greater than random prediction about 0.09–0.13; while using the representative dataset, most of the values of these performance measures are slightly improved, but the overall performance is still not satisfactory. Many test cases in the benchmark dataset cannot be applied to these pieces of software due to software limitations. Moreover chances are that these software products are overfitted to the small dataset and will fail in other cases. Therefore finding the correlation between mimotopes and genuine epitope residues is still far from resolved and much larger dataset for mimotope-based epitope prediction is desirable.
Highlights
A B-cell epitope is defined as a part of protein antigen recognized by either a particular B cell receptor (BCR) or a particular antibody molecule of the immune system [1]
B-cell epitope prediction is important for vaccine design, development of diagnostic reagents and for studies to elucidate the interactions between antigen and antibody on a molecular level
B-cell epitope prediction methods based on random peptide library screening has been constructed and was made available
Summary
A B-cell epitope is defined as a part of protein antigen recognized by either a particular B cell receptor (BCR) or a particular antibody molecule of the immune system [1]. It may be either a short contiguous stretch of amino acids, called a linear or continuous epitope, or consist of sequence segments that are brought together in spatial proximity when the protein is folded, called a conformational or discontinuous epitope [2]. The combination of experimental and computational approaches seems to be the best choice
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