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mCerulean3-Based Cameleon Sensor to Explore Mitochondrial Ca(2+) Dynamics In Vivo

Genetically Encoded Ca(2+) Indicators (GECIs) are extensively used to study organelle Ca(2+) homeostasis, although some available probes are still plagued by a number of problems, e.g., low fluorescence intensity, partial mistargeting, and pH sensitivity. Furthermore, in the most commonly used mitoc...

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Autores principales: Greotti, Elisa, Fortunati, Ilaria, Pendin, Diana, Ferrante, Camilla, Galla, Luisa, Zentilin, Lorena, Giacca, Mauro, Kaludercic, Nina, Di Sante, Moises, Mariotti, Letizia, Lia, Annamaria, Gómez-Gonzalo, Marta, Sessolo, Michele, Carmignoto, Giorgio, Bozio, Renato, Pozzan, Tullio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6581653/
https://www.ncbi.nlm.nih.gov/pubmed/31203189
http://dx.doi.org/10.1016/j.isci.2019.05.031
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author Greotti, Elisa
Fortunati, Ilaria
Pendin, Diana
Ferrante, Camilla
Galla, Luisa
Zentilin, Lorena
Giacca, Mauro
Kaludercic, Nina
Di Sante, Moises
Mariotti, Letizia
Lia, Annamaria
Gómez-Gonzalo, Marta
Sessolo, Michele
Carmignoto, Giorgio
Bozio, Renato
Pozzan, Tullio
author_facet Greotti, Elisa
Fortunati, Ilaria
Pendin, Diana
Ferrante, Camilla
Galla, Luisa
Zentilin, Lorena
Giacca, Mauro
Kaludercic, Nina
Di Sante, Moises
Mariotti, Letizia
Lia, Annamaria
Gómez-Gonzalo, Marta
Sessolo, Michele
Carmignoto, Giorgio
Bozio, Renato
Pozzan, Tullio
author_sort Greotti, Elisa
collection PubMed
description Genetically Encoded Ca(2+) Indicators (GECIs) are extensively used to study organelle Ca(2+) homeostasis, although some available probes are still plagued by a number of problems, e.g., low fluorescence intensity, partial mistargeting, and pH sensitivity. Furthermore, in the most commonly used mitochondrial Förster Resonance Energy Transfer based-GECIs, the donor protein ECFP is characterized by a double exponential lifetime that complicates the fluorescence lifetime analysis. We have modified the cytosolic and mitochondria-targeted Cameleon GECIs by (1) substituting the donor ECFP with mCerulean3, a brighter and more stable fluorescent protein with a single exponential lifetime; (2) extensively modifying the constructs to improve targeting efficiency and fluorescence changes caused by Ca(2+) binding; and (3) inserting the cDNAs into adeno-associated viral vectors for in vivo expression. The probes have been thoroughly characterized in situ by fluorescence microscopy and Fluorescence Lifetime Imaging Microscopy, and examples of their ex vivo and in vivo applications are described.
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spelling pubmed-65816532019-07-16 mCerulean3-Based Cameleon Sensor to Explore Mitochondrial Ca(2+) Dynamics In Vivo Greotti, Elisa Fortunati, Ilaria Pendin, Diana Ferrante, Camilla Galla, Luisa Zentilin, Lorena Giacca, Mauro Kaludercic, Nina Di Sante, Moises Mariotti, Letizia Lia, Annamaria Gómez-Gonzalo, Marta Sessolo, Michele Carmignoto, Giorgio Bozio, Renato Pozzan, Tullio iScience Article Genetically Encoded Ca(2+) Indicators (GECIs) are extensively used to study organelle Ca(2+) homeostasis, although some available probes are still plagued by a number of problems, e.g., low fluorescence intensity, partial mistargeting, and pH sensitivity. Furthermore, in the most commonly used mitochondrial Förster Resonance Energy Transfer based-GECIs, the donor protein ECFP is characterized by a double exponential lifetime that complicates the fluorescence lifetime analysis. We have modified the cytosolic and mitochondria-targeted Cameleon GECIs by (1) substituting the donor ECFP with mCerulean3, a brighter and more stable fluorescent protein with a single exponential lifetime; (2) extensively modifying the constructs to improve targeting efficiency and fluorescence changes caused by Ca(2+) binding; and (3) inserting the cDNAs into adeno-associated viral vectors for in vivo expression. The probes have been thoroughly characterized in situ by fluorescence microscopy and Fluorescence Lifetime Imaging Microscopy, and examples of their ex vivo and in vivo applications are described. Elsevier 2019-05-27 /pmc/articles/PMC6581653/ /pubmed/31203189 http://dx.doi.org/10.1016/j.isci.2019.05.031 Text en © 2019 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
Greotti, Elisa
Fortunati, Ilaria
Pendin, Diana
Ferrante, Camilla
Galla, Luisa
Zentilin, Lorena
Giacca, Mauro
Kaludercic, Nina
Di Sante, Moises
Mariotti, Letizia
Lia, Annamaria
Gómez-Gonzalo, Marta
Sessolo, Michele
Carmignoto, Giorgio
Bozio, Renato
Pozzan, Tullio
mCerulean3-Based Cameleon Sensor to Explore Mitochondrial Ca(2+) Dynamics In Vivo
title mCerulean3-Based Cameleon Sensor to Explore Mitochondrial Ca(2+) Dynamics In Vivo
title_full mCerulean3-Based Cameleon Sensor to Explore Mitochondrial Ca(2+) Dynamics In Vivo
title_fullStr mCerulean3-Based Cameleon Sensor to Explore Mitochondrial Ca(2+) Dynamics In Vivo
title_full_unstemmed mCerulean3-Based Cameleon Sensor to Explore Mitochondrial Ca(2+) Dynamics In Vivo
title_short mCerulean3-Based Cameleon Sensor to Explore Mitochondrial Ca(2+) Dynamics In Vivo
title_sort mcerulean3-based cameleon sensor to explore mitochondrial ca(2+) dynamics in vivo
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6581653/
https://www.ncbi.nlm.nih.gov/pubmed/31203189
http://dx.doi.org/10.1016/j.isci.2019.05.031
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