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Using MitER for 3D analysis of mitochondrial morphology and ER contacts.
Kichuk, Therese; Dhamankar, Satyen; Malani, Saurabh; Hofstadter, William A; Wegner, Scott A; Cristea, Ileana M; Avalos, José L.
Afiliação
  • Kichuk T; Department of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
  • Dhamankar S; Department of Chemical and Biological Engineering, Princeton University, Princeton, NJ 08544, USA.
  • Malani S; Department of Chemical and Biological Engineering, Princeton University, Princeton, NJ 08544, USA.
  • Hofstadter WA; Department of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
  • Wegner SA; Department of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
  • Cristea IM; Department of Molecular Biology, Princeton University, Princeton, NJ 08544, USA.
  • Avalos JL; Department of Molecular Biology, Princeton University, Princeton, NJ 08544, USA; Department of Chemical and Biological Engineering, Princeton University, Princeton, NJ 08544, USA; The Andlinger Center for Energy and the Environment, Princeton University, Princeton, NJ 08544, USA; High Meadows Enviro
Cell Rep Methods ; 4(1): 100692, 2024 Jan 22.
Article em En | MEDLINE | ID: mdl-38232737
ABSTRACT
We have developed an open-source workflow that allows for quantitative single-cell analysis of organelle morphology, distribution, and inter-organelle contacts with an emphasis on the analysis of mitochondria and mitochondria-endoplasmic reticulum (mito-ER) contact sites. As the importance of inter-organelle contacts becomes more widely recognized, there is a concomitant increase in demand for tools to analyze subcellular architecture. Here, we describe a workflow we call MitER (pronounced "mightier"), which allows for automated calculation of organelle morphology, distribution, and inter-organelle contacts from 3D renderings by employing the animation software Blender. We then use MitER to quantify the variations in the mito-ER networks of Saccharomyces cerevisiae, revealing significantly more mito-ER contacts within respiring cells compared to fermenting cells. We then demonstrate how this workflow can be applied to mammalian systems and used to monitor mitochondrial dynamics and inter-organelle contact in time-lapse studies.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Retículo Endoplasmático / Mitocôndrias Limite: Animals Idioma: En Revista: Cell Rep Methods Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Retículo Endoplasmático / Mitocôndrias Limite: Animals Idioma: En Revista: Cell Rep Methods Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos
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