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Mitochondria-Immobilized pH-Sensitive Off-On Fluorescent Probe

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dc.contributor.authorLee, Min Hee-
dc.contributor.authorPark, Nayoung-
dc.contributor.authorYi, Chunsik-
dc.contributor.authorHan, Ji Hye-
dc.contributor.authorHong, Ji Hye-
dc.contributor.authorKim, Kwang Pyo-
dc.contributor.authorKang, Dong Hoon-
dc.contributor.authorSessler, Jonathan L.-
dc.contributor.authorKang, Chulhun-
dc.contributor.authorKim, Jong Seung-
dc.date.accessioned2021-09-05T04:09:42Z-
dc.date.available2021-09-05T04:09:42Z-
dc.date.created2021-06-15-
dc.date.issued2014-10-08-
dc.identifier.issn0002-7863-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/97106-
dc.description.abstractWe report here a mitochondria-targetable pH-sensitive probe that allows for a quantitative measurement of mitochondrial pH changes, as well as the real-time monitoring of pH-related physiological effects in live cells. This system consists of a piperazine-linked naphthalimide as a fluorescence off-on signaling unit, a cationic triphenylphosphonium group for mitochondrial targeting, and a reactive benzyl chloride subunit for mitochondrial fixation. It operates well in a mitochondrial environment within whole cells and displays a desirable off-on fluorescence response to mitochondrial acidification. Moreover, this probe allows for the monitoring of impaired mitochondria undergoing mitophagic elimination as the result of nutrient starvation. It thus allows for the monitoring of the organelle-specific dynamics associated with the conversion between physiological and pathological states.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherAMER CHEMICAL SOC-
dc.subjectOXIDATIVE-PHOSPHORYLATION-
dc.subjectCARDIAC MITOCHONDRIA-
dc.subjectHEART-MITOCHONDRIA-
dc.subjectPROTEIN MUTANT-
dc.subjectLIVING CELLS-
dc.subjectIN-VIVO-
dc.subjectCALCIUM-
dc.subjectMITOPHAGY-
dc.subjectMEMBRANE-
dc.subjectTHIOREDOXIN-
dc.titleMitochondria-Immobilized pH-Sensitive Off-On Fluorescent Probe-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Jong Seung-
dc.identifier.doi10.1021/ja506301n-
dc.identifier.scopusid2-s2.0-84907942519-
dc.identifier.wosid000343026700032-
dc.identifier.bibliographicCitationJOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.136, no.40, pp.14136 - 14142-
dc.relation.isPartOfJOURNAL OF THE AMERICAN CHEMICAL SOCIETY-
dc.citation.titleJOURNAL OF THE AMERICAN CHEMICAL SOCIETY-
dc.citation.volume136-
dc.citation.number40-
dc.citation.startPage14136-
dc.citation.endPage14142-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusOXIDATIVE-PHOSPHORYLATION-
dc.subject.keywordPlusCARDIAC MITOCHONDRIA-
dc.subject.keywordPlusHEART-MITOCHONDRIA-
dc.subject.keywordPlusPROTEIN MUTANT-
dc.subject.keywordPlusLIVING CELLS-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlusCALCIUM-
dc.subject.keywordPlusMITOPHAGY-
dc.subject.keywordPlusMEMBRANE-
dc.subject.keywordPlusTHIOREDOXIN-
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