Peroxisome Staining in Mammalian Cells Using Peroxisome-Specific Probes

Peroxisomes are ubiquitous organelles with essential roles in human health, and their dysfunction leads to a spectrum of genetic disorders. Visualization of peroxisomes is key to identifying peroxisome dysfunction; however, progress has been limited by the lack of peroxisome-specific probes. By developing PeroxiSPY, peroxisome-specific probes that mimic natural peroxisome metabolites, we enabled real-time detection, tracking, and quantification of peroxisome dynamics in live mammalian cells. Additionally, the applications of this technique to patient cells with peroxisome disorders reveal pathological phenotypes. Here, we provide a detailed protocol for the detection of peroxisomes in live mammalian cells, as well as the detection of peroxisomes post-staining in fixed cells. We demonstrate how to stain peroxisomes in live cells using peroxisome-specific probes, focusing on the preparation of cells, timing of the procedure, reproducibility, and troubleshooting. These probes enable rapid, specific, and non-toxic live-cell detection of peroxisomes, offering a unique, quantitative method for assessing peroxisome function and its dysfunction in peroxisome-related disorders.

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Publication Details

Journal
Journal of Visualized Experiments
Published
2025-12-19
DOI
https://doi.org/10.3791/69405
Primary Topic
Peroxisome Proliferator-Activated Receptors
Type
article
Field-Weighted Citation Impact
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article

Peroxisome Staining in Mammalian Cells Using Peroxisome-Specific Probes

Milena Schuhmacher, Einat Zalckvar, Daniel Kaganovich, Ruth E. Carmichael et al.
Journal of Visualized Experiments
Peroxisome Proliferator-Activated Receptors
article

Peroxisome Staining in Mammalian Cells Using Peroxisome-Specific Probes

Milena Schuhmacher, Einat Zalckvar, Daniel Kaganovich, Ruth E. Carmichael, Luc Reymond, Triana Amen, Tamar Cohen, Charlotte Howman, Mor Yarshansky Shlomy, Melanie S. van Aerle
article en

Abstract

Peroxisomes are ubiquitous organelles with essential roles in human health, and their dysfunction leads to a spectrum of genetic disorders. Visualization of peroxisomes is key to identifying peroxisome dysfunction; however, progress has been limited by the lack of peroxisome-specific probes. By developing PeroxiSPY, peroxisome-specific probes that mimic natural peroxisome metabolites, we enabled real-time detection, tracking, and quantification of peroxisome dynamics in live mammalian cells. Additionally, the applications of this technique to patient cells with peroxisome disorders reveal pathological phenotypes. Here, we provide a detailed protocol for the detection of peroxisomes in live mammalian cells, as well as the detection of peroxisomes post-staining in fixed cells. We demonstrate how to stain peroxisomes in live cells using peroxisome-specific probes, focusing on the preparation of cells, timing of the procedure, reproducibility, and troubleshooting. These probes enable rapid, specific, and non-toxic live-cell detection of peroxisomes, offering a unique, quantitative method for assessing peroxisome function and its dysfunction in peroxisome-related disorders.

Journal of Visualized Experiments(226)
Bar-Ilan University (IL), University of Exeter (GB), Goodman (Japan) (JP), Health & Life (Taiwan) (TW), University of Southampton (GB), École Polytechnique Fédérale de Lausanne (CH)
Openalex Percentile: Top 62%
Peroxisome Proliferator-Activated Receptors
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Peroxisome Staining in Mammalian Cells Using Peroxisome-Specific Probes — Milena Schuhmacher, Einat Zalckvar, et al. · Journal of Visualized Experiments (2025) | TGRS Research Map | TGRS