A lysosomal biogenesis map reveals the cargo spectrum of yeast vacuolar protein targeting pathways

Author:

Eising Sebastian1ORCID,Esch Bianca1ORCID,Wälte Mike2,Vargas Duarte Prado3,Walter Stefan4,Ungermann Christian34ORCID,Bohnert Maria25ORCID,Fröhlich Florian13ORCID

Affiliation:

1. Molecular Membrane Biology Group, Department of Biology/Chemistry, Osnabrück University, Osnabrück, Germany

2. Institute of Cell Dynamics and Imaging, University of Münster, Münster, Germany

3. Biochemistry Section, Department of Biology/Chemistry, Osnabrück University, Osnabrück, Germany

4. Center of Cellular Nanoanalytics Osnabrück, Osnabrück University, Osnabrück, Germany

5. Cells in Motion Interfaculty Centre, University of Münster, Münster, Germany

Abstract

The lysosome is the major catabolic organelle in the cell that has been established as a key metabolic signaling center. Mutations in many lysosomal proteins have catastrophic effects and cause neurodegeneration, cancer, and age-related diseases. The vacuole is the lysosomal analog of Saccharomyces cerevisiae that harbors many evolutionary conserved proteins. Proteins reach vacuoles via the Vps10-dependent endosomal vacuolar protein sorting pathway, via the alkaline phosphatase (ALP or AP-3) pathway, and via the cytosol-to-vacuole transport (CVT) pathway. A systematic understanding of the cargo spectrum of each pathway is completely lacking. Here, we use quantitative proteomics of purified vacuoles to generate the yeast lysosomal biogenesis map. This dataset harbors information on the cargo–receptor relationship of almost all vacuolar proteins. We map binding motifs of Vps10 and the AP-3 complex and identify a novel cargo of the CVT pathway under nutrient-rich conditions. Our data show how organelle purification and quantitative proteomics can uncover fundamental insights into organelle biogenesis.

Funder

University of Münster

German Research Society

Publisher

Rockefeller University Press

Subject

Cell Biology

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