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Fluorescent fatty acid conjugates for live cell imaging of peroxisomes

Author

Listed:
  • Daria Korotkova

    (Ecole Polytechnique Fédérale de Lausanne (EPFL))

  • Anya Borisyuk

    (Ecole Polytechnique Fédérale de Lausanne (EPFL))

  • Anthony Guihur

    (University of Lausanne)

  • Manon Bardyn

    (Ecole Polytechnique Fédérale de Lausanne (EPFL))

  • Fabien Kuttler

    (Ecole Polytechnique Fédérale de Lausanne (EPFL))

  • Luc Reymond

    (Ecole Polytechnique Fédérale de Lausanne (EPFL))

  • Milena Schuhmacher

    (Ecole Polytechnique Fédérale de Lausanne (EPFL))

  • Triana Amen

    (Ecole Polytechnique Fédérale de Lausanne (EPFL)
    University of Southampton)

Abstract

Peroxisomes are eukaryotic organelles that are essential for multiple metabolic pathways, including fatty acid oxidation, degradation of amino acids, and biosynthesis of ether lipids. Consequently, peroxisome dysfunction leads to pediatric-onset neurodegenerative conditions, including Peroxisome Biogenesis Disorders (PBD). Due to the dynamic, tissue-specific, and context-dependent nature of their biogenesis and function, live cell imaging of peroxisomes is essential for studying peroxisome regulation, as well as for the diagnosis of PBD-linked abnormalities. However, the peroxisomal imaging toolkit is lacking in many respects, with no reporters for substrate import, nor cell-permeable probes that could stain dysfunctional peroxisomes. Here we report that the BODIPY-C12 fluorescent fatty acid probe stains functional and dysfunctional peroxisomes in live mammalian cells. We then go on to improve BODIPY-C12, generating peroxisome-specific reagents, PeroxiSPY650 and PeroxiSPY555. These probes combine high peroxisome specificity, bright fluorescence in the red and far-red spectrum, and fast non-cytotoxic staining, making them ideal tools for live cell, whole organism, or tissue imaging of peroxisomes. Finally, we demonstrate that PeroxiSPY enables diagnosis of peroxisome abnormalities in the PBD CRISPR/Cas9 cell models and patient-derived cell lines.

Suggested Citation

  • Daria Korotkova & Anya Borisyuk & Anthony Guihur & Manon Bardyn & Fabien Kuttler & Luc Reymond & Milena Schuhmacher & Triana Amen, 2024. "Fluorescent fatty acid conjugates for live cell imaging of peroxisomes," Nature Communications, Nature, vol. 15(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-48679-2
    DOI: 10.1038/s41467-024-48679-2
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    References listed on IDEAS

    as
    1. Qixin Chen & Hongbao Fang & Xintian Shao & Zhiqi Tian & Shanshan Geng & Yuming Zhang & Huaxun Fan & Pan Xiang & Jie Zhang & Xiaohe Tian & Kai Zhang & Weijiang He & Zijian Guo & Jiajie Diao, 2020. "A dual-labeling probe to track functional mitochondria–lysosome interactions in live cells," Nature Communications, Nature, vol. 11(1), pages 1-10, December.
    2. Peiqiang Feng & Xudong Wu & Satchal K. Erramilli & Joao A. Paulo & Pawel Knejski & Steven P. Gygi & Anthony A. Kossiakoff & Tom A. Rapoport, 2022. "A peroxisomal ubiquitin ligase complex forms a retrotranslocation channel," Nature, Nature, vol. 607(7918), pages 374-380, July.
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