蛋白质组
蛋白质组学
鸟枪蛋白质组学
计算生物学
定量蛋白质组学
生物
生物信息学
血液蛋白质类
化学
生物化学
基因
作者
Philipp E. Geyer,Nils A. Kulak,Garwin Pichler,Lesca M. Holdt,Daniel Teupser,Matthias Mann
出处
期刊:Cell systems
[Elsevier]
日期:2016-03-01
卷期号:2 (3): 185-195
被引量:579
标识
DOI:10.1016/j.cels.2016.02.015
摘要
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.
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