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      Designs, applications, and limitations of genetically encoded fluorescent sensors to explore plant biology

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          Abstract

          The understanding of signaling and metabolic processes in multicellular organisms requires knowledge of the spatial dynamics of small molecules and the activities of enzymes, transporters, and other proteins in vivo, as well as biophysical parameters inside cells and across tissues. The cellular distribution of receptors, ligands, and activation state must be integrated with information about the cellular distribution of metabolites in relation to metabolic fluxes and signaling dynamics in order to achieve the promise of in vivo biochemistry. Genetically encoded sensors are engineered fluorescent proteins that have been developed for a wide range of small molecules, such as ions and metabolites, or to report biophysical processes, such as transmembrane voltage or tension. First steps have been taken to monitor the activity of transporters in vivo. Advancements in imaging technologies and specimen handling and stimulation have enabled researchers in plant sciences to implement sensor technologies in intact plants. Here, we provide a brief history of the development of genetically encoded sensors and an overview of the types of sensors available for quantifying and visualizing ion and metabolite distribution and dynamics. We further discuss the pros and cons of specific sensor designs, imaging systems, and sample manipulations, provide advice on the choice of technology, and give an outlook into future developments.

          Abstract

          Different types of genetically encoded sensors in plants can be used to quantify and visualize ion and metabolite distributions and dynamics.

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          Most cited references191

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          The green fluorescent protein.

          R Tsien (1998)
          In just three years, the green fluorescent protein (GFP) from the jellyfish Aequorea victoria has vaulted from obscurity to become one of the most widely studied and exploited proteins in biochemistry and cell biology. Its amazing ability to generate a highly visible, efficiently emitting internal fluorophore is both intrinsically fascinating and tremendously valuable. High-resolution crystal structures of GFP offer unprecedented opportunities to understand and manipulate the relation between protein structure and spectroscopic function. GFP has become well established as a marker of gene expression and protein targeting in intact cells and organisms. Mutagenesis and engineering of GFP into chimeric proteins are opening new vistas in physiological indicators, biosensors, and photochemical memories.
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            Fluorescent indicators for Ca2+ based on green fluorescent proteins and calmodulin.

            Important Ca2+ signals in the cytosol and organelles are often extremely localized and hard to measure. To overcome this problem we have constructed new fluorescent indicators for Ca2+ that are genetically encoded without cofactors and are targetable to specific intracellular locations. We have dubbed these fluorescent indicators 'cameleons'. They consist of tandem fusions of a blue- or cyan-emitting mutant of the green fluorescent protein (GFP), calmodulin, the calmodulin-binding peptide M13, and an enhanced green- or yellow-emitting GFP. Binding of Ca2+ makes calmodulin wrap around the M13 domain, increasing the fluorescence resonance energy transfer (FRET) between the flanking GFPs. Calmodulin mutations can tune the Ca2+ affinities to measure free Ca2+ concentrations in the range 10(-8) to 10(-2) M. We have visualized free Ca2+ dynamics in the cytosol, nucleus and endoplasmic reticulum of single HeLa cells transfected with complementary DNAs encoding chimaeras bearing appropriate localization signals. Ca2+ concentration in the endoplasmic reticulum of individual cells ranged from 60 to 400 microM at rest, and 1 to 50 microM after Ca2+ mobilization. FRET is also an indicator of the reversible intermolecular association of cyan-GFP-labelled calmodulin with yellow-GFP-labelled M13. Thus FRET between GFP mutants can monitor localized Ca2+ signals and protein heterodimerization in individual live cells.
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              Sugar transporters for intercellular exchange and nutrition of pathogens.

