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One-Step Homogeneous Immunoassay for the Detection of Influenza Virus Using Switching Peptide and Graphene Quencher

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dc.contributor.authorKim, Hong-Rae-
dc.contributor.authorBong, Ji-Hong-
dc.contributor.authorKim, Tae-Hun-
dc.contributor.authorShin, Seung-Shick-
dc.contributor.authorKang, Min-Jung-
dc.contributor.authorShim, Won-Bo-
dc.contributor.authorLee, Do Young-
dc.contributor.authorSon, Dong Hee-
dc.contributor.authorPyun, Jae-Chul-
dc.date.accessioned2022-12-26T05:41:14Z-
dc.date.available2022-12-26T05:41:14Z-
dc.date.issued2022-09-
dc.identifier.issn1976-0280-
dc.identifier.issn2092-7843-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/909-
dc.description.abstractOne-step homogeneous immunoassay was developed for detecting influenza viruses A and B (Inf-A and Inf-B) using the switching peptide H2. As the fluorescence-labeled switching peptide dissociated from the binding pocket of detection antibodies, the fluorescence signal could be directly generated by the binding of Inf-A and Inf-B without washing (i.e., one-step immunoassay). For the one-step homogeneous immunoassay with detection antibodies in solution, graphene was labeled with the antibodies as a fluorescence quencher. To test the feasibility of the homogeneous one-step immunoassay, the stability of the antibody complex with the switching peptide was evaluated under different pH and salt conditions. The one-step homogeneous immunoassay with switching peptide was conducted using influenza virus antigens in phosphate-buffered saline and real samples with inactivated Inf-A and Inf-B spiked in serum. Finally, the one-step homogeneous immunoassay results were compared with those of commercially available lateral flow immunoassays.-
dc.format.extent8-
dc.language영어-
dc.language.isoENG-
dc.publisher한국바이오칩학회-
dc.titleOne-Step Homogeneous Immunoassay for the Detection of Influenza Virus Using Switching Peptide and Graphene Quencher-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.doi10.1007/s13206-022-00076-x-
dc.identifier.scopusid2-s2.0-85135269431-
dc.identifier.wosid000831026100002-
dc.identifier.bibliographicCitationBioChip Journal, v.16, no.3, pp 334 - 341-
dc.citation.titleBioChip Journal-
dc.citation.volume16-
dc.citation.number3-
dc.citation.startPage334-
dc.citation.endPage341-
dc.type.docTypeArticle-
dc.identifier.kciidART002877520-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalWebOfScienceCategoryBiochemical Research Methods-
dc.relation.journalWebOfScienceCategoryChemistry, Analytical-
dc.relation.journalWebOfScienceCategoryNanoscience & Nanotechnology-
dc.subject.keywordPlusFLUORESCENCE-
dc.subject.keywordPlusASSOCIATION-
dc.subject.keywordPlusPLATFORM-
dc.subject.keywordPlusMODEL-
dc.subject.keywordAuthorOne-step homogeneous immunoassay-
dc.subject.keywordAuthorSwitching peptide-
dc.subject.keywordAuthorInfluenza-A and influenza-B virus-
dc.subject.keywordAuthorLateral flow immunoassay-
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