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dc.contributor.authorKomatsu, Naokien
dc.contributor.authorTerai, Kentaen
dc.contributor.authorImanishi, Ayakoen
dc.contributor.authorKamioka, Yujien
dc.contributor.authorSumiyama, Kentaen
dc.contributor.authorJin, Takashien
dc.contributor.authorOkada, Yasushien
dc.contributor.authorNagai, Takeharuen
dc.contributor.authorMatsuda, Michiyukien
dc.contributor.alternative小松, 直貴ja
dc.contributor.alternative寺井, 健太ja
dc.contributor.alternative今西, 彩子ja
dc.contributor.alternative上岡, 裕治ja
dc.contributor.alternative松田, 道行ja
dc.date.accessioned2018-09-21T07:26:13Z-
dc.date.available2018-09-21T07:26:13Z-
dc.date.issued2018-06-12-
dc.identifier.issn2045-2322-
dc.identifier.urihttp://hdl.handle.net/2433/234590-
dc.description.abstractGenetically encoded biosensors based on the principle of Förster resonance energy transfer comprise two major classes: biosensors based on fluorescence resonance energy transfer (FRET) and those based on bioluminescence energy transfer (BRET). The FRET biosensors visualize signaling-molecule activity in cells or tissues with high resolution. Meanwhile, due to the low background signal, the BRET biosensors are primarily used in drug screening. Here, we report a protocol to transform intramolecular FRET biosensors to BRET-FRET hybrid biosensors called hyBRET biosensors. The hyBRET biosensors retain all properties of the prototype FRET biosensors and also work as BRET biosensors with dynamic ranges comparable to the prototype FRET biosensors. The hyBRET biosensors are compatible with optogenetics, luminescence microplate reader assays, and non-invasive whole-body imaging of xenograft and transgenic mice. This simple protocol will expand the use of FRET biosensors and enable visualization of the multiscale dynamics of cell signaling in live animals.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherSpringer Natureen
dc.rights© The Author(s) 2018. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.en
dc.titleA platform of BRET-FRET hybrid biosensors for optogenetics, chemical screening, and in vivo imagingen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleScientific reportsen
dc.identifier.volume8-
dc.relation.doi10.1038/s41598-018-27174-x-
dc.textversionpublisher-
dc.identifier.artnum8984-
dc.addressLaboratory of Bioimaging and Cell Signaling, Graduate School of Biostudies, Kyoto University・Laboratory for Cell Function Dynamics, Center for Brain Science, RIKENen
dc.addressLaboratory of Bioimaging and Cell Signaling, Graduate School of Biostudies, Kyoto Universityen
dc.addressLaboratory of Bioimaging and Cell Signaling, Graduate School of Biostudies, Kyoto Universityen
dc.addressDepartment of Pathology and Biology of Diseases, Graduate School of Medicine, Kyoto University・Department of Molecular Genetics, Institute of Biomedical Science, Kansai Medical Universityen
dc.addressLaboratory for Mouse Genetic Engineering, Quantitative Biology Center, RIKENen
dc.addressLaboratory for Nano-Bio Probes, Quantitative Biology Center, RIKENen
dc.addressLaboratory for Cell Polarity Regulation, Quantitative Biology Center, RIKENen
dc.addressThe Institute of Scientific and Industrial Research, Osaka Universityen
dc.addressLaboratory of Bioimaging and Cell Signaling, Graduate School of Biostudies, Kyoto University・Department of Pathology and Biology of Diseases, Graduate School of Medicine, Kyoto Universityen
dc.identifier.pmid29895862-
dcterms.accessRightsopen access-
datacite.awardNumberJP26890015-
datacite.awardNumber15H02397-
datacite.awardNumber15H0594-
datacite.awardNumber16H06280-
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName日本学術振興会ja
jpcoar.funderName.alternativeJapan Society for the Promotion of Science (JSPS)en
jpcoar.funderName.alternativeJapan Society for the Promotion of Science (JSPS)en
jpcoar.funderName.alternativeJapan Society for the Promotion of Science (JSPS)en
jpcoar.funderName.alternativeJapan Society for the Promotion of Science (JSPS)en
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