Label-free optical diagnosis of hepatitis B virus with genetically engineered fusion proteins

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dc.contributor.authorZheng, Shunko
dc.contributor.authorKim, Do-Kyunko
dc.contributor.authorPark, Tae Jungko
dc.contributor.authorLee, Seok Jaeko
dc.contributor.authorLee, SangYupko
dc.date.accessioned2010-11-12T07:38:44Z-
dc.date.available2010-11-12T07:38:44Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2010-07-
dc.identifier.citationTALANTA, v.82, no.2, pp.803 - 809-
dc.identifier.issn0039-9140-
dc.identifier.urihttp://hdl.handle.net/10203/19843-
dc.description.abstractA simple biosensing strategy for the diagnosis of patients with hepatitis B virus (HBV) was developed. This study can be divided into two themes, both of which utilized gold-binding polypeptide (GBP) fusion proteins: HBV surface antigen PreS2 (HBsAg) detection with GBP-fused single chain antibody (GBP-ScFv) and anti-HBsAg detection with GBP-HBsAg. These GBP-fusion proteins can directly bind onto the gold surface via the high binding affinity between the GBP and the gold surface, while at the same time, orient the recognition sites toward the sample for target binding. This one-step immobilization strategy, which greatly simplifies a fabrication process as well as maintaining biological activity of the recognition elements, can be applied to optical analytical methods, such as surface plasmon resonance (SPR) and localized surface plasmon resonance (LSPR). (C) 2010 Elsevier B.V. All rights reserved.-
dc.description.sponsorshipThis work was supported in part by the IT Leading R&D Support Project from the MKE through KEIT and by WCU (World Class University) program through the National Research Foundation of Korea funded by the Ministry of Education, Science and Technology (R32-2008-000-10142-0).en
dc.languageEnglish-
dc.language.isoen_USen
dc.publisherELSEVIER SCIENCE BV-
dc.titleLabel-free optical diagnosis of hepatitis B virus with genetically engineered fusion proteins-
dc.typeArticle-
dc.identifier.wosid000280375700057-
dc.identifier.scopusid2-s2.0-77955324690-
dc.type.rimsART-
dc.citation.volume82-
dc.citation.issue2-
dc.citation.beginningpage803-
dc.citation.endingpage809-
dc.citation.publicationnameTALANTA-
dc.identifier.doi10.1016/j.talanta.2010.05.059-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.contributor.localauthorLee, SangYup-
dc.contributor.nonIdAuthorKim, Do-Kyun-
dc.contributor.nonIdAuthorLee, Seok Jae-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorSurface plasmon resonance-
dc.subject.keywordAuthorLocalized surface plasmon resonance-
dc.subject.keywordAuthorBiosensor-
dc.subject.keywordAuthorHepatitis B virus-
dc.subject.keywordAuthorGold-binding polypeptide-
dc.subject.keywordAuthorFusion protein-
dc.subject.keywordPlusSURFACE-PLASMON RESONANCE-
dc.subject.keywordPlusGOLD-BINDING POLYPEPTIDE-
dc.subject.keywordPlusDIELECTRIC ENVIRONMENT-
dc.subject.keywordPlusDISPLAY-
dc.subject.keywordPlusIDENTIFICATION-
dc.subject.keywordPlusNANOPARTICLES-
dc.subject.keywordPlusBIOSENSORS-
dc.subject.keywordPlusPARTICLES-
dc.subject.keywordPlusINTERFACE-
dc.subject.keywordPlusDESIGN-
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