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A novel red fluorescence dopamine biosensor selectively detects dopamine in the presence of norepinephrine in vitro

Dopamine (DA) and norepinephrine (NE) are pivotal neuromodulators that regulate a broad range of brain functions, often in concert. Despite their physiological importance, untangling the relationship between DA and NE in the fine control of output function is currently challenging, primarily due to...

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Autores principales: Nakamoto, Chihiro, Goto, Yuhei, Tomizawa, Yoko, Fukata, Yuko, Fukata, Masaki, Harpsøe, Kasper, Gloriam, David E., Aoki, Kazuhiro, Takeuchi, Tomonori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8647500/
https://www.ncbi.nlm.nih.gov/pubmed/34872607
http://dx.doi.org/10.1186/s13041-021-00882-8
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author Nakamoto, Chihiro
Goto, Yuhei
Tomizawa, Yoko
Fukata, Yuko
Fukata, Masaki
Harpsøe, Kasper
Gloriam, David E.
Aoki, Kazuhiro
Takeuchi, Tomonori
author_facet Nakamoto, Chihiro
Goto, Yuhei
Tomizawa, Yoko
Fukata, Yuko
Fukata, Masaki
Harpsøe, Kasper
Gloriam, David E.
Aoki, Kazuhiro
Takeuchi, Tomonori
author_sort Nakamoto, Chihiro
collection PubMed
description Dopamine (DA) and norepinephrine (NE) are pivotal neuromodulators that regulate a broad range of brain functions, often in concert. Despite their physiological importance, untangling the relationship between DA and NE in the fine control of output function is currently challenging, primarily due to a lack of techniques to allow the observation of spatiotemporal dynamics with sufficiently high selectivity. Although genetically encoded fluorescent biosensors have been developed to detect DA, their poor selectivity prevents distinguishing DA from NE. Here, we report the development of a red fluorescent genetically encoded GPCR (G protein-coupled receptor)-activation reporter for DA termed ‘R-GenGAR-DA’. More specifically, a circular permutated red fluorescent protein (cpmApple) was replaced by the third intracellular loop of human DA receptor D1 (DRD1) followed by the screening of mutants within the linkers between DRD1 and cpmApple. We developed two variants: R-GenGAR-DA1.1, which brightened following DA stimulation, and R-GenGAR-DA1.2, which dimmed. R-GenGAR-DA1.2 demonstrated a reasonable dynamic range (ΔF/F(0) = − 43%), DA affinity (EC(50) = 0.92 µM) and high selectivity for DA over NE (66-fold) in HeLa cells. Taking advantage of the high selectivity of R-GenGAR-DA1.2, we monitored DA in presence of NE using dual-color fluorescence live imaging, combined with the green-NE biosensor GRAB(NE1m), which has high selectivity for NE over DA (> 350-fold) in HeLa cells and hippocampal neurons grown from primary culture. Thus, this is a first step toward the multiplex imaging of these neurotransmitters in, for example, freely moving animals, which will provide new opportunities to advance our understanding of the high spatiotemporal dynamics of DA and NE in normal and abnormal brain function. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13041-021-00882-8.
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spelling pubmed-86475002021-12-07 A novel red fluorescence dopamine biosensor selectively detects dopamine in the presence of norepinephrine in vitro Nakamoto, Chihiro Goto, Yuhei Tomizawa, Yoko Fukata, Yuko Fukata, Masaki Harpsøe, Kasper Gloriam, David E. Aoki, Kazuhiro Takeuchi, Tomonori Mol Brain Methodology Dopamine (DA) and norepinephrine (NE) are pivotal neuromodulators that regulate a broad range of brain functions, often in concert. Despite their physiological importance, untangling the relationship between DA and NE in the fine control of output function is currently challenging, primarily due to a lack of techniques to allow the observation of spatiotemporal dynamics with sufficiently high selectivity. Although genetically encoded fluorescent biosensors have been developed to detect DA, their poor selectivity prevents distinguishing DA from NE. Here, we report the development of a red fluorescent genetically encoded GPCR (G protein-coupled receptor)-activation reporter for DA termed ‘R-GenGAR-DA’. More specifically, a circular permutated red fluorescent protein (cpmApple) was replaced by the third intracellular loop of human DA receptor D1 (DRD1) followed by the screening of mutants within the linkers between DRD1 and cpmApple. We developed two variants: R-GenGAR-DA1.1, which brightened following DA stimulation, and R-GenGAR-DA1.2, which dimmed. R-GenGAR-DA1.2 demonstrated a reasonable dynamic range (ΔF/F(0) = − 43%), DA affinity (EC(50) = 0.92 µM) and high selectivity for DA over NE (66-fold) in HeLa cells. Taking advantage of the high selectivity of R-GenGAR-DA1.2, we monitored DA in presence of NE using dual-color fluorescence live imaging, combined with the green-NE biosensor GRAB(NE1m), which has high selectivity for NE over DA (> 350-fold) in HeLa cells and hippocampal neurons grown from primary culture. Thus, this is a first step toward the multiplex imaging of these neurotransmitters in, for example, freely moving animals, which will provide new opportunities to advance our understanding of the high spatiotemporal dynamics of DA and NE in normal and abnormal brain function. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13041-021-00882-8. BioMed Central 2021-12-06 /pmc/articles/PMC8647500/ /pubmed/34872607 http://dx.doi.org/10.1186/s13041-021-00882-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Methodology
Nakamoto, Chihiro
Goto, Yuhei
Tomizawa, Yoko
Fukata, Yuko
Fukata, Masaki
Harpsøe, Kasper
Gloriam, David E.
Aoki, Kazuhiro
Takeuchi, Tomonori
A novel red fluorescence dopamine biosensor selectively detects dopamine in the presence of norepinephrine in vitro
title A novel red fluorescence dopamine biosensor selectively detects dopamine in the presence of norepinephrine in vitro
title_full A novel red fluorescence dopamine biosensor selectively detects dopamine in the presence of norepinephrine in vitro
title_fullStr A novel red fluorescence dopamine biosensor selectively detects dopamine in the presence of norepinephrine in vitro
title_full_unstemmed A novel red fluorescence dopamine biosensor selectively detects dopamine in the presence of norepinephrine in vitro
title_short A novel red fluorescence dopamine biosensor selectively detects dopamine in the presence of norepinephrine in vitro
title_sort novel red fluorescence dopamine biosensor selectively detects dopamine in the presence of norepinephrine in vitro
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8647500/
https://www.ncbi.nlm.nih.gov/pubmed/34872607
http://dx.doi.org/10.1186/s13041-021-00882-8
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