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      Optogenetic Control of Bacterial Expression by Red Light

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          Abstract

          In optogenetics, as in nature, sensory photoreceptors serve to control cellular processes by light. Bacteriophytochrome (BphP) photoreceptors sense red and far-red light via a biliverdin chromophore and, in response, cycle between the spectroscopically, structurally, and functionally distinct Pr and Pfr states. BphPs commonly belong to two-component systems that control the phosphorylation of cognate response regulators and downstream gene expression through histidine kinase modules. We recently demonstrated that the paradigm BphP from Deinococcus radiodurans exclusively acts as a phosphatase but that its photosensory module can control the histidine kinase activity of homologous receptors. Here, we apply this insight to reprogram two widely used setups for bacterial gene expression from blue-light to red-light control. The resultant pREDusk and pREDawn systems allow gene expression to be regulated down and up, respectively, uniformly under red light by 100-fold or more. Both setups are realized as portable, single plasmids that encode all necessary components including the biliverdin-producing machinery. The triggering by red light affords high spatial resolution down to the single-cell level. As pREDusk and pREDawn respond sensitively to red light, they support multiplexing with optogenetic systems sensitive to other light colors. Owing to the superior tissue penetration of red light, the pREDawn system can be triggered at therapeutically safe light intensities through material layers, replicating the optical properties of the skin and skull. Given these advantages, pREDusk and pREDawn enable red-light-regulated expression for diverse use cases in bacteria.

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          Two-component signal transduction.

          Most prokaryotic signal-transduction systems and a few eukaryotic pathways use phosphotransfer schemes involving two conserved components, a histidine protein kinase and a response regulator protein. The histidine protein kinase, which is regulated by environmental stimuli, autophosphorylates at a histidine residue, creating a high-energy phosphoryl group that is subsequently transferred to an aspartate residue in the response regulator protein. Phosphorylation induces a conformational change in the regulatory domain that results in activation of an associated domain that effects the response. The basic scheme is highly adaptable, and numerous variations have provided optimization within specific signaling systems. The domains of two-component proteins are modular and can be integrated into proteins and pathways in a variety of ways, but the core structures and activities are maintained. Thus detailed analyses of a relatively small number of representative proteins provide a foundation for understanding this large family of signaling proteins.
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            Millisecond-timescale, genetically targeted optical control of neural activity.

            Temporally precise, noninvasive control of activity in well-defined neuronal populations is a long-sought goal of systems neuroscience. We adapted for this purpose the naturally occurring algal protein Channelrhodopsin-2, a rapidly gated light-sensitive cation channel, by using lentiviral gene delivery in combination with high-speed optical switching to photostimulate mammalian neurons. We demonstrate reliable, millisecond-timescale control of neuronal spiking, as well as control of excitatory and inhibitory synaptic transmission. This technology allows the use of light to alter neural processing at the level of single spikes and synaptic events, yielding a widely applicable tool for neuroscientists and biomedical engineers.
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              A clearer vision for in vivo imaging.

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                Author and article information

                Journal
                ACS Synth Biol
                ACS Synth Biol
                sb
                asbcd6
                ACS Synthetic Biology
                American Chemical Society
                2161-5063
                23 August 2022
                21 October 2022
                : 11
                : 10
                : 3354-3367
                Affiliations
                []Department of Anatomy, University of Helsinki , Helsinki 00014, Finland
                []Lehrstuhl für Biochemie, Photobiochemie, Universität Bayreuth , Bayreuth 95447, Germany
                [§ ]Optoelectronics and Measurement Techniques, University of Oulu , Oulu 90014, Finland
                []Lehrstuhl für Spektroskopie weicher Materie, Universität Bayreuth , Bayreuth 95447, Germany
                []College of Engineering and Physical Sciences, Aston University , Birmingham B4 7ET, U.K.
                [# ]Department of Biological and Environmental Science, Nanoscience Center, University of Jyvaskyla , Jyvaskyla 40014, Finland
                Author notes
                [* ]Email: andreas.moeglich@ 123456uni-bayreuth.de . Phone: +49 921 55 7835.
                [* ]Email: heikki.p.takala@ 123456jyu.fi . Phone: +358 46 923 6211.
                Author information
                https://orcid.org/0000-0002-6447-2803
                https://orcid.org/0000-0002-4214-4008
                https://orcid.org/0000-0002-7382-2772
                https://orcid.org/0000-0003-2518-8583
                Article
                10.1021/acssynbio.2c00259
                9594775
                35998606
                f919dea2-09e9-47a6-a39d-e79293ddf0ca
                © 2022 The Authors. Published by American Chemical Society

                Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 17 May 2022
                Funding
                Funded by: Helsingin Yliopisto, doi 10.13039/100007797;
                Award ID: NA
                Funded by: Academy of Finland, doi 10.13039/501100002341;
                Award ID: 330678
                Funded by: Deutsche Forschungsgemeinschaft, doi 10.13039/501100001659;
                Award ID: MO2192/6-2
                Funded by: European Commission, doi 10.13039/501100000780;
                Award ID: 863214
                Categories
                Research Article
                Custom metadata
                sb2c00259
                sb2c00259

                Molecular biology
                gene expression,optogenetics,phytochrome,sensory photoreceptor,signal transduction,two-component system

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