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

We 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...

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Autores principales: Kwon, Jiwoong, Park, Jong-Seok, Kang, Minsu, Choi, Soobin, Park, Jumi, Kim, Gyeong Tae, Lee, Changwook, Cha, Sangwon, Rhee, Hyun-Woo, Shim, Sang-Hee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6959352/
https://www.ncbi.nlm.nih.gov/pubmed/31937765
http://dx.doi.org/10.1038/s41467-019-14067-4
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author Kwon, Jiwoong
Park, Jong-Seok
Kang, Minsu
Choi, Soobin
Park, Jumi
Kim, Gyeong Tae
Lee, Changwook
Cha, Sangwon
Rhee, Hyun-Woo
Shim, Sang-Hee
author_facet Kwon, Jiwoong
Park, Jong-Seok
Kang, Minsu
Choi, Soobin
Park, Jumi
Kim, Gyeong Tae
Lee, Changwook
Cha, Sangwon
Rhee, Hyun-Woo
Shim, Sang-Hee
author_sort Kwon, Jiwoong
collection PubMed
description We 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.
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spelling pubmed-69593522020-01-15 Bright ligand-activatable fluorescent protein for high-quality multicolor live-cell super-resolution microscopy Kwon, Jiwoong Park, Jong-Seok Kang, Minsu Choi, Soobin Park, Jumi Kim, Gyeong Tae Lee, Changwook Cha, Sangwon Rhee, Hyun-Woo Shim, Sang-Hee Nat Commun Article We 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. Nature Publishing Group UK 2020-01-14 /pmc/articles/PMC6959352/ /pubmed/31937765 http://dx.doi.org/10.1038/s41467-019-14067-4 Text en © The Author(s) 2020 Open Access 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/.
spellingShingle Article
Kwon, Jiwoong
Park, Jong-Seok
Kang, Minsu
Choi, Soobin
Park, Jumi
Kim, Gyeong Tae
Lee, Changwook
Cha, Sangwon
Rhee, Hyun-Woo
Shim, Sang-Hee
Bright ligand-activatable fluorescent protein for high-quality multicolor live-cell super-resolution microscopy
title Bright ligand-activatable fluorescent protein for high-quality multicolor live-cell super-resolution microscopy
title_full Bright ligand-activatable fluorescent protein for high-quality multicolor live-cell super-resolution microscopy
title_fullStr Bright ligand-activatable fluorescent protein for high-quality multicolor live-cell super-resolution microscopy
title_full_unstemmed Bright ligand-activatable fluorescent protein for high-quality multicolor live-cell super-resolution microscopy
title_short Bright ligand-activatable fluorescent protein for high-quality multicolor live-cell super-resolution microscopy
title_sort bright ligand-activatable fluorescent protein for high-quality multicolor live-cell super-resolution microscopy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6959352/
https://www.ncbi.nlm.nih.gov/pubmed/31937765
http://dx.doi.org/10.1038/s41467-019-14067-4
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