Label-Free Electrochemical Diagnosis of Viral Antigens with Genetically Engineered Fusion Protein

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dc.contributor.authorHeo, Nam Suko
dc.contributor.authorZheng, Shunko
dc.contributor.authorYang, MinHoko
dc.contributor.authorLee, Seok Jaeko
dc.contributor.authorLee, Sang Yupko
dc.contributor.authorKim, Hwa-Jungko
dc.contributor.authorPark, Jung Younko
dc.contributor.authorLee, Chang-Sooko
dc.contributor.authorPark, Tae Jungko
dc.date.accessioned2013-03-12T18:12:14Z-
dc.date.available2013-03-12T18:12:14Z-
dc.date.created2012-10-16-
dc.date.created2012-10-16-
dc.date.created2012-10-16-
dc.date.created2012-10-16-
dc.date.issued2012-08-
dc.identifier.citationSENSORS, v.12, no.8, pp.10097 - 10108-
dc.identifier.issn1424-8220-
dc.identifier.urihttp://hdl.handle.net/10203/103106-
dc.description.abstractWe have developed a simple electrochemical biosensing strategy for the label-free diagnosis of hepatitis B virus (HBV) on a gold electrode surface. Gold-binding polypeptide (GBP) fused with single-chain antibody (ScFv) against HBV surface antigen (HBsAg), in forms of genetically engineered protein, was utilized. This GBP-ScFv fusion protein can directly bind onto the gold substrate with the strong binding affinity between the GBP and the gold surface, while the recognition site orients toward the sample for target binding at the same time. Furthermore, this one-step immobilization strategy greatly simplifies a fabrication process without any chemical modification as well as maintaining activity of biological recognition elements. This system allows specific immobilization of proteins and sensitive detection of targets, which were verified by surface plasmon resonance analysis and successfully applied to electrochemical cyclic voltammetry and impedance spectroscopy upto 0.14 ng/mL HBsAg.-
dc.languageEnglish-
dc.publisherMDPI AG-
dc.titleLabel-Free Electrochemical Diagnosis of Viral Antigens with Genetically Engineered Fusion Protein-
dc.typeArticle-
dc.identifier.wosid000308212100010-
dc.identifier.scopusid2-s2.0-84865352745-
dc.type.rimsART-
dc.citation.volume12-
dc.citation.issue8-
dc.citation.beginningpage10097-
dc.citation.endingpage10108-
dc.citation.publicationnameSENSORS-
dc.identifier.doi10.3390/s120810097-
dc.contributor.localauthorLee, Sang Yup-
dc.contributor.nonIdAuthorHeo, Nam Su-
dc.contributor.nonIdAuthorLee, Seok Jae-
dc.contributor.nonIdAuthorKim, Hwa-Jung-
dc.contributor.nonIdAuthorPark, Jung Youn-
dc.contributor.nonIdAuthorLee, Chang-Soo-
dc.contributor.nonIdAuthorPark, Tae Jung-
dc.description.isOpenAccessY-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorhepatitis B virus-
dc.subject.keywordAuthorGold-binding polypeptide-
dc.subject.keywordAuthorfusion protein-
dc.subject.keywordAuthorelectrochemical analysis-
dc.subject.keywordPlusPLASMON RESONANCE SPECTROSCOPY-
dc.subject.keywordPlusGOLD-BINDING POLYPEPTIDE-
dc.subject.keywordPlusCELL-SURFACE DISPLAY-
dc.subject.keywordPlusHEPATITIS-B-VIRUS-
dc.subject.keywordPlusBIOSENSOR-
dc.subject.keywordPlusIMMOBILIZATION-
dc.subject.keywordPlusIDENTIFICATION-
dc.subject.keywordPlusINFLUENZA-
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