Evidence map›Paper›PMID 41097905›Full record

ReviewProteomics2025

Proteomics Insights Into Lysosome Biogenesis and Maturation.

Katharina Hirn, Sofía Fajardo-Callejón, Dominic Winter

Abstract readReview
In one paragraph

Review in Proteomics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Katharina HirnDepartment Metabolism, Senescence and Autophagy, Research Center One Health Ruhr, Medical Faculty, University Alliance Ruhr, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.ORCID 0009-0003-3478-6603
Sofía Fajardo-CallejónDepartment Metabolism, Senescence and Autophagy, Research Center One Health Ruhr, Medical Faculty, University Alliance Ruhr, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.ORCID 0009-0009-1013-425X
Dominic WinterDepartment Metabolism, Senescence and Autophagy, Research Center One Health Ruhr, Medical Faculty, University Alliance Ruhr, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.ORCID 0000-0001-6788-6641

Funding

German Academic Exchange ServiceGerman Research Council (DFG) Heisenberg ProgramNCL-Foundation
6 · The paper itself

Abstract

Lysosomes constitute the main degradative organelle of most eukaryotic cells and are capable of breaking down a wide spectrum of biomolecules, including proteins, lipids, glycans, and DNA/RNA. They play crucial roles in the regulation of cellular homeostasis, acting as metabolic signaling centers for the correlation of nutrient availability and biosynthetic processes. The lysosome's importance is highlighted by several human diseases associated with its dysfunction, including both early- and late-onset conditions, dependent on the level of functional impairment. Lysosomal biogenesis presents a multi-step process consisting of various delivery routes for its individual constituents, enabling strict activity control of the currently known ∼60 lysosomal hydrolases to prevent cellular self-digestion and proper assembly of the lysosomal membrane. In this review, we recapitulate the contribution of mass spectrometry (MS)-based proteomics to the characterization of lysosomal biogenesis in the last two decades. The enrichment and proteomic analysis of lysosomes and lysosomal proteins played an invaluable role for the investigation of lysosomes, encompassing the control of lysosomal gene expression, the characterization of sorting/trafficking processes, and the assignment of lysosomal proteins. This has resulted so far in the definition of ∼350 proteins which have been identified to be located in/at lysosomes or are of crucial importance for their function.

Indexed as

LysosomesProteomeProteomicsAnimalsHumansMass SpectrometryOrganelle BiogenesisProteinslysosomal proteinsProteinsProteomebiogenesislysosomal proteinslysosomemass spectrometrymaturationprotein traffickingproteomicsvesicular transport

Identifiers

PMID41097905
PMCPMC12645810

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.