Proteomics

Dataset Information

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Proteome profiling of enriched lysosomes obtained from four commercial isolation methodologies.


ABSTRACT: Lysosomes are membrane-bound cell organelles that can be found in all mammalian cells. They contain digestive enzymes and are involved in multiple processes, including degradation of worn-out cell parts, antigen presentation and induction of programmed cell death. Mass spectrometry studies of lysosomes have been hampered by low sensitivity, since analysis of whole cell proteomes significantly reduce the detection of their relatively low abundant proteins. To overcome this issue, we applied 4 different commercial methods for the enrichment of lysosomes: gradient-based, filter-based, magnetic-bead based and subcellular fractionation, and performed quantitative proteomics analysis on these samples.

INSTRUMENT(S):

ORGANISM(S): Homo Sapiens (human)

TISSUE(S): Monocyte

DISEASE(S): Acute Leukemia

SUBMITTER: Paula Díez  

LAB HEAD: Paula Díez

PROVIDER: PXD040003 | Pride | 2026-02-23

REPOSITORIES: Pride

Dataset's files

Source:
Action DRS
E20222002910a.raw Raw
E20222002911a.raw Raw
E20222002912a.raw Raw
E20222002913a.raw Raw
E20222002914a.raw Raw
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Publications


Lysosomes, essential organelles involved in diverse cellular processes, are increasingly recognized as central players in the pathogenesis of numerous diseases. Due to their low abundance in whole-cell extracts, enrichment strategies are required for downstream analyses such as proteomics. Despite the availability of various lysosome isolation methods, including density gradient-based separation, filter-based approaches, magnetic bead-based isolation, and subcellular fractionation, a systematic,  ...[more]

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