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      Novel Genetically Encoded Bright Positive Calcium Indicator NCaMP7 Based on the mNeonGreen Fluorescent Protein

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          Abstract

          Green fluorescent genetically encoded calcium indicators (GECIs) are the most popular tool for visualization of calcium dynamics in vivo. However, most of them are based on the EGFP protein and have similar molecular brightnesses. The NTnC indicator, which is composed of the mNeonGreen fluorescent protein with the insertion of troponin C, has higher brightness as compared to EGFP-based GECIs, but shows a limited inverted response with an ΔF/F of 1. By insertion of a calmodulin/M13-peptide pair into the mNeonGreen protein, we developed a green GECI called NCaMP7. In vitro, NCaMP7 showed positive response with an ΔF/F of 27 and high affinity (K d of 125 nM) to calcium ions. NCaMP7 demonstrated a 1.7-fold higher brightness and similar calcium-association/dissociation dynamics compared to the standard GCaMP6s GECI in vitro. According to fluorescence recovery after photobleaching (FRAP) experiments, the NCaMP7 design partially prevented interactions of NCaMP7 with the intracellular environment. The NCaMP7 crystal structure was obtained at 1.75 Å resolution to uncover the molecular basis of its calcium ions sensitivity. The NCaMP7 indicator retained a high and fast response when expressed in cultured HeLa and neuronal cells. Finally, we successfully utilized the NCaMP7 indicator for in vivo visualization of grating-evoked and place-dependent neuronal activity in the visual cortex and the hippocampus of mice using a two-photon microscope and an NVista miniscope, respectively.

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          Most cited references37

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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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            A bright monomeric green fluorescent protein derived from Branchiostoma lanceolatum

            Despite the existence of fluorescent proteins spanning the entire visual spectrum, the bulk of modern imaging experiments continue to rely on variants of the green fluorescent protein derived from Aequorea victoria. Meanwhile, a great deal of recent effort has been devoted to engineering and improving red fluorescent proteins, and relatively little attention has been given to green and yellow variants. Here we report a novel monomeric yellow-green fluorescent protein, mNeonGreen, which is derived from a tetrameric fluorescent protein from the cephalochordate Branchiostoma lanceolatum. This fluorescent protein is the brightest monomeric green or yellow fluorescent protein yet described, performs exceptionally well as a fusion tag for traditional imaging as well as stochastic single-molecule superresolution imaging, and is an excellent FRET acceptor for the newest generation of cyan fluorescent proteins.
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              High-performance calcium sensors for imaging activity in neuronal populations and microcompartments

              Calcium imaging with genetically encoded calcium indicators (GECIs) is routinely used to measure neural activity in intact nervous systems. GECIs are frequently used in one of two different modes: to track activity in large populations of neuronal cell bodies, or to follow dynamics in subcellular compartments such as axons, dendrites and individual synaptic compartments. Despite major advances, calcium imaging is still limited by the biophysical properties of existing GECIs, including affinity, signal-to-noise ratio, rise and decay kinetics and dynamic range. Using structure-guided mutagenesis and neuron-based screening, we optimized the green fluorescent protein-based GECI GCaMP6 for different modes of in vivo imaging. The resulting jGCaMP7 sensors provide improved detection of individual spikes (jGCaMP7s,f), imaging in neurites and neuropil (jGCaMP7b), and may allow tracking larger populations of neurons using two-photon (jGCaMP7s,f) or wide-field (jGCaMP7c) imaging.
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                Author and article information

                Journal
                Int J Mol Sci
                Int J Mol Sci
                ijms
                International Journal of Molecular Sciences
                MDPI
                1422-0067
                28 February 2020
                March 2020
                : 21
                : 5
                : 1644
                Affiliations
                [1 ]National Research Center “Kurchatov Institute”, Moscow 123182, Russia; subach_om@ 123456nrcki.ru (O.M.S.); witkax@ 123456mail.ru (V.V.P.); annadronova@ 123456mail.ru (A.M.G.); Ivashkina_OI@ 123456nrcki.ru (O.I.I.); nikolaeva_ay@ 123456nrcki.ru (A.Y.N.); igra-voina@ 123456yandex.ru (D.A.K.); annavlaskina@ 123456yandex.ru (A.V.V.); Lazarenko_VA@ 123456nrcki.ru (V.A.L.); taniarakitina@ 123456yahoo.com (T.V.R.)
                [2 ]Institute for Advanced Brain Studies, M.V. Lomonosov Moscow State University, Moscow 119991, Russia; vsotskov@ 123456list.ru (V.P.S.); k.anokhin@ 123456gmail.com (K.V.A.)
                [3 ]P.K. Anokhin Research Institute of Normal Physiology, Moscow 125315, Russia; n.barykina@ 123456nphys.ru
                [4 ]Bach Institute of Biochemistry, Research Center of Biotechnology of the Russian Academy of Sciences, Moscow 119071, Russia; boiko_konstantin@ 123456inbi.ras.ru
                [5 ]M.M. Shemyakin and Yu.A. Ovchinnikov Institute of Bioorganic Chemistry, RAS, Moscow 117997, Russia; olegpodgorny@ 123456inbox.ru
                [6 ]Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency, Moscow 119435, Russia; annavarizhuk@ 123456gmail.com (A.M.V.); pozmge@ 123456gmail.com (G.E.P.)
                [7 ]Center for Precision Genome Editing and Genetic Technologies for Biomedicine, Moscow 119435, Russia
                [8 ]Center for Precision Genome Editing and Genetic Technologies for Biomedicine, Pirogov Russian National Research Medical University, Moscow 117997, Russia
                [9 ]N.K. Koltzov Institute of Developmental Biology, RAS, Moscow 119334, Russia
                [10 ]Massachusetts Institute of Technology, Cambridge, MA 02139, USA; kiryl.piatkevich@ 123456gmail.com (K.D.P.); esb@ 123456media.mit.edu (E.S.B.)
                [11 ]School of Life Sciences, Westlake University, Hangzhou 310024, China
                Author notes
                [* ]Correspondence: subach_fv@ 123456nrcki.ru ; Tel.: +07-499-196 7100-3389
                Author information
                https://orcid.org/0000-0002-1729-5744
                https://orcid.org/0000-0001-5835-8388
                https://orcid.org/0000-0002-1540-7677
                https://orcid.org/0000-0001-8229-189X
                https://orcid.org/0000-0002-7777-9468
                https://orcid.org/0000-0003-2720-7821
                Article
                ijms-21-01644
                10.3390/ijms21051644
                7084697
                32121243
                d7faf367-106b-4a9a-b7e8-1ac4b2a05dc8
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 08 February 2020
                : 25 February 2020
                Categories
                Article

                Molecular biology
                genetically encoded calcium indicator (geci),protein engineering,calcium imaging,crystal structure,ncamp7,high brightness,fluorescent protein

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