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Generation and characterization of a monoclonal antibody against MERS-CoV targeting the spike protein using a synthetic peptide epitope-CpG-DNA-liposome complex

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dc.contributor.authorPark, Byoung Kwon-
dc.contributor.authorMaharjan, Sony-
dc.contributor.authorLee, Su In-
dc.contributor.authorKim, Jinsoo-
dc.contributor.authorBae, Joon-Yong-
dc.contributor.authorPark, Man-Seong-
dc.contributor.authorKwon, Hyung-Joo-
dc.date.accessioned2021-09-01T13:36:06Z-
dc.date.available2021-09-01T13:36:06Z-
dc.date.created2021-06-19-
dc.date.issued2019-06-30-
dc.identifier.issn1976-6696-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/64717-
dc.description.abstractMiddle East respiratory syndrome coronavirus (MERS-CoV) uses the spike (S) glycoprotein to recognize and enter target cells. In this study, we selected two epitope peptide sequences within the receptor binding domain (RBD) of the MERS-CoV S protein. We used a complex consisting of the epitope peptide of the MERS-CoV S protein and CpG-DNA encapsulated in liposome complex to immunize mice, and produced the monoclonal antibodies 506-2G10G5 and 492-1G10E4E2. The western blotting data showed that both monoclonal antibodies detected the S protein and immunoprecipitated the native form of the S protein. Indirect immunofluorescence and confocal analysis suggested strong reactivity of the antibodies towards the S protein of MERS-CoV virus infected Vero cells. Furthermore, the 506-2G10G5 monoclonal antibody significantly reduced plaque formation in MERS-CoV infected Vero cells compared to normal mouse IgG and 492-1G10E4E2. Thus, we successfully produced a monoclonal antibody directed against the RBD domain of the S protein which could be used in the development of diagnostics and therapeutic applications in the future.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherKOREAN SOCIETY BIOCHEMISTRY & MOLECULAR BIOLOGY-
dc.subjectCORONAVIRUS-
dc.subjectRECEPTOR-
dc.titleGeneration and characterization of a monoclonal antibody against MERS-CoV targeting the spike protein using a synthetic peptide epitope-CpG-DNA-liposome complex-
dc.typeArticle-
dc.contributor.affiliatedAuthorPark, Man-Seong-
dc.identifier.doi10.5483/BMBRep.2019.52.6.185-
dc.identifier.scopusid2-s2.0-85068991871-
dc.identifier.wosid000473211900007-
dc.identifier.bibliographicCitationBMB REPORTS, v.52, no.6, pp.397 - 402-
dc.relation.isPartOfBMB REPORTS-
dc.citation.titleBMB REPORTS-
dc.citation.volume52-
dc.citation.number6-
dc.citation.startPage397-
dc.citation.endPage402-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.identifier.kciidART002475755-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.subject.keywordPlusCORONAVIRUS-
dc.subject.keywordPlusRECEPTOR-
dc.subject.keywordAuthorB cell epitope-
dc.subject.keywordAuthorLipoplex (O)-
dc.subject.keywordAuthorMERS-CoV-
dc.subject.keywordAuthorMonoclonal antibody-
dc.subject.keywordAuthorSpike protein-
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