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In SilicoAnalysis of the Antigenic Properties of Iron-Regulated Proteins againstNeisseria meningitidis

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dc.contributor.authorRahman, Shahedur-
dc.contributor.authorBiswas, Chayon-
dc.contributor.authorBiswas, Polash Kumar-
dc.contributor.authorKader, Md Ashraful-
dc.contributor.authorAlam, S. M. Nur-
dc.contributor.authorSonne, Christian-
dc.contributor.authorKim, Ki-Hyun-
dc.date.accessioned2021-08-02T08:52:30Z-
dc.date.available2021-08-02T08:52:30Z-
dc.date.created2021-05-12-
dc.date.issued2020-09-
dc.identifier.issn2076-3417-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/8951-
dc.description.abstractNeisseria meningitidisis a commensal pathogen that causes infectious cerebrospinal disease in people of all ages. The multivariate role of six disease-causing polysaccharide serotypes is found to play a crucial role in developing vaccines (or general treatment strategies) to treat this emerging pathogen. Iron is a crucial transition metal forN. meningitidis. Proteomic analysis data could be valuable for vaccine design. Here, we conduct a comparative study using computational bioinformatic tools to identify the most effective iron-regulated outer membrane proteins (OMPs) as immunogenic targets for a potential vaccine againstN. meningitidis. The basic properties ofN. meningitidisOMPs are explored for flexibility, solubility, hydrophilicity, beta-turns, and overall antigenic probability. Results of our study suggest that iron-regulated OMPs are flexible and soluble in water with high densities of conformational B-cell epitopes. As such, they can be recommended as a novel candidate for a vaccine againstN. meningitidisbothin vitroandin vivo.-
dc.language영어-
dc.language.isoen-
dc.publisherMDPI-
dc.titleIn SilicoAnalysis of the Antigenic Properties of Iron-Regulated Proteins againstNeisseria meningitidis-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Ki-Hyun-
dc.identifier.doi10.3390/app10176113-
dc.identifier.scopusid2-s2.0-85090394794-
dc.identifier.wosid000571231000001-
dc.identifier.bibliographicCitationAPPLIED SCIENCES-BASEL, v.10, no.17, pp.1 - 12-
dc.relation.isPartOfAPPLIED SCIENCES-BASEL-
dc.citation.titleAPPLIED SCIENCES-BASEL-
dc.citation.volume10-
dc.citation.number17-
dc.citation.startPage1-
dc.citation.endPage12-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalResearchAreaPhysics-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryEngineering, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryPhysics, Applied-
dc.subject.keywordPlusANTIMICROBIAL PEPTIDE RESISTANCE-
dc.subject.keywordPlusOUTER-MEMBRANE PROTEIN-
dc.subject.keywordPlusHIGH EPITOPE DENSITY-
dc.subject.keywordPlusNEISSERIA-MENINGITIDIS-
dc.subject.keywordPlusDNA VACCINE-
dc.subject.keywordPlusFRPB-
dc.subject.keywordPlusIMMUNOGENICITY-
dc.subject.keywordPlusPREDICTION-
dc.subject.keywordPlusANTIBODIES-
dc.subject.keywordPlusMOLECULE-
dc.subject.keywordAuthorNeisseria meningitidis-
dc.subject.keywordAuthorvaccine development-
dc.subject.keywordAuthorepidemic disease-
dc.subject.keywordAuthorimmunogenicity-
dc.identifier.urlhttps://www.mdpi.com/2076-3417/10/17/6113-
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