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An optogenetic toolbox of LOV-based photosensitizers for light-driven killing of bacteria

Flavin-binding fluorescent proteins (FPs) are genetically encoded in vivo reporters, which are derived from microbial and plant LOV photoreceptors. In this study, we comparatively analyzed ROS formation and light-driven antimicrobial efficacy of eleven LOV-based FPs. In particular, we determined sin...

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Autores principales: Endres, Stephan, Wingen, Marcus, Torra, Joaquim, Ruiz-González, Rubén, Polen, Tino, Bosio, Gabriela, Bitzenhofer, Nora Lisa, Hilgers, Fabienne, Gensch, Thomas, Nonell, Santi, Jaeger, Karl-Erich, Drepper, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6177443/
https://www.ncbi.nlm.nih.gov/pubmed/30301917
http://dx.doi.org/10.1038/s41598-018-33291-4
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author Endres, Stephan
Wingen, Marcus
Torra, Joaquim
Ruiz-González, Rubén
Polen, Tino
Bosio, Gabriela
Bitzenhofer, Nora Lisa
Hilgers, Fabienne
Gensch, Thomas
Nonell, Santi
Jaeger, Karl-Erich
Drepper, Thomas
author_facet Endres, Stephan
Wingen, Marcus
Torra, Joaquim
Ruiz-González, Rubén
Polen, Tino
Bosio, Gabriela
Bitzenhofer, Nora Lisa
Hilgers, Fabienne
Gensch, Thomas
Nonell, Santi
Jaeger, Karl-Erich
Drepper, Thomas
author_sort Endres, Stephan
collection PubMed
description Flavin-binding fluorescent proteins (FPs) are genetically encoded in vivo reporters, which are derived from microbial and plant LOV photoreceptors. In this study, we comparatively analyzed ROS formation and light-driven antimicrobial efficacy of eleven LOV-based FPs. In particular, we determined singlet oxygen ((1)O(2)) quantum yields and superoxide photosensitization activities via spectroscopic assays and performed cell toxicity experiments in E. coli. Besides miniSOG and SOPP, which have been engineered to generate (1)O(2), all of the other tested flavoproteins were able to produce singlet oxygen and/or hydrogen peroxide but exhibited remarkable differences in ROS selectivity and yield. Accordingly, most LOV-FPs are potent photosensitizers, which can be used for light-controlled killing of bacteria. Furthermore, the two variants Pp2FbFP and DsFbFP M49I, exhibiting preferential photosensitization of singlet oxygen or singlet oxygen and superoxide, respectively, were shown to be new tools for studying specific ROS-induced cell signaling processes. The tested LOV-FPs thus further expand the toolbox of optogenetic sensitizers usable for a broad spectrum of microbiological and biomedical applications.
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spelling pubmed-61774432018-10-12 An optogenetic toolbox of LOV-based photosensitizers for light-driven killing of bacteria Endres, Stephan Wingen, Marcus Torra, Joaquim Ruiz-González, Rubén Polen, Tino Bosio, Gabriela Bitzenhofer, Nora Lisa Hilgers, Fabienne Gensch, Thomas Nonell, Santi Jaeger, Karl-Erich Drepper, Thomas Sci Rep Article Flavin-binding fluorescent proteins (FPs) are genetically encoded in vivo reporters, which are derived from microbial and plant LOV photoreceptors. In this study, we comparatively analyzed ROS formation and light-driven antimicrobial efficacy of eleven LOV-based FPs. In particular, we determined singlet oxygen ((1)O(2)) quantum yields and superoxide photosensitization activities via spectroscopic assays and performed cell toxicity experiments in E. coli. Besides miniSOG and SOPP, which have been engineered to generate (1)O(2), all of the other tested flavoproteins were able to produce singlet oxygen and/or hydrogen peroxide but exhibited remarkable differences in ROS selectivity and yield. Accordingly, most LOV-FPs are potent photosensitizers, which can be used for light-controlled killing of bacteria. Furthermore, the two variants Pp2FbFP and DsFbFP M49I, exhibiting preferential photosensitization of singlet oxygen or singlet oxygen and superoxide, respectively, were shown to be new tools for studying specific ROS-induced cell signaling processes. The tested LOV-FPs thus further expand the toolbox of optogenetic sensitizers usable for a broad spectrum of microbiological and biomedical applications. Nature Publishing Group UK 2018-10-09 /pmc/articles/PMC6177443/ /pubmed/30301917 http://dx.doi.org/10.1038/s41598-018-33291-4 Text en © The Author(s) 2018 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
Endres, Stephan
Wingen, Marcus
Torra, Joaquim
Ruiz-González, Rubén
Polen, Tino
Bosio, Gabriela
Bitzenhofer, Nora Lisa
Hilgers, Fabienne
Gensch, Thomas
Nonell, Santi
Jaeger, Karl-Erich
Drepper, Thomas
An optogenetic toolbox of LOV-based photosensitizers for light-driven killing of bacteria
title An optogenetic toolbox of LOV-based photosensitizers for light-driven killing of bacteria
title_full An optogenetic toolbox of LOV-based photosensitizers for light-driven killing of bacteria
title_fullStr An optogenetic toolbox of LOV-based photosensitizers for light-driven killing of bacteria
title_full_unstemmed An optogenetic toolbox of LOV-based photosensitizers for light-driven killing of bacteria
title_short An optogenetic toolbox of LOV-based photosensitizers for light-driven killing of bacteria
title_sort optogenetic toolbox of lov-based photosensitizers for light-driven killing of bacteria
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6177443/
https://www.ncbi.nlm.nih.gov/pubmed/30301917
http://dx.doi.org/10.1038/s41598-018-33291-4
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