              Sugar efflux transporters are essential for the maintenance of animal blood glucose levels, plant nectar production, and plant seed and pollen development. Despite broad biological importance, the identity of sugar efflux transporters has remained elusive. Using optical glucose sensors, we identified a new class of sugar transporters, named SWEETs, and show that at least six out of seventeen Arabidopsis, two out of over twenty rice and two out of seven homologues in Caenorhabditis elegans, and the single copy human protein, mediate glucose transport. Arabidopsis SWEET8 is essential for pollen viability, and the rice homologues SWEET11 and SWEET14 are specifically exploited by bacterial pathogens for virulence by means of direct binding of a bacterial effector to the SWEET promoter. Bacterial symbionts and fungal and bacterial pathogens induce the expression of different SWEET genes, indicating that the sugar efflux function of SWEET transporters is probably targeted by pathogens and symbionts for nutritional gain. The metazoan homologues may be involved in sugar efflux from intestinal, liver, epididymis and mammary cells.
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                Author and article information

                Journal
                Plant Physiol
                Plant Physiol
                plphys
                Plant Physiology
                Oxford University Press
                0032-0889
                1532-2548
                October 2021
                30 August 2021
                30 August 2021
                : 187
                : 2
                : 485-503
                Affiliations
                [1 ] Molecular Physiology, Heinrich-Heine-University Düsseldorf , Düsseldorf 40225, Germany
                [2 ] Institute of Transformative Bio-Molecules (WPI-ITbM), Nagoya University , Chikusa, Nagoya 464-8601, Japan
                [3 ] Cluster of Excellence on Plant Sciences, Heinrich-Heine-University Düsseldorf , Düsseldorf 40225, Germany
                [4 ] Institute for Cell and Interaction Biology, Heinrich-Heine-University Düsseldorf , Düsseldorf 40225, Germany
                [5 ] Agricultural Biotechnology Research Center, Academia Sinica , Taipei 115, Taiwan
                Author notes
                Author for communication: zcybele3@ 123456sinica.edu.tw
                [†]

                Senior authors.

                Author information
                https://orcid.org/0000-0003-0217-6731
                https://orcid.org/0000-0003-2568-7323
                https://orcid.org/0000-0002-4332-369X
                https://orcid.org/0000-0002-7107-4942
                https://orcid.org/0000-0001-7529-9244
                https://orcid.org/0000-0001-6465-0115
                https://orcid.org/0000-0002-0895-1914
                Article
                kiab353
                10.1093/plphys/kiab353
                8491070
                35237822
                68ec6af7-7b53-439a-8fc6-a242891c84a9
                © The Author(s) 2021. Published by Oxford University Press on behalf of American Society of Plant Biologists.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 9 June 2021
                : 12 July 2021
                Page count
                Pages: 19
                Funding
                Funded by: Deutsche Forschungsgemeinschaft (DFG, German Research Foundation;
                Funded by: Germany’s Excellence Strategy—EXC-2048/1—Project ID;
                Award ID: 390686111
                Funded by: SFB;
                Award ID: 1208—Project-ID 267205415
                Funded by: Alexander von Humboldt Professorship;
                Funded by: European Research Council (ERC) under the European Union’s Horizon 2020 research and innovation program;
                Award ID: 951292
                Funded by: Japan Society for the Promotion of Science (JSPS);
                Award ID: 19H000932
                Funded by: Heisenberg Professorship;
                Award ID: GR4559_4-1
                Funded by: DFG research grant;
                Award ID: GR4559_5-1
                Funded by: Human Frontier Science Program, DOI 10.13039/100004412;
                Funded by: Ministry of Science and Technology, DOI 10.13039/100007225;
                Award ID: MOST-109-2311-B-001-021
                Award ID: MOST-110-2923-B-001-002-MY3
                Funded by: Agricultural Biotechnology Research Center (ABRC) of Academia Sinica;
                Funded by: Japan Society for the Promotion of Science, DOI 10.13039/501100001691;
                Award ID: 20K21424
                Funded by: ITbM (World Premier International Research Center Initiative;
                Categories
                Focus Issue on Sensors and Controllers
                Update
                Biochemistry and Metabolism
                AcademicSubjects/SCI02286
                AcademicSubjects/SCI02287
                AcademicSubjects/SCI01270
                AcademicSubjects/SCI01280
                AcademicSubjects/SCI02288

                Plant science & Botany
                Plant science & Botany

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