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

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          Abstract

          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 ( 1O 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 1O 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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          Photodynamic therapy (PDT): a short review on cellular mechanisms and cancer research applications for PDT.

          Photodynamic therapy (PDT) has been used for many years, but it is only now becoming widely accepted and utilized. Originally it was developed as a tumor therapy and some of its most successful applications are for non-malignant diseases. This article provides a broad review of different parameters used and mechanisms instituted in PDT such as photosensitizers (PS), photochemistry and photophysics, cellular localization, cellular signaling, cell metabolism and modes of cell death that operate on a cellular level, as well as photosensitizer pharmacokinetics, biodistribution, tumor localization and modes of tumor destruction. These specific cellular mechanisms are most commonly applied in PDT and for the most part are often researched and exploited. If the combination of these specific parameters and mechanisms can be optimized within PDT it could possibly be used as a suitable alternative for the treatment and management of specific cancers.
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            Bright monomeric red fluorescent protein with an extended fluorescence lifetime.

            Fluorescent proteins have become extremely popular tools for in vivo imaging and especially for the study of localization, motility and interaction of proteins in living cells. Here we report TagRFP, a monomeric red fluorescent protein, which is characterized by high brightness, complete chromophore maturation, prolonged fluorescence lifetime and high pH-stability. These properties make TagRFP an excellent tag for protein localization studies and fluorescence resonance energy transfer (FRET) applications.
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              DNA microarray-mediated transcriptional profiling of the Escherichia coli response to hydrogen peroxide.

              The genome-wide transcription profile of Escherichia coli cells treated with hydrogen peroxide was examined with a DNA microarray composed of 4,169 E. coli open reading frames. By measuring gene expression in isogenic wild-type and oxyR deletion strains, we confirmed that the peroxide response regulator OxyR activates most of the highly hydrogen peroxide-inducible genes. The DNA microarray measurements allowed the identification of several new OxyR-activated genes, including the hemH heme biosynthetic gene; the six-gene suf operon, which may participate in Fe-S cluster assembly or repair; and four genes of unknown function. We also identified several genes, including uxuA, encoding mannonate hydrolase, whose expression might be repressed by OxyR, since their expression was elevated in the DeltaoxyR mutant strain. In addition, the induction of some genes was found to be OxyR independent, indicating the existence of other peroxide sensors and regulators in E. coli. For example, the isc operon, which specifies Fe-S cluster formation and repair activities, was induced by hydrogen peroxide in strains lacking either OxyR or the superoxide response regulators SoxRS. These results expand our understanding of the oxidative stress response and raise interesting questions regarding the nature of other regulators that modulate gene expression in response to hydrogen peroxide.
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                Author and article information

                Contributors
                santi.nonell@iqs.url.edu
                t.drepper@fz-juelich.de
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                9 October 2018
                9 October 2018
                2018
                : 8
                : 15021
                Affiliations
                [1 ]ISNI 0000 0001 2297 375X, GRID grid.8385.6, Institute of Molecular Enzyme Technology, Heinrich-Heine-University Düsseldorf, Forschungszentrum Jülich GmbH, ; Jülich, Germany
                [2 ]m2p-labs GmbH, Baesweiler, Germany
                [3 ]Institut Químic de Sarrià, Universitat Ramon Llull, Barcelona, Spain
                [4 ]ISNI 0000 0001 2297 375X, GRID grid.8385.6, Institute of Bio- and Geosciences, IBG-1: Biotechnology, Forschungszentrum Jülich GmbH, ; Jülich, Germany
                [5 ]ISNI 0000 0001 2097 3940, GRID grid.9499.d, Instituto de Investigaciones Teóricas y Aplicadas, Universidad Nacional de La Plata, ; La Plata, Argentina
                [6 ]ISNI 0000 0001 2297 375X, GRID grid.8385.6, Institute of Complex Systems, ICS-4: Cellular Biophysics, Forschungszentrum Jülich GmbH, ; Jülich, Germany
                Author information
                http://orcid.org/0000-0001-7279-264X
                http://orcid.org/0000-0002-3903-4705
                http://orcid.org/0000-0002-8900-5291
                http://orcid.org/0000-0002-0096-8084
                Article
                33291
                10.1038/s41598-018-33291-4
                6177443
                30301917
                45c4fbfc-17f8-4f42-a8b3-e69f86bf157f
                © 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/.

                History
                : 29 December 2017
                : 26 September 2018
                Funding
                Funded by: FundRef https://doi.org/10.13039/501100002347, Bundesministerium für Bildung und Forschung (Federal Ministry of Education and Research);
                Award ID: FKZ 031A16
                Award ID: FKZ 031A16
                Award Recipient :
                Funded by: FundRef https://doi.org/10.13039/100008666, Fundació la Marató de TV3;
                Award ID: 20133133
                Award Recipient :
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