The dynamic range problem in the analysis of the plasma proteome

被引:111
作者
Hortin, Glen L. [1 ]
Sviridov, Denis [1 ]
机构
[1] NIH, Dept Lab Med, Warren Magnuson Clin Ctr, Bethesda, MD 20892 USA
关键词
Plasma proteins; Plasma proteomics; Proteomics; Protein abundance; PROSTATE-SPECIFIC ANTIGEN; C-REACTIVE PROTEIN; HUMAN CHORIONIC-GONADOTROPIN; SERUM; VALUES; LEVEL; TSH;
D O I
10.1016/j.jprot.2009.07.001
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
One of the greatest challenges in analyzing the plasma proteome is the wide range of concentration of different proteins. The current study examines the range of protein concentration for 18 proteins measured over a year in a clinical laboratory to provide data on pathological extremes in protein concentrations. The complete measured range, from upper limits for albumin to lowest values for thyroid-stimulating hormone (TSH), represented more than 10 logs of molar abundance. A number of plasma proteins measured in the clinical laboratory varied over a concentration range spanning more than 4 logs, and limits of detection of clinical assays were inadequate to assess full concentration ranges of several proteins. Considering reported values from studies using higher sensitivity assays suggest that plasma concentrations of prostate-specific antigen (PSA), human chorionic gonadotropin (hCG), and cardiac troponin I vary by more than 7 logs. All of the plasma proteins measured in the present study represent secretory proteins or highly expressed components of specific tissues. Thus, the dynamic range for these components is likely to greatly underestimate the total range of protein concentration in the plasma proteome. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:629 / 636
页数:8
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