Optogenetic oligomerization of Rab GTPases regulates intracellular membrane trafficking

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dc.contributor.authorNguyen, Mai Khanhko
dc.contributor.authorKim, Cha Yeonko
dc.contributor.authorKim, Jin Manko
dc.contributor.authorPark, Byung Oukko
dc.contributor.authorLee, Sangkyuko
dc.contributor.authorPark, Hyerimko
dc.contributor.authorHeo, Won Doko
dc.date.accessioned2016-07-06T04:18:47Z-
dc.date.available2016-07-06T04:18:47Z-
dc.date.created2016-06-08-
dc.date.created2016-06-08-
dc.date.created2016-06-08-
dc.date.issued2016-06-
dc.identifier.citationNATURE CHEMICAL BIOLOGY, v.12, no.6, pp.431 - U86-
dc.identifier.issn1552-4450-
dc.identifier.urihttp://hdl.handle.net/10203/209475-
dc.description.abstractIntracellular membrane trafficking, which is involved in diverse cellular processes, is dynamic and difficult to study in a spatiotemporal manner. Here we report an optogenetic strategy, termed light-activated reversible inhibition by assembled trap of intracellular membranes (IM-LARIAT), that uses various Rab GTPases combined with blue-light-induced hetero-interaction between cryptochrome 2 and CIB1. In this system, illumination induces a rapid and reversible intracellular membrane aggregation that disrupts the dynamics and functions of the targeted membrane. We applied IM-LARIAT to specifically perturb several Rab-mediated trafficking processes, including receptor transport, protein sorting and secretion, and signaling initiated from endosomes. We finally used this tool to reveal different functions of local Rab5-mediated and Rab11-mediated membrane trafficking in growth cones and soma of young hippocampal neurons. Our results show that IM-LARIAT is a versatile tool that can be used to dissect spatiotemporal functions of intracellular membranes in diverse systems-
dc.languageEnglish-
dc.publisherNATURE PUBLISHING GROUP-
dc.titleOptogenetic oligomerization of Rab GTPases regulates intracellular membrane trafficking-
dc.typeArticle-
dc.identifier.wosid000376160600013-
dc.identifier.scopusid2-s2.0-84970027518-
dc.type.rimsART-
dc.citation.volume12-
dc.citation.issue6-
dc.citation.beginningpage431-
dc.citation.endingpageU86-
dc.citation.publicationnameNATURE CHEMICAL BIOLOGY-
dc.identifier.doi10.1038/NCHEMBIO.2064-
dc.contributor.localauthorHeo, Won Do-
dc.contributor.nonIdAuthorPark, Byung Ouk-
dc.contributor.nonIdAuthorLee, Sangkyu-
dc.type.journalArticleArticle-
dc.subject.keywordPlusGROWTH-FACTOR-
dc.subject.keywordPlusENDOCYTIC TRAFFICKING-
dc.subject.keywordPlusTRANSFERRIN RECEPTOR-
dc.subject.keywordPlusLIVING CELLS-
dc.subject.keywordPlusAXON GROWTH-
dc.subject.keywordPlusPC12 CELLS-
dc.subject.keywordPlusBLUE-LIGHT-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusTRANSPORT-
dc.subject.keywordPlusENDOSOME-
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