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분자분광학및동력학연구단
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Bright ligand-activatable fluorescent protein for high-quality multicolor live-cell super-resolution microscopy

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dc.contributor.authorJiwoong Kwon-
dc.contributor.authorPark, Jong-Seok-
dc.contributor.authorMinsu Kang-
dc.contributor.authorChoi, Soobin-
dc.contributor.authorPark, Jumi-
dc.contributor.authorKim, Gyeong Tae-
dc.contributor.authorLee, Changwook-
dc.contributor.authorCha, Sangwon-
dc.contributor.authorRhee, Hyun-Woo-
dc.contributor.authorSang-Hee Shim-
dc.date.available2020-10-14T08:15:11Z-
dc.date.created2020-02-17-
dc.date.issued2020-01-
dc.identifier.issn2041-1723-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/7254-
dc.description.abstractWe introduce UnaG as a green-to-dark photoswitching fluorescent protein capable of high-quality super-resolution imaging with photon numbers equivalent to the brightest photoswitchable red protein. UnaG only fluoresces upon binding of a fluorogenic metabolite, bilirubin, enabling UV-free reversible photoswitching with easily controllable kinetics and low background under Epi illumination. The on- and off-switching rates are controlled by the concentration of the ligand and the excitation light intensity, respectively, where the dissolved oxygen also promotes the off-switching. The photo-oxidation reaction mechanism of bilirubin in UnaG suggests that the lack of ligand-protein covalent bond allows the oxidized ligand to detach from the protein, emptying the binding cavity for rebinding to a fresh ligand molecule. We demonstrate super-resolution single-molecule localization imaging of various subcellular structures genetically encoded with UnaG, which enables facile labeling and simultaneous multicolor imaging of live cells. UnaG has the promise of becoming a default protein for high-performance super-resolution imaging. © The Author(s) 2020-
dc.description.uri1-
dc.language영어-
dc.publisherNATURE PUBLISHING GROUP-
dc.subjectBiological techniques, Biophysical methods, Biophysics, Imaging, Microscopy-
dc.titleBright ligand-activatable fluorescent protein for high-quality multicolor live-cell super-resolution microscopy-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000528906000005-
dc.identifier.scopusid2-s2.0-85077874510-
dc.identifier.rimsid71198-
dc.contributor.affiliatedAuthorJiwoong Kwon-
dc.contributor.affiliatedAuthorMinsu Kang-
dc.contributor.affiliatedAuthorSang-Hee Shim-
dc.identifier.doi10.1038/s41467-019-14067-4-
dc.identifier.bibliographicCitationNATURE COMMUNICATIONS, v.11, no.1, pp.273-
dc.citation.titleNATURE COMMUNICATIONS-
dc.citation.volume11-
dc.citation.number1-
dc.citation.startPage273-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.subject.keywordPlusBILIRUBIN-
dc.subject.keywordPlusMOLECULES-
dc.subject.keywordPlusMECHANISM-
dc.subject.keywordPlusCYTOCHROME-P450-
dc.subject.keywordPlusDEGRADATION-
dc.subject.keywordPlusPERFORMANCE-
dc.subject.keywordPlusREPORTER-
dc.subject.keywordPlusPRODUCTS-
dc.subject.keywordPlusBINDING-
dc.subject.keywordPlusTAG-
Appears in Collections:
Center for Molecular Spectroscopy and Dynamics(분자 분광학 및 동력학 연구단) > 1. Journal Papers (저널논문)
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