Proteomics

Dataset Information

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Localisation of Organelle Proteins using Data-Independent Acquisition (DIA-LOP)


ABSTRACT: Subcellular localisation within the proteome fundamentally influences cellular processes, however the development of high-throughput techniques to allow proteome-wide mapping of the cell has proven difficult. Here we present DIA-LOP, an approach capable of high-throughput spatial proteome mapping with in-depth subcellular resolution. This unified framework integrates differential-ultracentrifugation with ion-mobility-based data independent acquisition (DIA) mass spectrometry, alongside data processing using DIA-NN and spatial analysis within the pRoloc bioinformatics pipeline. Within the same experimental pipeline, we compare Differential-ultraCentrifugation (DC) fractionation with an alternate detergent-based protocol using both data-dependent (DDA) and data-independent acquisition (DIA) mass spectrometry approaches highlighting the increased subcellular resolution of the DC approach and the increased proteome coverage when DIA is applied. This study thus informs potential users of subcellular proteomics strategies that employ biochemical fractionation of the optimal workflows to achieve high proteome coverage and subcellular resolution.

INSTRUMENT(S):

ORGANISM(S): Homo Sapiens (human)

TISSUE(S): Cell Culture

SUBMITTER: Kieran McCaskie  

LAB HEAD: Kathryn S. Lilley

PROVIDER: PXD063082 | Pride | 2025-09-29

REPOSITORIES: Pride

Dataset's files

Source:
Action DRS
220813_SwissProt_Reviewed_Human_Proteome_NoIsoforms_Charl.fasta Fasta
220813_Universal_Protein_Contaminants_HaoGroup.fasta Fasta
3detergent_PSMs.txt Txt
3lopit_PSMs.txt Txt
D1_F1.raw Raw
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Publications

Localization of Organelle Proteins Using Data-Independent Acquisition (DIA-LOP).

McCaskie Kieran K   Hutchings Charlotte C   Feret Renata R   Kim Yong-In YI   Breckels Lisa L   Deery Michael M   Lilley Kathryn K  

Molecular & cellular proteomics : MCP 20250807 9


Subcellular localization within the proteome fundamentally influences cellular processes; however, the development of high-throughput techniques to allow proteome-wide mapping of the cell has proven difficult. Here we present DIA-LOP, an approach capable of high-throughput spatial proteome mapping with in-depth subcellular resolution. This unified framework integrates differential-ultracentrifugation (DC) with ion-mobility-based data-independent acquisition mass spectrometry, alongside data proc  ...[more]

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