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      Structure-guided design and functional characterization of an artificial red light–regulated guanylate/adenylate cyclase for optogenetic applications

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          Abstract

          Genetically targeting biological systems to control cellular processes with light is the concept of optogenetics. Despite impressive developments in this field, underlying molecular mechanisms of signal transduction of the employed photoreceptor modules are frequently not sufficiently understood to rationally design new optogenetic tools. Here, we investigate the requirements for functional coupling of red light–sensing phytochromes with non-natural enzymatic effectors by creating a series of constructs featuring the Deinococcus radiodurans bacteriophytochrome linked to a Synechocystis guanylate/adenylate cyclase. Incorporating characteristic structural elements important for cyclase regulation in our designs, we identified several red light–regulated fusions with promising properties. We provide details of one light-activated construct with low dark-state activity and high dynamic range that outperforms previous optogenetic tools in vitro and expands our in vivo toolkit, as demonstrated by manipulation of Caenorhabditis elegans locomotor activity. The full-length crystal structure of this phytochrome-linked cyclase revealed molecular details of photoreceptor–effector coupling, highlighting the importance of the regulatory cyclase element. Analysis of conformational dynamics by hydrogen–deuterium exchange in different functional states enriched our understanding of phytochrome signaling and signal integration by effectors. We found that light-induced conformational changes in the phytochrome destabilize the coiled-coil sensor–effector linker, which releases the cyclase regulatory element from an inhibited conformation, increasing cyclase activity of this artificial system. Future designs of optogenetic functionalities may benefit from our work, indicating that rational considerations for the effector improve the rate of success of initial designs to obtain optogenetic tools with superior properties.

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          Most cited references37

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          Efficient gene transfer in C.elegans: extrachromosomal maintenance and integration of transforming sequences.

          We describe a dominant behavioral marker, rol-6(su-1006), and an efficient microinjection procedure which facilitate the recovery of Caenorhabditis elegans transformants. We use these tools to study the mechanism of C.elegans DNA transformation. By injecting mixtures of genetically marked DNA molecules, we show that large extrachromosomal arrays assemble directly from the injected molecules and that homologous recombination drives array assembly. Appropriately placed double-strand breaks stimulated homologous recombination during array formation. Our data indicate that the size of the assembled transgenic structures determines whether or not they will be maintained extrachromosomally or lost. We show that low copy number extrachromosomal transformation can be achieved by adjusting the relative concentration of DNA molecules in the injection mixture. Integration of the injected DNA, though relatively rare, was reproducibly achieved when single-stranded oligonucleotide was co-injected with the double-stranded DNA.
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            Optimal description of a protein structure in terms of multiple groups undergoing TLS motion.

            A single protein crystal structure contains information about dynamic properties of the protein as well as providing a static view of one three-dimensional conformation. This additional information is to be found in the distribution of observed electron density about the mean position of each atom. It is general practice to account for this by refining a separate atomic displacement parameter (ADP) for each atomic center. However, these same displacements are often described well by simpler models based on TLS (translation/libration/screw) rigid-body motion of large groups of atoms, for example interdomain hinge motion. A procedure, TLSMD, has been developed that analyzes the distribution of ADPs in a previously refined protein crystal structure in order to generate optimal multi-group TLS descriptions of the constituent protein chains. TLSMD is applicable to crystal structures at any resolution. The models generated by TLSMD analysis can significantly improve the standard crystallographic residuals R and R(free) and can reveal intrinsic dynamic properties of the protein.
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              Ectopic expression of a microbial-type rhodopsin restores visual responses in mice with photoreceptor degeneration.

              The death of photoreceptor cells caused by retinal degenerative diseases often results in a complete loss of retinal responses to light. We explore the feasibility of converting inner retinal neurons to photosensitive cells as a possible strategy for imparting light sensitivity to retinas lacking rods and cones. Using delivery by an adeno-associated viral vector, here, we show that long-term expression of a microbial-type rhodopsin, channelrhodopsin-2 (ChR2), can be achieved in rodent inner retinal neurons in vivo. Furthermore, we demonstrate that expression of ChR2 in surviving inner retinal neurons of a mouse with photoreceptor degeneration can restore the ability of the retina to encode light signals and transmit the light signals to the visual cortex. Thus, expression of microbial-type channelrhodopsins, such as ChR2, in surviving inner retinal neurons is a potential strategy for the restoration of vision after rod and cone degeneration.
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                Author and article information

                Journal
                J Biol Chem
                J. Biol. Chem
                jbc
                jbc
                JBC
                The Journal of Biological Chemistry
                American Society for Biochemistry and Molecular Biology (11200 Rockville Pike, Suite 302, Rockville, MD 20852-3110, U.S.A. )
                0021-9258
                1083-351X
                8 June 2018
                25 April 2018
                25 April 2018
                : 293
                : 23
                : 9078-9089
                Affiliations
                From the []Institute of Biochemistry, Graz University of Technology, Petersgasse 12/II, 8010 Graz, Austria,
                the [§ ]Max Planck Institute for Medical Research, Jahnstrasse 29, Heidelberg 69120, Germany, and
                the []Department of Biology, Saint Joseph's University, Philadelphia, Pennsylvania 19131
                Author notes
                [3 ] To whom correspondence should be addressed. E-mail: Andreas.Winkler@ 123456TUGraz.at .
                [1]

                Supported by the Austrian Science Fund Ph.D. program “DK Molecular Enzymology” Grant W901.

                [2]

                Supported by the NIGMS National Institutes of Health Grant R15GM122058.

                Edited by F. Peter Guengerich

                Author information
                https://orcid.org/0000-0002-2085-8974
                https://orcid.org/0000-0001-6221-9671
                Article
                RA118.003069
                10.1074/jbc.RA118.003069
                5995499
                29695503
                de1b4b75-7612-4abf-aba9-366a9dcb95cb
                © 2018 Etzl et al.

                Published under exclusive license by The American Society for Biochemistry and Molecular Biology, Inc.

                Author's Choice—Final version free via Creative Commons CC-BY license.

                History
                : 21 March 2018
                : 21 April 2018
                Funding
                Funded by: Austrian Science Fund (FWF) , open-funder-registry 10.13039/501100002428;
                Award ID: P27124
                Funded by: HHS | NIH | National Institute of General Medical Sciences (NIGMS) , open-funder-registry 10.13039/100000057;
                Award ID: R15GM122058
                Categories
                Protein Structure and Folding

                Biochemistry
                adenylate cyclase (adenylyl cyclase),guanylate cyclase (guanylyl cyclase),photoreceptor,optogenetics,hydrogen-deuterium exchange,allosteric regulation,adenylyl cyclase,bacteriophytochrome,light regulation,photosensor

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