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Cited 40 time in webofscience Cited 42 time in scopus
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dc.contributor.authorSeo, YJ-
dc.contributor.authorHwang, GT-
dc.contributor.authorKim, BH-
dc.date.accessioned2016-04-01T01:55:10Z-
dc.date.available2016-04-01T01:55:10Z-
dc.date.created2009-02-28-
dc.date.issued2006-06-06-
dc.identifier.issn0040-4039-
dc.identifier.other2006-OAK-0000005970-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/23999-
dc.description.abstractWe appended pyrene units covalently onto adenosine and uridine nucleosides (forming A(P) and U-P units, respectively) and then incorporated them into oligonucleotides such that they were positioned in complementary locations in opposite strands in the middle positions of hairpin stems. Systems 1 (A(P)U(P)) and 3 (A(P)A(P)) individually exhibit aromatic stacking between the opposing pyrene units in the stems of their hairpins and display in their spectra the photophysical properties of strongly red-shifted bands; in contrast, the (UUP)-U-P system 2 exhibits quenching spectra. Systems 1 (A(P)U(P)) and 3 (A(P)A(P)) behave as effective molecular beacons (MBs) that change color from green to blue upon duplex formation, whereas 2 ((UUP)-U-P) is an effective MB that changes the intensity of its fluorescence upon forming its perfectly matched duplex. (c) 2006 Elsevier Ltd. All rights reserved.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.relation.isPartOfTETRAHEDRON LETTERS-
dc.subjectfluorescence-
dc.subjectQuencher-free molecular beacon-
dc.subjectpi-pi stacking-
dc.subjectnucleotides-
dc.subjectDNA HYBRIDIZATION-
dc.subjectPROBING DNA-
dc.subjectOLIGONUCLEOTIDES-
dc.subjectFLUOROPHORES-
dc.subjectNUCLEOSIDE-
dc.subjectGUANINE-
dc.titleQuencher-free molecular beacon systems with two pyrene units in the stem region-
dc.typeArticle-
dc.contributor.college화학과-
dc.identifier.doi10.1016/j.tetlet.2006.04.002-
dc.author.googleSeo, YJ-
dc.author.googleHwang, GT-
dc.author.googleKim, BH-
dc.relation.volume47-
dc.relation.issue24-
dc.relation.startpage4037-
dc.relation.lastpage4039-
dc.contributor.id10142056-
dc.relation.journalTETRAHEDRON LETTERS-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationTETRAHEDRON LETTERS, v.47, no.24, pp.4037 - 4039-
dc.identifier.wosid000238012800015-
dc.date.tcdate2019-01-01-
dc.citation.endPage4039-
dc.citation.number24-
dc.citation.startPage4037-
dc.citation.titleTETRAHEDRON LETTERS-
dc.citation.volume47-
dc.contributor.affiliatedAuthorKim, BH-
dc.identifier.scopusid2-s2.0-33646368367-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc36-
dc.type.docTypeArticle-
dc.subject.keywordPlusDNA-
dc.subject.keywordPlusNUCLEOSIDE-
dc.subject.keywordPlusGUANINE-
dc.subject.keywordAuthorfluorescence-
dc.subject.keywordAuthorQuencher-free molecular beacon-
dc.subject.keywordAuthorpi-pi stacking-
dc.subject.keywordAuthornucleotides-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-

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김병현KIM, BYEANG HYEAN
Div of Advanced Materials Science
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