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복잡계자기조립연구단
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Visualizing Microglia with a Fluorescence Turn-On Ugt1a7c Substrate

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dc.contributor.authorBeomsue Kim-
dc.contributor.authorMasahiro Fukuda-
dc.contributor.authorJung-Yeol Lee-
dc.contributor.authorDongdong Su-
dc.contributor.authorSrikanta Sanu-
dc.contributor.authorAymeric Silvin-
dc.contributor.authorAudrey T. T. Khoo-
dc.contributor.authorTaejoon Kwon-
dc.contributor.authorXiao Liu-
dc.contributor.authorWeijie Chi-
dc.contributor.authorXiaogang Liu-
dc.contributor.authorSejong Choi-
dc.contributor.authorDiana S. Y. Wan-
dc.contributor.authorSung-Jin Park-
dc.contributor.authorJin Soo Kim-
dc.contributor.authorFlorent Ginhoux-
dc.contributor.authorH. Shawn Je-
dc.contributor.authorYoung Tae Chang-
dc.date.available2019-08-21T06:20:28Z-
dc.date.created2019-05-29-
dc.date.issued2019-06-
dc.identifier.issn1433-7851-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/6068-
dc.description.abstract© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim Microglia, the brain-resident macrophage, are involved in brain development and contribute to the progression of neural disorders. Despite the importance of microglia, imaging of live microglia at a cellular resolution has been limited to transgenic mice. Efforts have therefore been dedicated to developing new methods for microglia detection and imaging. Using a thorough structure–activity relationships study, we developed CDr20, a high-performance fluorogenic chemical probe that enables the visualization of microglia both in vitro and in vivo. Using a genome-scale CRISPR-Cas9 knockout screen, the UDP-glucuronosyltransferase Ugt1a7c was identified as the target of CDr20. The glucuronidation of CDr20 by Ugt1a7c in microglia produces fluorescence-
dc.description.uri1-
dc.language영어-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.subjectbiological activity-
dc.subjectfluorescent probes-
dc.subjectimaging agents-
dc.subjectmicroglia-
dc.subjectstructure–activity relationships-
dc.titleVisualizing Microglia with a Fluorescence Turn-On Ugt1a7c Substrate-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000474117600005-
dc.identifier.scopusid2-s2.0-85065170767-
dc.identifier.rimsid68279-
dc.contributor.affiliatedAuthorXiao Liu-
dc.contributor.affiliatedAuthorJin Soo Kim-
dc.contributor.affiliatedAuthorYoung Tae Chang-
dc.identifier.doi10.1002/anie.201903058-
dc.identifier.bibliographicCitationANGEWANDTE CHEMIE-INTERNATIONAL EDITION, v.58, no.24, pp.7972 - 7976-
dc.citation.titleANGEWANDTE CHEMIE-INTERNATIONAL EDITION-
dc.citation.volume58-
dc.citation.number24-
dc.citation.startPage7972-
dc.citation.endPage7976-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlusTRANSCRIPTOME-
dc.subject.keywordAuthorbiological activity-
dc.subject.keywordAuthorfluorescent probes-
dc.subject.keywordAuthorimaging agents-
dc.subject.keywordAuthormicroglia-
dc.subject.keywordAuthorstructure-activity relationships-
Appears in Collections:
Center for Self-assembly and Complexity(복잡계 자기조립 연구단) > 1. Journal Papers (저널논문)
Center for Genome Engineering(유전체 교정 연구단) > 1. Journal Papers (저널논문)
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