| Literature DB >> 27135364 |
Philipp E Geyer1, Nils A Kulak2, Garwin Pichler2, Lesca M Holdt3, Daniel Teupser3, Matthias Mann4.
Abstract
Proteins in the circulatory system mirror an individual's physiology. In daily clinical practice, protein levels are generally determined using single-protein immunoassays. High-throughput, quantitative analysis using mass-spectrometry-based proteomics of blood, plasma, and serum would be advantageous but is challenging because of the high dynamic range of protein abundances. Here, we introduce a rapid and robust "plasma proteome profiling" pipeline. This single-run shotgun proteomic workflow does not require protein depletion and enables quantitative analysis of hundreds of plasma proteomes from 1 μl single finger pricks with 20 min gradients. The apolipoprotein family, inflammatory markers such as C-reactive protein, gender-related proteins, and >40 FDA-approved biomarkers are reproducibly quantified (CV <20% with label-free quantification). Furthermore, we functionally interpret a 1,000-protein, quantitative plasma proteome obtained by simple peptide pre-fractionation. Plasma proteome profiling delivers an informative portrait of a person's health state, and we envision its large-scale use in biomedicine.Entities:
Keywords: apolipoproteins; blood analysis; clinic; disease; human; mass spectrometry; plasma proteome profile
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Year: 2016 PMID: 27135364 DOI: 10.1016/j.cels.2016.02.015
Source DB: PubMed Journal: Cell Syst ISSN: 2405-4712 Impact factor: 10.304