Description
Here we present LipidCreator, a software that fully supports targeted lipidomics assay development. LipidCreator offers a comprehensive framework to compute MS/MS fragment masses for over 60 lipid classes. LipidCreator provides all functionalities needed to define fragments, manage stable isotope labeling, optimize collision energy and generate in silico spectral libraries. We validate LipidCreator assays computationally and analytically and prove that it is capable to generate large targeted experiments to analyze blood and to dissect lipid-signaling pathways such as in human platelets.
In MTBLS1381, to validate the performance and accuracy of the transition lists provided by LipidCreator and their applicabability on other MS platforms, we used the transition lists for targeted profiling of lipid mediators in human platelet material. Platelets were stimulated with 0.01 U/ml thrombin, 1 U/ml thrombin, 1 µg/ml CRP or 5 µg/ml CRP for 5 min. The MS profiling of unstimulated and stimulated platelet material (pellet and supernatant) was performed after HPLC separation on an AB Sciex QTrap 6500 (Applied Biosystems, Darmstadt, Germany) in negative mode. Samples were measured in triplicates, interspersed with blank and standard runs.
Studies linked to this manuscript include;
MTBLS1333; LipidCreator: Collision Energy Optimization and Fragment Intensity Prediction for Lipid Mediators - Thermo QExactive HF
MTBLS1334; LipidCreator: Collision Energy Optimization and Fragment Intensity Prediction for Lipid Mediators - Agilent QTof
MTBLS1369; LipidCreator: Platelet isolation and stimulation - Targeted Phospho- and Glycerolipid Profiling
MTBLS1375; LipidCreator: Targeted lipidomics analysis of Human Plasma samples and comparison with NIST SRM 1950 standard
MTBLS1376; LipidCreator: Targeted lipidomics analysis of S. cerevisiae to determine true and false identification
MTBLS1381; LipidCreator: Platelet isolation and stimulation - Targeted Lipid Mediator Profiling
MTBLS1382; LipidCreator: Platelet isolation and stimulation - DIA Lipid Mediator Validation
[dataset license:
CC0 1.0 Universal (CC0 1.0)]
Keywords: GNPS Metabolomics MetaboLights
Contact
Principal Investigators:
(in alphabetical order)
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Nils Hoffmann, Leibniz-Institut f�r Analytische Wissenschaften � ISAS � e.V., ISAS e.V.
Otto-Hahn-Stra�e 6b
44227 Dortmund, Germ
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caceves
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Originally identified proteins that were automatically
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SwissProt
human reference database.
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Number of distinct protein accessions reported across all analyses (original submission and
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Number of distinct peptide sequences (including modified variants or peptidoforms) reported
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Number of distinct proteins quantified across all analyses (original submission and reanalyses)
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Distinct protein accessions are counted across all files submitted in the "Statistical Analysis
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Number of distinct proteins found to be differentially abundant in at least one comparison
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A protein is differentially abundant if its change in abundance across conditions is found
to be statistically significant with an adjusted p-value <= 0.05 and lists no issues associated
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Distinct protein accessions are counted across all files submitted in the "Statistical Analysis
of Quantified Analytes" category having a "Protein" column in this dataset.
"N/A" means no results of this type were submitted.
This dataset may not contain all raw spectra data as originally deposited in PRIDE.
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