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dc.contributor.authorTung, Chun-Weien_US
dc.contributor.authorHo, Shinn-Yingen_US
dc.date.accessioned2014-12-08T15:14:15Z-
dc.date.available2014-12-08T15:14:15Z-
dc.date.issued2007-04-15en_US
dc.identifier.issn1367-4803en_US
dc.identifier.urihttp://dx.doi.org/10.1093/bioinformatics/btm061en_US
dc.identifier.urihttp://hdl.handle.net/11536/10903-
dc.description.abstractMotivation: Both modeling of antigen-processing pathway including major histocompatibility complex (MHC) binding and immunogenicity prediction of those MHC-binding peptides are essential to develop a computer-aided system of peptide-based vaccine design that is one goal of immunoinformatics. Numerous studies have dealt with modeling the immunogenic pathway but not the intractable problem of immunogenicity prediction due to complex effects of many intrinsic and extrinsic factors. Moderate affinity of the MHC-peptide complex is essential to induce immune responses, but the relationship between the affinity and peptide immunogenicity is too weak to use for predicting immunogenicity. This study focuses on mining informative physicochemical properties from known experimental immunogenicity data to understand immune responses and predict immunogenicity of MHC-binding peptides accurately. Results: This study proposes a computational method to mine a feature set of informative physicochemical properties from MHC class I binding peptides to design a support vector machine (SVM) based system (named POPI) for the prediction of peptide immunogenicity. High performance of POPI arises mainly from an inheritable bi-objective genetic algorithm, which aims to automatically determine the best number m out of 531 physicochemical properties, identify these m properties and tune SVM parameters simultaneously. The dataset consisting of 428 human MHC class I binding peptides belonging to four classes of immunogenicity was established from MHCPEP, a database of MHC-binding peptides (Brusic et al., 1998). POPI, utilizing the m = 23 selected properties, performs well with the accuracy of 64.72% using leave-one-out cross-validation, compared with two sequence alignment-based prediction methods ALIGN (54.91%) and PSI-BLAST (53.23%). POPI is the first computational system for prediction of peptide immunogenicity based on physicochemical properties.en_US
dc.language.isoen_USen_US
dc.titlePOPI: predicting immunogenicity of MHC class I binding peptides by mining informative physicochemical propertiesen_US
dc.typeArticleen_US
dc.identifier.doi10.1093/bioinformatics/btm061en_US
dc.identifier.journalBIOINFORMATICSen_US
dc.citation.volume23en_US
dc.citation.issue8en_US
dc.citation.spage942en_US
dc.citation.epage949en_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.department生物資訊及系統生物研究所zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.contributor.departmentInstitude of Bioinformatics and Systems Biologyen_US
dc.identifier.wosnumberWOS:000246293000004-
dc.citation.woscount39-
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