Proteomics

Dataset Information

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Depleted Prefractionated Human Plasma for Data Independent Acquisition Spectral Library


ABSTRACT: We established a spectral library for data-independent analysis of human plasma samples, using a pooled plasma sample from Danish adults. The samples were prepared for proteome analysis using an in-house developed protocol consuming one microliter of plasma per sample, and the tryptic digest and subsequent C18 purification was performed in 96-well plates. The spectral library consists of plasma which was analyzed neat (i.e. non-treated), and top 14 depleted. The samples were subjected to high pH reversed-phase peptide fractionated using C18 tips (8 fraction) and a HPLC system (20 fraction). The resulting peptides were analyzed on a Q Exactive with a capflow reversed-phase C18 LC-MS/MS setup in data-dependent mode. The final spectral library contains 21788 precursors and 1000 proteins (both at FDR<0.01).

INSTRUMENT(S): Q Exactive

ORGANISM(S): Homo Sapiens (human)

TISSUE(S): Blood Plasma

SUBMITTER: Tue Bjerg Bennike  

LAB HEAD: Hanno Steen

PROVIDER: PXD008163 | Pride | 2018-04-20

REPOSITORIES: Pride

Dataset's files

Source:
Action DRS
03_neat01.raw Raw
03_neat02.raw Raw
03_neat03.raw Raw
03_neat04.raw Raw
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Publications

A Cost-Effective High-Throughput Plasma and Serum Proteomics Workflow Enables Mapping of the Molecular Impact of Total Pancreatectomy with Islet Autotransplantation.

Bennike Tue Bjerg TB   Bellin Melena D MD   Xuan Yue Y   Stensballe Allan A   Møller Frederik Trier FT   Beilman Gregory J GJ   Levy Ofer O   Cruz-Monserrate Zobeida Z   Andersen Vibeke V   Steen Judith J   Conwell Darwin L DL   Steen Hanno H  

Journal of proteome research 20180419 5


Blood is an ideal body fluid for the discovery or monitoring of diagnostic and prognostic protein biomarkers. However, discovering robust biomarkers requires the analysis of large numbers of samples to appropriately represent interindividual variability. To address this analytical challenge, we established a high-throughput and cost-effective proteomics workflow for accurate and comprehensive proteomics at an analytical depth applicable for clinical studies. For validation, we processed 1 μL eac  ...[more]

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