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Cited 39 time in webofscience Cited 38 time in scopus
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dc.contributor.authorMa, DH-
dc.contributor.authorKim, D-
dc.contributor.authorAkisawa, T-
dc.contributor.authorLee, KH-
dc.contributor.authorKIM, KYONG TAI-
dc.contributor.authorAhn, KH-
dc.date.accessioned2016-04-01T07:57:45Z-
dc.date.available2016-04-01T07:57:45Z-
dc.date.created2015-06-18-
dc.date.issued2015-04-
dc.identifier.issn1861-4728-
dc.identifier.other2015-OAK-0000032728-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/27065-
dc.description.abstractA novel FRET couple of fluorescein is disclosed, and it was readily constructed by conjugating an amino-BODIPY dye, a new FRET donor, with fluorescein isocyanate. Its potential was demonstrated by a fluorescence sensing system for cysteine, which was prepared by introducing acryloyl groups to the fluorescein moiety. The FRET probe exhibited promising ratiometric response to cysteine with high selectivity and sensitivity in a buffer solution containing acetonitrile at a physiological pH of 7.4, but showed slow reactivity. This slow response was solved by addition of a surfactant, thus allowing ratiometric imaging and determination of the endogenous level of cysteine in cells in HEPES buffer, by confocal fluorescence microscopy. Imaging experiments toward various cells suggested that such aryl acrylate type probes are vulnerable to the ubiquitous esterase activity. For the selected C6 cell line, in which the esterase activity was minimal, the ratiometric quantification of cysteine level was demonstrated. The FRET probe was also applied to determine the level of cysteine in human blood plasma.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.relation.isPartOfCHEMISTRY-AN ASIAN JOURNAL-
dc.titleAn FITC-BODIPY FRET Couple: Application to Selective, Ratiometric Detection and Bioimaging of Cysteine-
dc.typeArticle-
dc.contributor.college화학과-
dc.identifier.doi10.1002/ASIA.201403073-
dc.author.googleMa, DH-
dc.author.googleKim, D-
dc.author.googleAkisawa, T-
dc.author.googleLee, KH-
dc.author.googleKim, KT-
dc.author.googleAhn, KH-
dc.relation.volume10-
dc.relation.issue4-
dc.relation.startpage894-
dc.relation.lastpage902-
dc.contributor.id10087916-
dc.relation.journalCHEMISTRY-AN ASIAN JOURNAL-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationCHEMISTRY-AN ASIAN JOURNAL, v.10, no.4, pp.894 - 902-
dc.identifier.wosid000351623600015-
dc.date.tcdate2019-02-01-
dc.citation.endPage902-
dc.citation.number4-
dc.citation.startPage894-
dc.citation.titleCHEMISTRY-AN ASIAN JOURNAL-
dc.citation.volume10-
dc.contributor.affiliatedAuthorKIM, KYONG TAI-
dc.contributor.affiliatedAuthorAhn, KH-
dc.identifier.scopusid2-s2.0-84925624790-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc17-
dc.description.scptc12*
dc.date.scptcdate2018-05-121*
dc.type.docTypeArticle-
dc.subject.keywordPlusRESONANCE ENERGY-TRANSFER-
dc.subject.keywordPlusLARGE EMISSION SHIFT-
dc.subject.keywordPlusFLUORESCENT-PROBE-
dc.subject.keywordPlusLIVING CELLS-
dc.subject.keywordPlusHOMOCYSTEINE-
dc.subject.keywordPlusGLUTATHIONE-
dc.subject.keywordPlusDESIGN-
dc.subject.keywordPlusTHIOLS-
dc.subject.keywordPlusDYES-
dc.subject.keywordPlusCHEMODOSIMETER-
dc.subject.keywordAuthoramino-bodipy-
dc.subject.keywordAuthorbioimaging-
dc.subject.keywordAuthorcysteine-
dc.subject.keywordAuthorfluorescence-
dc.subject.keywordAuthorFRET-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-

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김경태KIM, KYONG TAI
Dept of Life Sciences
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