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Rapid subcellular calcium responses and dynamics by calcium sensor G-CatchER(+)
The precise spatiotemporal characteristics of subcellular calcium (Ca(2+)) transients are critical for the physiological processes. Here we report a green Ca(2+) sensor called “G-CatchER(+)” using a protein design to report rapid local ER Ca(2+) dynamics with significantly improved folding propertie...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7900224/ https://www.ncbi.nlm.nih.gov/pubmed/33665552 http://dx.doi.org/10.1016/j.isci.2021.102129 |
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author | Reddish, Florence N. Miller, Cassandra L. Deng, Xiaonan Dong, Bin Patel, Atit A. Ghane, Mohammad A. Mosca, Barbara McBean, Cheyenne Wu, Shengnan Solntsev, Kyril M. Zhuo, You Gadda, Giovanni Fang, Ning Cox, Daniel N. Mabb, Angela M. Treves, Susan Zorzato, Francesco Yang, Jenny J. |
author_facet | Reddish, Florence N. Miller, Cassandra L. Deng, Xiaonan Dong, Bin Patel, Atit A. Ghane, Mohammad A. Mosca, Barbara McBean, Cheyenne Wu, Shengnan Solntsev, Kyril M. Zhuo, You Gadda, Giovanni Fang, Ning Cox, Daniel N. Mabb, Angela M. Treves, Susan Zorzato, Francesco Yang, Jenny J. |
author_sort | Reddish, Florence N. |
collection | PubMed |
description | The precise spatiotemporal characteristics of subcellular calcium (Ca(2+)) transients are critical for the physiological processes. Here we report a green Ca(2+) sensor called “G-CatchER(+)” using a protein design to report rapid local ER Ca(2+) dynamics with significantly improved folding properties. G-CatchER(+) exhibits a superior Ca(2+) on rate to G-CEPIA1er and has a Ca(2+)-induced fluorescence lifetimes increase. G-CatchER(+) also reports agonist/antagonist triggered Ca(2+) dynamics in several cell types including primary neurons that are orchestrated by IP(3)Rs, RyRs, and SERCAs with an ability to differentiate expression. Upon localization to the lumen of the RyR channel (G-CatchER(+)-JP45), we report a rapid local Ca(2+) release that is likely due to calsequestrin. Transgenic expression of G-CatchER(+) in Drosophila muscle demonstrates its utility as an in vivo reporter of stimulus-evoked SR local Ca(2+) dynamics. G-CatchER(+) will be an invaluable tool to examine local ER/SR Ca(2+) dynamics and facilitate drug development associated with ER dysfunction. |
format | Online Article Text |
id | pubmed-7900224 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-79002242021-03-03 Rapid subcellular calcium responses and dynamics by calcium sensor G-CatchER(+) Reddish, Florence N. Miller, Cassandra L. Deng, Xiaonan Dong, Bin Patel, Atit A. Ghane, Mohammad A. Mosca, Barbara McBean, Cheyenne Wu, Shengnan Solntsev, Kyril M. Zhuo, You Gadda, Giovanni Fang, Ning Cox, Daniel N. Mabb, Angela M. Treves, Susan Zorzato, Francesco Yang, Jenny J. iScience Article The precise spatiotemporal characteristics of subcellular calcium (Ca(2+)) transients are critical for the physiological processes. Here we report a green Ca(2+) sensor called “G-CatchER(+)” using a protein design to report rapid local ER Ca(2+) dynamics with significantly improved folding properties. G-CatchER(+) exhibits a superior Ca(2+) on rate to G-CEPIA1er and has a Ca(2+)-induced fluorescence lifetimes increase. G-CatchER(+) also reports agonist/antagonist triggered Ca(2+) dynamics in several cell types including primary neurons that are orchestrated by IP(3)Rs, RyRs, and SERCAs with an ability to differentiate expression. Upon localization to the lumen of the RyR channel (G-CatchER(+)-JP45), we report a rapid local Ca(2+) release that is likely due to calsequestrin. Transgenic expression of G-CatchER(+) in Drosophila muscle demonstrates its utility as an in vivo reporter of stimulus-evoked SR local Ca(2+) dynamics. G-CatchER(+) will be an invaluable tool to examine local ER/SR Ca(2+) dynamics and facilitate drug development associated with ER dysfunction. Elsevier 2021-02-03 /pmc/articles/PMC7900224/ /pubmed/33665552 http://dx.doi.org/10.1016/j.isci.2021.102129 Text en © 2021 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Reddish, Florence N. Miller, Cassandra L. Deng, Xiaonan Dong, Bin Patel, Atit A. Ghane, Mohammad A. Mosca, Barbara McBean, Cheyenne Wu, Shengnan Solntsev, Kyril M. Zhuo, You Gadda, Giovanni Fang, Ning Cox, Daniel N. Mabb, Angela M. Treves, Susan Zorzato, Francesco Yang, Jenny J. Rapid subcellular calcium responses and dynamics by calcium sensor G-CatchER(+) |
title | Rapid subcellular calcium responses and dynamics by calcium sensor G-CatchER(+) |
title_full | Rapid subcellular calcium responses and dynamics by calcium sensor G-CatchER(+) |
title_fullStr | Rapid subcellular calcium responses and dynamics by calcium sensor G-CatchER(+) |
title_full_unstemmed | Rapid subcellular calcium responses and dynamics by calcium sensor G-CatchER(+) |
title_short | Rapid subcellular calcium responses and dynamics by calcium sensor G-CatchER(+) |
title_sort | rapid subcellular calcium responses and dynamics by calcium sensor g-catcher(+) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7900224/ https://www.ncbi.nlm.nih.gov/pubmed/33665552 http://dx.doi.org/10.1016/j.isci.2021.102129 |
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