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dc.contributor.authorCho, M-
dc.contributor.authorKim, Y-
dc.contributor.authorHan, SY-
dc.contributor.authorMin, K-
dc.contributor.authorRahman, A-
dc.contributor.authorShim, YB-
dc.contributor.authorBan, C-
dc.date.accessioned2016-04-01T01:22:36Z-
dc.date.available2016-04-01T01:22:36Z-
dc.date.created2009-02-28-
dc.date.issued2008-02-29-
dc.identifier.issn1976-6696-
dc.identifier.other2008-OAK-0000007716-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/22791-
dc.description.abstractThe folding of aptamer immobilized on an Au electrode was successfully detected using label-free electrochemical methods. A thrombin binding DNA aptamer was used as a model system in the presence of various monovalent cations. Impedance spectra showed that the extent to which monovalent cations assist in folding of aptamer is ordered as K+ > NH4+ > Na+ > Cs+. Our XPS analysis also showed that K+ and NH4+ caused a conformational change of the aptamer in which it forms a stable complex with these monovalent ions. Impedance results for the interaction between aptamer and thrombin indicated that thrombin interacts more with folded aptamer than with unfolded aptamer. The EQCM technique provided a quantitative analysis of these results. In particular, the present impedance results showed that thrombin participates a folding of aptamer to some extent and XPS analysis confirmed that thrombin stabilizes and induces the folding of aptamer.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherKOREAN SOCIETY BIOCHEMISTRY & MOLECULAR BIOLOGY-
dc.relation.isPartOfBMB REPORTS-
dc.subjectaptamer folding-
dc.subjectimpedance-
dc.subjectthrombin-
dc.subjectthrombin aptamer-
dc.subjectXPS-
dc.subjectFLUORESCENCE ANISOTROPY-
dc.subjectIMPEDANCE SPECTROSCOPY-
dc.subjectPROTEIN BIOSENSOR-
dc.subjectRECOGNITION-
dc.subjectAPTASENSOR-
dc.subjectCOMPLEX-
dc.subjectSWITCH-
dc.subjectDNA-
dc.titleDetection for folding of the thrombin binding aptamer using label-free electrochemical methods-
dc.typeArticle-
dc.contributor.college화학과-
dc.identifier.doi10.5483/BMBRep.2008.41.2.126-
dc.author.googleCho, M-
dc.author.googleKim, Y-
dc.author.googleHan, SY-
dc.author.googleMin, K-
dc.author.googleRahman, A-
dc.author.googleShim, YB-
dc.author.googleBan, C-
dc.relation.volume41-
dc.relation.issue2-
dc.relation.startpage126-
dc.relation.lastpage131-
dc.contributor.id10085220-
dc.relation.journalBMB REPORTS-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCIE-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationBMB REPORTS, v.41, no.2, pp.126 - 131-
dc.identifier.wosid000255359500006-
dc.date.tcdate2019-01-01-
dc.citation.endPage131-
dc.citation.number2-
dc.citation.startPage126-
dc.citation.titleBMB REPORTS-
dc.citation.volume41-
dc.contributor.affiliatedAuthorBan, C-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc8-
dc.type.docTypeArticle-
dc.subject.keywordPlusFLUORESCENCE ANISOTROPY-
dc.subject.keywordPlusIMPEDANCE SPECTROSCOPY-
dc.subject.keywordPlusPROTEIN BIOSENSOR-
dc.subject.keywordPlusRECOGNITION-
dc.subject.keywordPlusAPTASENSOR-
dc.subject.keywordPlusCOMPLEX-
dc.subject.keywordPlusSWITCH-
dc.subject.keywordPlusDNA-
dc.subject.keywordAuthoraptamer folding-
dc.subject.keywordAuthorimpedance-
dc.subject.keywordAuthorthrombin-
dc.subject.keywordAuthorthrombin aptamer-
dc.subject.keywordAuthorXPS-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-

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Dept of Chemistry
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