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mCerulean3-Based Cameleon Sensor to Explore Mitochondrial Ca2+ 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; Di Lisa, Fabio; Carmignoto, Giorgio; Bozio, Renato; Pozzan, Tullio.
Afiliação
  • Greotti E; Neuroscience Institute, National Research Council (CNR), 35131 Padua, Italy; Department of Biomedical Sciences, University of Padua, 35131 Padua, Italy.
  • Fortunati I; Department of Chemical Sciences and INSTM, University of Padua, 35131 Padua, Italy.
  • Pendin D; Neuroscience Institute, National Research Council (CNR), 35131 Padua, Italy; Department of Biomedical Sciences, University of Padua, 35131 Padua, Italy.
  • Ferrante C; Department of Chemical Sciences and INSTM, University of Padua, 35131 Padua, Italy.
  • Galla L; Neuroscience Institute, National Research Council (CNR), 35131 Padua, Italy; Department of Biomedical Sciences, University of Padua, 35131 Padua, Italy.
  • Zentilin L; Molecular Medicine Laboratory, International Centre for Genetic Engineering and Biotechnology (ICGEB), 34149 Trieste, Italy.
  • Giacca M; Molecular Medicine Laboratory, International Centre for Genetic Engineering and Biotechnology (ICGEB), 34149 Trieste, Italy.
  • Kaludercic N; Neuroscience Institute, National Research Council (CNR), 35131 Padua, Italy; Department of Biomedical Sciences, University of Padua, 35131 Padua, Italy.
  • Di Sante M; Department of Biomedical Sciences, University of Padua, 35131 Padua, Italy.
  • Mariotti L; Neuroscience Institute, National Research Council (CNR), 35131 Padua, Italy; Department of Biomedical Sciences, University of Padua, 35131 Padua, Italy.
  • Lia A; Department of Biomedical Sciences, University of Padua, 35131 Padua, Italy.
  • Gómez-Gonzalo M; Neuroscience Institute, National Research Council (CNR), 35131 Padua, Italy; Department of Biomedical Sciences, University of Padua, 35131 Padua, Italy.
  • Sessolo M; Neuroscience Institute, National Research Council (CNR), 35131 Padua, Italy; Department of Biomedical Sciences, University of Padua, 35131 Padua, Italy.
  • Di Lisa F; Neuroscience Institute, National Research Council (CNR), 35131 Padua, Italy; Department of Biomedical Sciences, University of Padua, 35131 Padua, Italy.
  • Carmignoto G; Neuroscience Institute, National Research Council (CNR), 35131 Padua, Italy; Department of Biomedical Sciences, University of Padua, 35131 Padua, Italy.
  • Bozio R; Department of Chemical Sciences and INSTM, University of Padua, 35131 Padua, Italy.
  • Pozzan T; Neuroscience Institute, National Research Council (CNR), 35131 Padua, Italy; Department of Biomedical Sciences, University of Padua, 35131 Padua, Italy; Venetian Institute of Molecular Medicine (VIMM), 35131 Padua, Italy. Electronic address: tullio.pozzan@unipd.it.
iScience ; 16: 340-355, 2019 Jun 28.
Article em En | MEDLINE | ID: mdl-31203189
Genetically Encoded Ca2+ Indicators (GECIs) are extensively used to study organelle Ca2+ 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 Ca2+ 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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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: IScience Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: IScience Ano de publicação: 2019 Tipo de documento: Article