The plasma proteome is highly dynamic and variable, composed of proteins derived from surrounding tissues and cells. To investigate the complex processes that contribute to the plasma proteome homeostasis we developed a mass spectrometry based proteomics strategy to infer the origin of proteins detected in murine plasma. The strategy relies on the construction of a comprehensive protein tissue atlas from cells and highly vascularized organs using shotgun mass spectrometry. The protein tissue atlas was transformed to a spectral library for highly reproducible quantification of tissue specific proteins directly in plasma using SWATH-like data-independent mass spectrometry analysis. We show that the method can determine drastic changes of tissue specific protein profiles in blood plasma from mouse animal models with sepsis. The strategy can be extended to several other species advancing our understanding of the complex processes that contribute to the plasma proteome homeostasis.
[dataset license: CC0 1.0 Universal (CC0 1.0)]
Keywords: Mouse ; organs ; plasma ; DIA ; sepsis ; MassIVE.quant reviewed - Gold
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Johan Malmstrom, Department of Clinical Sciences, Lund Division of Infection Medicine Sweden, N/A |
Submitting User: | ccms |
Malmström E, Kilsgård O, Hauri S, Smeds E, Herwald H, Malmström L, Malmström J.
Large-scale inference of protein tissue origin in gram-positive sepsis plasma using quantitative targeted proteomics.
Nat Commun. Epub 2016 Jan 6.
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