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dc.contributor.author Mishra, Pratyush Mishra -
dc.contributor.author Kang, Myeong-Gyun -
dc.contributor.author Lee, Hakbong -
dc.contributor.author Kim, Seungjoon -
dc.contributor.author Choi, Subin -
dc.contributor.author Sharma, Nirmali -
dc.contributor.author Park, Cheol-Min -
dc.contributor.author Ko, Jaewon -
dc.contributor.author Lee, Changwook -
dc.contributor.author Seo, Jeong Kon -
dc.contributor.author Rhee, Hyun-Woo -
dc.date.accessioned 2022-01-05T11:00:14Z -
dc.date.available 2022-01-05T11:00:14Z -
dc.date.created 2021-12-16 -
dc.date.issued 2022-01 -
dc.identifier.issn 2041-6520 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/16041 -
dc.description.abstract We developed a proximity photo-crosslinking method (Spotlight) with a 4-azido-N-ethyl-1,8-naphthalimide (AzNP) moiety that can be converted to reactive aryl nitrene species using ambient blue light-emitting diode light. Using an AzNP-conjugated HaloTag ligand (VL1), blue light-induced photo-crosslinked products of various HaloTag-conjugated proteins of interest were detected in subcellular spaces in live cells. Chemical or heat stress-induced dynamic changes in the proteome were also detected, and photo-crosslinking in the mouse brain tissue was enabled. Using Spotlight, we further identified the host interactome of SARS-CoV-2 nucleocapsid (N) protein, which is essential for viral genome assembly. Mass analysis of the VL1-crosslinked product of N-HaloTag in HEK293T cells showed that RNA-binding proteins in stress granules were exclusively enriched in the cross-linked samples. These results tell that our method can reveal the interactome of protein of interest within a short distance in live cells. © 2022 The Royal Society of Chemistry. -
dc.language English -
dc.publisher Royal Society of Chemistry -
dc.title A chemical tool for blue light-inducible proximity photo-crosslinking in live cells -
dc.type Article -
dc.identifier.doi 10.1039/d1sc04871f -
dc.identifier.wosid 000732863800001 -
dc.identifier.scopusid 2-s2.0-85123741409 -
dc.identifier.bibliographicCitation Chemical Science, v.13, no.4, pp.955 - 966 -
dc.description.isOpenAccess TRUE -
dc.subject.keywordPlus HALOTAG7 -
dc.subject.keywordPlus REVEALS -
dc.subject.keywordPlus STAUFEN -
dc.subject.keywordPlus LIGASE -
dc.subject.keywordPlus PROBES -
dc.subject.keywordPlus PROTEIN-PROTEIN INTERACTIONS -
dc.subject.keywordPlus HYDROGEN-SULFIDE -
dc.subject.keywordPlus ARYL AZIDE -
dc.subject.keywordPlus TAG -
dc.subject.keywordPlus BINDING -
dc.citation.endPage 966 -
dc.citation.number 4 -
dc.citation.startPage 955 -
dc.citation.title Chemical Science -
dc.citation.volume 13 -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.relation.journalResearchArea Chemistry -
dc.relation.journalWebOfScienceCategory Chemistry, Multidisciplinary -
dc.type.docType Article -
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Appears in Collections:
Department of Brain Sciences Laboratory of Synapse Formation and Function 1. Journal Articles

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