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Imaging inflammation using an activated macrophage probe with Slc18b1 as the activation-selective gating target

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dc.contributor.authorPark, Sung-Jin-
dc.contributor.authorKim, Beomsue-
dc.contributor.authorChoi, Sejong-
dc.contributor.authorBalasubramaniam, Sivaraman-
dc.contributor.authorLee, Sung-Chan-
dc.contributor.authorLee, Jung Yeol-
dc.contributor.authorKim, Heon Seok-
dc.contributor.authorKim, Jun-Young-
dc.contributor.authorKim, Jong-Jin-
dc.contributor.authorLee, Yong-An-
dc.contributor.authorKang, Nam-Young-
dc.contributor.authorKim, Jin-Soo-
dc.contributor.authorChang, Young-Tae-
dc.date.accessioned2020-04-27T13:03:07Z-
dc.date.available2020-04-27T13:03:07Z-
dc.date.created2020-04-08-
dc.date.created2020-04-08-
dc.date.created2020-04-08-
dc.date.issued2019-12-
dc.identifier.citationNature Communications, Vol.10 No.1, p. 1111-
dc.identifier.issn2041-1723-
dc.identifier.other95256-
dc.identifier.urihttps://hdl.handle.net/10371/165714-
dc.description.abstractActivated macrophages have the potential to be ideal targets for imaging inflammation. However, probe selectivity over non-activated macrophages and probe delivery to target tissue have been challenging. Here, we report a small molecule probe specific for activated macrophages, called CDg16, and demonstrate its application to visualizing inflammatory atherosclerotic plaques in vivo. Through a systematic transporter screen using a CRISPR activation library, we identify the orphan transporter Slc18b1/SLC18B1 as the gating target of CDg16.-
dc.language영어-
dc.publisherNature Publishing Group-
dc.titleImaging inflammation using an activated macrophage probe with Slc18b1 as the activation-selective gating target-
dc.typeArticle-
dc.contributor.AlternativeAuthor김진수-
dc.identifier.doi10.1038/s41467-019-08990-9-
dc.citation.journaltitleNature Communications-
dc.identifier.wosid000460510000008-
dc.identifier.scopusid2-s2.0-85062628220-
dc.citation.number1-
dc.citation.startpage1111-
dc.citation.volume10-
dc.identifier.sci000460510000008-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorKim, Jin-Soo-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusATHEROSCLEROSIS-
dc.subject.keywordPlusTRANSPORT-
dc.subject.keywordPlusDISEASE-
dc.subject.keywordPlusCELLS-
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  • College of Natural Sciences
  • Department of Chemistry
Research Area Biology and Biochemistry

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