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dc.contributor.authorYoo, Gu-
dc.contributor.authorBong, Ji-Hong-
dc.contributor.authorPark, Min-
dc.contributor.authorKang, Min-Jung-
dc.contributor.authorJose, Joachim-
dc.contributor.authorPyun, Jae-Chul-
dc.date.accessioned2024-01-20T12:02:02Z-
dc.date.available2024-01-20T12:02:02Z-
dc.date.created2021-09-04-
dc.date.issued2013-07-10-
dc.identifier.issn0141-0229-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/127874-
dc.description.abstractEscherichia coli cells with autodisplayed Z-domains could increase the sensitivity of immunoassays by immobilizing antibodies in a controlled orientation. In the work presented here, E. coli cells with autodisplayed Z-domains were immobilized to magnetic beads for subsequent immunoassay. In comparing conventional immunoassay using the E. coli cells with autodisplayed Z-domains, the magnetic-beadbased immunoassay improved immunoassay efficiency by minimizing the loss of E. coli cells during repeated centrifugation steps during washing. For the immobilization of E. coli cells to magnetic beads, the magnetic beads were modified with poly-L-lysine to bind to negatively charged E. coli cells. During the surface modification process, physical parameters such as the surface charge and size of the magnetic beads were analyzed to confirm the formation of E. coli-magnetic bead complexes. To test the feasibility of the magnetic-bead-based immunoassay, horseradish peroxidase (HRP) was used as a model analyte, and a biomarker for inflammatory diseases, C-reactive protein (CRP), was used for a demonstration of an application in medical diagnosis. (C) 2013 Elsevier Inc. All rights reserved.-
dc.languageEnglish-
dc.publisherELSEVIER SCIENCE INC-
dc.subjectC-REACTIVE PROTEIN-
dc.subjectESCHERICHIA-COLI-
dc.subjectANTIBODY IMMOBILIZATION-
dc.subjectSPR BIOSENSOR-
dc.subjectRECOMBINANT PROTEINS-
dc.subjectSURFACE DISPLAY-
dc.subjectOUTER-MEMBRANE-
dc.subjectLAYER-
dc.subjectIMMUNOSENSOR-
dc.subjectORIENTATION-
dc.titleMagnetic-bead-based immunoassay using E. coli cells with autodisplayed Z-domains-
dc.typeArticle-
dc.identifier.doi10.1016/j.enzmictec.2013.03.022-
dc.description.journalClass1-
dc.identifier.bibliographicCitationENZYME AND MICROBIAL TECHNOLOGY, v.53, no.2, pp.118 - 122-
dc.citation.titleENZYME AND MICROBIAL TECHNOLOGY-
dc.citation.volume53-
dc.citation.number2-
dc.citation.startPage118-
dc.citation.endPage122-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000321479700007-
dc.identifier.scopusid2-s2.0-84879017924-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.type.docTypeArticle-
dc.subject.keywordPlusC-REACTIVE PROTEIN-
dc.subject.keywordPlusESCHERICHIA-COLI-
dc.subject.keywordPlusANTIBODY IMMOBILIZATION-
dc.subject.keywordPlusSPR BIOSENSOR-
dc.subject.keywordPlusRECOMBINANT PROTEINS-
dc.subject.keywordPlusSURFACE DISPLAY-
dc.subject.keywordPlusOUTER-MEMBRANE-
dc.subject.keywordPlusLAYER-
dc.subject.keywordPlusIMMUNOSENSOR-
dc.subject.keywordPlusORIENTATION-
dc.subject.keywordAuthorAutodisplay-
dc.subject.keywordAuthorZ-domain-
dc.subject.keywordAuthorMagnetic bead-
dc.subject.keywordAuthorImmunoassay-
dc.subject.keywordAuthorSurface modification-
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