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PXD053048

PXD053048 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitleA multi-tissue longitudinal proteomics study to evaluate the suitability of post-mortem samples for pathophysiological research
DescriptionRecent developments in liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS)-based proteomics have drastically increased analytical depth and sample throughput, establishing a robust tool for comprehensive system-wide analyses. Such analyses are instrumental in studying the pathophysiology of diseases. One crucial source of material for this is post-mortem individuals. However, there is a significant gap in our understanding of the multi-organ temporal impacts of body decomposition on the proteome. This deficiency compromises result validity due to challenges in controlling the post-mortem interval (PMI). To address this, we reanalyzed published data to compare the effect of the PMI on the proteome alterations to the disease effects. Additionally, we conducted a clinically relevant time-course experiment using isogenic mice and applied LC-MS/MS in data-independent acquisition (DIA) mode to systematically study the proteome alterations post-mortem. Our experiment uncovered dramatic organ-specific protein regulation post-mortem, with only certain aspects attributable to protein autolysis suggesting active post-mortem protein regulation. Notably, the liver and spleen exhibited substantial proteome changes within hours of PMI, while the heart showed comparatively modest changes even after 96 hours. Subcellular fractionation of the heart led to an unexpected surge in the number of proteins exhibiting abundance differences early in PMI. We conducted a compressive analysis of semi-tryptic peptides for the first time, revealing distinct consensus motifs for different organs, indicating organ-specific protease activity. In conclusion, when designing LC-MS/MS-based studies, meticulous consideration of sample collection is crucial as PMI effects may outweigh disease effects. It is preferred that both experimental and control samples are taken in the operation room, especially for studies including subcellular fractionation or trans-organ comparison. In single-organ studies, the planning should involve careful control of the PMI, preferably by sample matching.
HostingRepositoryPRIDE
AnnounceDate2025-01-23
AnnouncementXMLSubmission_2025-01-23_09:41:47.453.xml
DigitalObjectIdentifier
ReviewLevelPeer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportUnsupported dataset by repository
PrimarySubmitterChristian Beusch
SpeciesList scientific name: Mus musculus (Mouse); NCBI TaxID: 10090;
ModificationListacetylated residue; monohydroxylated residue; iodoacetamide derivatized residue
InstrumentQ Exactive
Dataset History
RevisionDatetimeStatusChangeLog Entry
02024-06-12 11:10:23ID requested
12024-12-17 14:45:19announced
22025-01-23 09:26:41announced2025-01-23: Updated project metadata.
32025-01-23 09:41:48announced2025-01-23: Updated project metadata.
Publication List
10.1038/s42003-025-07515-z;
39824970;
Beusch CM, Braesch-Andersen K, Felldin U, Sabatier P, Widgren A, Bergquist J, Grinnemo KH, Rodin S, A multi-tissue longitudinal proteomics study to evaluate the suitability of post-mortem samples for pathophysiological research. Commun Biol, 8(1):78(2025) [pubmed]
Keyword List
submitter keyword: post-mortem, DIA,proteomics, cadaver
Contact List
Sergey Rodin
contact affiliationCardio-Thoracic Translational Medicine (CTTM) Lab, Department of Surgical Sciences, Uppsala University, 752 37 Uppsala, Sweden
contact emailsergey.rodin@uu.se
lab head
Christian Beusch
contact affiliationEmory University
contact emailchristian.beusch@gmail.com
dataset submitter
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