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      SEPPA: a computational server for spatial epitope prediction of protein antigens

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          Abstract

          In recent years, a lot of efforts have been made in conformational epitope prediction as antigen proteins usually bind antibodies with an assembly of sequentially discontinuous and structurally compact surface residues. Currently, only a few methods for spatial epitope prediction are available with focus on single residue propensity scales or continual segments clustering. In the method of SEPPA, a concept of ‘unit patch of residue triangle’ was introduced to better describe the local spatial context in protein surface. Besides that, SEPPA incorporated clustering coefficient to describe the spatial compactness of surface residues. Validated by independent testing datasets, SEPPA gave an average AUC value over 0.742 and produced a successful pick-up rate of 96.64%. Comparing with peers, SEPPA shows significant improvement over other popular methods like CEP, DiscoTope and BEpro. In addition, the threshold scores for certain accuracy, sensitivity and specificity are provided online to give the confidence level of the spatial epitope identification. The web server can be accessed at http://lifecenter.sgst.cn/seppa/index.php. Batch query is supported.

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          Most cited references9

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          Prediction of residues in discontinuous B-cell epitopes using protein 3D structures.

          Discovery of discontinuous B-cell epitopes is a major challenge in vaccine design. Previous epitope prediction methods have mostly been based on protein sequences and are not very effective. Here, we present DiscoTope, a novel method for discontinuous epitope prediction that uses protein three-dimensional structural data. The method is based on amino acid statistics, spatial information, and surface accessibility in a compiled data set of discontinuous epitopes determined by X-ray crystallography of antibody/antigen protein complexes. DiscoTope is the first method to focus explicitly on discontinuous epitopes. We show that the new structure-based method has a better performance for predicting residues of discontinuous epitopes than methods based solely on sequence information, and that it can successfully predict epitope residues that have been identified by different techniques. DiscoTope detects 15.5% of residues located in discontinuous epitopes with a specificity of 95%. At this level of specificity, the conventional Parker hydrophilicity scale for predicting linear B-cell epitopes identifies only 11.0% of residues located in discontinuous epitopes. Predictions by the DiscoTope method can guide experimental epitope mapping in both rational vaccine design and development of diagnostic tools, and may lead to more efficient epitope identification.
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            The Immune Epitope Database and Analysis Resource: From Vision to Blueprint

            A planned repository of immune epitope data with associated analysis tools should be a boon to vaccine development
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              PEPITO: improved discontinuous B-cell epitope prediction using multiple distance thresholds and half sphere exposure.

              Accurate prediction of B-cell epitopes is an important goal of computational immunology. Up to 90% of B-cell epitopes are discontinuous in nature, yet most predictors focus on linear epitopes. Even when the tertiary structure of the antigen is available, the accurate prediction of B-cell epitopes remains challenging. Our predictor, PEPITO, uses a combination of amino-acid propensity scores and half sphere exposure values at multiple distances to achieve state-of-the-art performance. PEPITO achieves an area under the curve (AUC) of 75.4 on the Discotope dataset. Additionally, we benchmark PEPITO as well as the Discotope predictor on the more recent Epitome dataset, achieving AUCs of 68.3 and 66.0, respectively. PEPITO is available as part of the SCRATCH suite of protein structure predictors via www.igb.uci.edu. pfbaldi@ics.uci.edu Supplementary data are available at Bioinformatics online.
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                Author and article information

                Journal
                Nucleic Acids Res
                Nucleic Acids Res
                nar
                nar
                Nucleic Acids Research
                Oxford University Press
                0305-1048
                1362-4962
                1 July 2009
                1 July 2009
                22 May 2009
                22 May 2009
                : 37
                : Web Server issue
                : W612-W616
                Affiliations
                1Department of Biomedical Engineering, School of Life Sciences and Technology, Tongji University, Shanghai 200092, 2Shanghai Center for Bioinformation Technology, 100 Qinzhou Road, Shanghai 200235 and 3Bioinformatics Center, Key Lab of Systems Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China
                Author notes
                *To whom correspondence should be addressed. Tel: +86 21 5406 5003; Fax: +86 21 5406 5058; Email: zwcao@ 123456tongji.edu.cn
                Correspondence may also be addressed to Y.X. Li. Tel: +86 21 5406 5001; Fax: +86 21 5406 5058; Email: yxli@ 123456scbit.org
                Article
                gkp417
                10.1093/nar/gkp417
                2703964
                19465377
                f24a13f5-88ce-4151-b93f-265ed52de8ae
                © 2009 The Author(s)

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 4 February 2009
                : 24 April 2009
                : 6 May 2009
                Categories
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                Genetics
                Genetics

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