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Chromophore Renewal and Fluorogen-Binding Tags: A Match Made to Last
Fluorogen-binding tags, which activate the fluorescence of a specific chromophore (so-called fluorogen) upon reversible binding, have recently been proposed as a way of reducing photobleaching via fluorogen renewal. However, no generic methodology has been proposed to systematically analyze the phot...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5615068/ https://www.ncbi.nlm.nih.gov/pubmed/28951577 http://dx.doi.org/10.1038/s41598-017-12400-9 |
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author | Pimenta, Frederico M. Chiappetta, Giovanni Le Saux, Thomas Vinh, Joëlle Jullien, Ludovic Gautier, Arnaud |
author_facet | Pimenta, Frederico M. Chiappetta, Giovanni Le Saux, Thomas Vinh, Joëlle Jullien, Ludovic Gautier, Arnaud |
author_sort | Pimenta, Frederico M. |
collection | PubMed |
description | Fluorogen-binding tags, which activate the fluorescence of a specific chromophore (so-called fluorogen) upon reversible binding, have recently been proposed as a way of reducing photobleaching via fluorogen renewal. However, no generic methodology has been proposed to systematically analyze the photodamage of the fluorogen and the protein tag. Using Y-FAST (Yellow Fluorescence-activating and Absorption-Shifting Tag) as a case study we propose here a generic experimental and theoretical approach to assess how fluorogen renewal reduces the apparent photobleaching rate of a fluorogen-binding tag. Y-FAST has its apparent photobleaching rate greatly reduced by fluorogen renewal and its photostability is mainly limited by oxidation of specific residues in the protein scaffold by reactive oxygen species generated by the bound fluorogen. This study sets the groundwork for the optimization of fluorogenic systems, helping guide rational improvements to their photostability. |
format | Online Article Text |
id | pubmed-5615068 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-56150682017-10-11 Chromophore Renewal and Fluorogen-Binding Tags: A Match Made to Last Pimenta, Frederico M. Chiappetta, Giovanni Le Saux, Thomas Vinh, Joëlle Jullien, Ludovic Gautier, Arnaud Sci Rep Article Fluorogen-binding tags, which activate the fluorescence of a specific chromophore (so-called fluorogen) upon reversible binding, have recently been proposed as a way of reducing photobleaching via fluorogen renewal. However, no generic methodology has been proposed to systematically analyze the photodamage of the fluorogen and the protein tag. Using Y-FAST (Yellow Fluorescence-activating and Absorption-Shifting Tag) as a case study we propose here a generic experimental and theoretical approach to assess how fluorogen renewal reduces the apparent photobleaching rate of a fluorogen-binding tag. Y-FAST has its apparent photobleaching rate greatly reduced by fluorogen renewal and its photostability is mainly limited by oxidation of specific residues in the protein scaffold by reactive oxygen species generated by the bound fluorogen. This study sets the groundwork for the optimization of fluorogenic systems, helping guide rational improvements to their photostability. Nature Publishing Group UK 2017-09-26 /pmc/articles/PMC5615068/ /pubmed/28951577 http://dx.doi.org/10.1038/s41598-017-12400-9 Text en © The Author(s) 2017 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 Pimenta, Frederico M. Chiappetta, Giovanni Le Saux, Thomas Vinh, Joëlle Jullien, Ludovic Gautier, Arnaud Chromophore Renewal and Fluorogen-Binding Tags: A Match Made to Last |
title | Chromophore Renewal and Fluorogen-Binding Tags: A Match Made to Last |
title_full | Chromophore Renewal and Fluorogen-Binding Tags: A Match Made to Last |
title_fullStr | Chromophore Renewal and Fluorogen-Binding Tags: A Match Made to Last |
title_full_unstemmed | Chromophore Renewal and Fluorogen-Binding Tags: A Match Made to Last |
title_short | Chromophore Renewal and Fluorogen-Binding Tags: A Match Made to Last |
title_sort | chromophore renewal and fluorogen-binding tags: a match made to last |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5615068/ https://www.ncbi.nlm.nih.gov/pubmed/28951577 http://dx.doi.org/10.1038/s41598-017-12400-9 |
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