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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...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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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. |
format | Online Article Text |
id | pubmed-6581653 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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