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      Optogenetic engineering to probe the molecular choreography of STIM1-mediated cell signaling

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          Abstract

          Genetically encoded photoswitches have enabled spatial and temporal control of cellular events to achieve tailored functions in living cells, but their applications to probe the structure-function relations of signaling proteins are still underexplored. We illustrate herein the incorporation of various blue light-responsive photoreceptors into modular domains of the stromal interaction molecule 1 (STIM1) to manipulate protein activity and faithfully recapitulate STIM1-mediated signaling events. Capitalizing on these optogenetic tools, we identify the molecular determinants required to mediate protein oligomerization, intramolecular conformational switch, and protein-target interactions. In parallel, we have applied these synthetic devices to enable light-inducible gating of calcium channels, conformational switch, dynamic protein-microtubule interactions and assembly of membrane contact sites in a reversible manner. Our optogenetic engineering approach can be broadly applied to aid the mechanistic dissection of cell signaling, as well as non-invasive interrogation of physiological processes with high precision.

          Abstract

          Optogenetic tools have been used to control cellular behaviours but their use to probe structure-function relations of signalling proteins are underexplored. Here the authors engineer optogenetic modules into STIM1 to dissect molecular details of STIM1-mediated signalling and control various cellular events.

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          Most cited references47

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          Store-Operated Calcium Channels.

          Store-operated calcium channels (SOCs) are a major pathway for calcium signaling in virtually all metozoan cells and serve a wide variety of functions ranging from gene expression, motility, and secretion to tissue and organ development and the immune response. SOCs are activated by the depletion of Ca(2+) from the endoplasmic reticulum (ER), triggered physiologically through stimulation of a diverse set of surface receptors. Over 15 years after the first characterization of SOCs through electrophysiology, the identification of the STIM proteins as ER Ca(2+) sensors and the Orai proteins as store-operated channels has enabled rapid progress in understanding the unique mechanism of store-operate calcium entry (SOCE). Depletion of Ca(2+) from the ER causes STIM to accumulate at ER-plasma membrane (PM) junctions where it traps and activates Orai channels diffusing in the closely apposed PM. Mutagenesis studies combined with recent structural insights about STIM and Orai proteins are now beginning to reveal the molecular underpinnings of these choreographic events. This review describes the major experimental advances underlying our current understanding of how ER Ca(2+) depletion is coupled to the activation of SOCs. Particular emphasis is placed on the molecular mechanisms of STIM and Orai activation, Orai channel properties, modulation of STIM and Orai function, pharmacological inhibitors of SOCE, and the functions of STIM and Orai in physiology and disease.
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            Protein modules and signalling networks.

            T. Pawson (1995)
            Communication between cells assumes particular importance in multicellular organisms. The growth, migration and differentiation of cells in the embryo, and their organization into specific tissues, depend on signals transmitted from one cell to another. In the adult, cell signalling orchestrates normal cellular behaviour and responses to wounding and infection. The consequences of breakdowns in this signalling underlie cancer, diabetes and disorders of the immune and cardiovascular systems. Conserved protein domains that act as key regulatory participants in many of these different signalling pathways are highlighted.
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              STIM proteins: dynamic calcium signal transducers.

              Stromal interaction molecule (STIM) proteins function in cells as dynamic coordinators of cellular calcium (Ca(2+)) signals. Spanning the endoplasmic reticulum (ER) membrane, they sense tiny changes in the levels of Ca(2+) stored within the ER lumen. As ER Ca(2+) is released to generate primary Ca(2+) signals, STIM proteins undergo an intricate activation reaction and rapidly translocate into junctions formed between the ER and the plasma membrane. There, STIM proteins tether and activate the highly Ca(2+)-selective Orai channels to mediate finely controlled Ca(2+) signals and to homeostatically balance cellular Ca(2+). Details are emerging on the remarkable organization within these STIM-induced junctional microdomains and the identification of new regulators and alternative target proteins for STIM.
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                Author and article information

                Contributors
                Hanwd@zju.edu.cn
                yun.huang@tamu.edu
                yubinzhou@tamu.edu
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                25 February 2020
                25 February 2020
                2020
                : 11
                : 1039
                Affiliations
                [1 ]ISNI 0000 0004 4687 2082, GRID grid.264756.4, Center for Translational Cancer Research, Institute of Biosciences and Technology, , Texas A&M University, ; Houston, TX 77030 USA
                [2 ]ISNI 0000 0004 1758 2270, GRID grid.412632.0, Department of Gastroenterology, , Key Laboratory of Hubei Province for Digestive System Disease, Renmin Hospital of Wuhan University, ; Wuhan, 430060 China
                [3 ]ISNI 0000 0004 1759 700X, GRID grid.13402.34, Department of Medical Oncology, Laboratory of Cancer Biology, Institute of Clinical Science, Sir Run Run Shaw Hospital, College of Medicine, , Zhejiang University, ; Hangzhou, Zhejiang China
                [4 ]ISNI 0000 0001 2360 039X, GRID grid.12981.33, Department of Oral and Maxillofacial Surgery, Sun Yat-sen Memorial Hospital, , Sun Yat-sen University, ; Guangzhou, Guangdong 510120 China
                [5 ]ISNI 0000 0004 4687 2082, GRID grid.264756.4, Center for Epigenetics and Disease Prevention, Institute of Biosciences and Technology, , Texas A&M University, ; Houston, TX 77030 USA
                [6 ]ISNI 0000 0004 4687 2082, GRID grid.264756.4, Department of Translational Medical Sciences, College of Medicine, , Texas A&M University, ; Houston, TX 77030 USA
                Author information
                http://orcid.org/0000-0001-5460-3446
                http://orcid.org/0000-0001-5950-9168
                Article
                14841
                10.1038/s41467-020-14841-9
                7042325
                32098964
                78bd4bc0-c97d-47c3-a60c-992f849745ae
                © The Author(s) 2020

                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
                : 4 July 2019
                : 6 February 2020
                Funding
                Funded by: the Welch Foundation: BE-1913-20190330; the American Cancer Society:RSG-16-215-01-TBE: the Cancer Prevention and Research Institute of Texas:RP170660
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                © The Author(s) 2020

                Uncategorized
                synthetic biology,calcium signalling
                Uncategorized
                synthetic biology, calcium signalling

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