bioRxiv · 10.1101/2025.10.20.683451
The yeast peroxisomal proteome at absolute quantitative scale
Abstract
Peroxisomes are dynamic organelles vital for lipid metabolism and redox homeostasis. In Saccharomyces cerevisiae, the expression of peroxisomal proteins is tightly regulated in response to metabolic conditions. Here, we provide the first absolute quantification of the yeast peroxisomal proteome under peroxisome-inducing (oleate) and fermentative (glucose) conditions using a label-free mass spectrometry approach. We determined protein copy numbers for [~]4,500 proteins, including 99 peroxisomal and peroxisome-associated proteins. Our data reveal that the peroxisomal proteome is [~]3-fold higher abundant in oleate-grown cells, constituting 2.8% of the total proteome (corresponding to 2.01 x 106 protein copies) compared to 0.8% (6.67 x 105 protein copies) in glucose, reflecting the necessity for peroxisomal functions such as fatty acid beta-oxidation. Enzymes of the beta-oxidation and glyoxylate cycle showed up to >500-fold higher abundance in oleate. In contrast, core components of the peroxisomal protein import machinery (e.g., Pex5, Pex14) exhibited only moderate changes ([~]2- to 8-fold). In addition to metabolic enzymes and components of the peroxisomal protein import pathways, we provide copy number data for proteins involved in cellular stress response, peroxisome proliferation, division and organization, peroxisome-associated membrane contact sites, and metabolite transporter. Taken together, our dataset offers a quantitative framework of peroxisomal remodeling under different metabolic conditions and highlights the organelles adaptive flexibility, providing a valuable resource for future studies on peroxisome biology.
Source connections
Explore related subjects
Keep this discovery
Explore connections, maps & timelines
Das, H., Oeljeklaus, S., Maier, R., Bender, J., Warscheid, B.. 2025-10-21. The yeast peroxisomal proteome at absolute quantitative scale. https://doi.org/10.1101/2025.10.20.683451
Cite the original work for its findings. Save a collection to share your selection of sources.