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Discovery of an Ultra-rapid and Sensitive Lysosomal Fluorescence Lipophagy Process

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dc.contributor.authorKim, Jong Seung-
dc.contributor.authorZhang, Hong-
dc.contributor.authorShi, Lei-
dc.contributor.authorLi, Kun-
dc.contributor.authorLiu, Xin-
dc.contributor.authorWon, Miae-
dc.contributor.authorLiu, Yan-Zhao-
dc.contributor.authorChoe, Youmi-
dc.contributor.authorLiu, Xin-Yao-
dc.contributor.authorLiu, Yan-Hong-
dc.contributor.authorChen, Shan-Yong-
dc.contributor.authorYu, Kang-Kang-
dc.contributor.authorYu, Xiao-Qi-
dc.date.accessioned2022-04-18T06:41:43Z-
dc.date.available2022-04-18T06:41:43Z-
dc.date.created2022-04-18-
dc.date.issued2022-03-07-
dc.identifier.issn1433-7851-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/140265-
dc.description.abstractNon-invasive dynamic tracking of lysosomes and their interactions with other organelles is important for the study of lysosomal function and related diseases. However, many fluorescent dyes developed so far to target lysosomes cannot be used to monitor these processes due to the high concentrations required for imaging, long cell penetration times, and non-ideal photostability. In this regard, we synthesized three lysosomal targeting probes with large Stokes shifts, good stability, and high brightness. The Q-P-ARh dye, developed by us for the first time, can stain lysosomes at ultra-low concentrations (1.0 nM) without affecting the physiological functions of the lysosomes. More importantly, its excellent anti-interference ability and ultrafast lysosomal staining ability (within 1.0 min) clearly monitored the entire dynamic process of lipophagy. Ultimately, this method can greatly contribute to the study of autophagy pathways. This novel fluorescence platform shows great promise for the development of biological probes for application in pathological environments.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.subjectAUTOPHAGY-
dc.subjectPROBES-
dc.subjectCELLS-
dc.subjectDIFFERENTIATION-
dc.subjectADIPOCYTES-
dc.subjectMODEL-
dc.subjectDYES-
dc.titleDiscovery of an Ultra-rapid and Sensitive Lysosomal Fluorescence Lipophagy Process-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Jong Seung-
dc.identifier.doi10.1002/anie.202116439-
dc.identifier.scopusid2-s2.0-85122728033-
dc.identifier.wosid000742625100001-
dc.identifier.bibliographicCitationANGEWANDTE CHEMIE-INTERNATIONAL EDITION, v.61, no.11-
dc.relation.isPartOfANGEWANDTE CHEMIE-INTERNATIONAL EDITION-
dc.citation.titleANGEWANDTE CHEMIE-INTERNATIONAL EDITION-
dc.citation.volume61-
dc.citation.number11-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusAUTOPHAGY-
dc.subject.keywordPlusPROBES-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlusDIFFERENTIATION-
dc.subject.keywordPlusADIPOCYTES-
dc.subject.keywordPlusMODEL-
dc.subject.keywordPlusDYES-
dc.subject.keywordAuthorLarge Stokes Shift-
dc.subject.keywordAuthorLipophagy-
dc.subject.keywordAuthorLysosomes-
dc.subject.keywordAuthorNear-Infrared-
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