High-Throughput Matrix-Assisted Laser Desorption Ionization-Time-of-Flight Mass Spectrometry Method for Quantification of Hepcidin in Human Urine

被引:29
|
作者
Anderson, Damon S. [1 ,3 ,4 ]
Heeney, Matthew M. [2 ,6 ]
Roth, Udo [5 ]
Menzel, Christoph [5 ]
Fleming, Mark D. [1 ,3 ]
Steen, Hanno [1 ,4 ]
机构
[1] Childrens Hosp, Dept Pathol, Boston, MA 02115 USA
[2] Childrens Hosp, Dept Med, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Pathol, Boston, MA 02115 USA
[4] Childrens Hosp, Prote Ctr, Boston, MA 02115 USA
[5] QIAGEN GmbH, D-40724 Hilden, Germany
[6] Harvard Univ, Sch Med, Dept Pediat, Boston, MA 02115 USA
关键词
INFLAMMATION; SERUM; HEMOCHROMATOSIS; MUTATIONS; REGULATOR; PEPTIDE; ANEMIA; IL-6;
D O I
10.1021/ac902479p
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Levels of the peptide hormone hepcidin negatively correlate with systemic iron status and are increased in disorders in which iron metabolism is secondarily dis-regulated, such as the anemia of chronic disease. Consequently, the ability to measure hepcidin in the clinical setting may have diagnostic value for a broad range of indications. We describe a novel quantitative matrix-assisted laser desorption ionization-time-of-flight (MALDI-TOF) mass spectrometry assay for hepcidin in human urine which involves (i) direct enrichment from minute volumes (5 mu L) of minimally treated urine on the surface of a functionalized chip, (ii) quantification by the use of a stable isotope labeled internal standard, and (iii) analysis by MALDI-TOF. Performance features include a wide linear range (1-1000 nM; LOQ 2.5 nM), high accuracy (90-110% recovery) and precision (intraday CV 12.11%; interday CV 13.21%), and a strong correlation upon interlaboratory cross validation with an existing immunoassay. The assay is simple, accurate, and efficient, and the high-throughput performance features of the assay make large-scale clinical research studies feasible.
引用
收藏
页码:1551 / 1555
页数:5
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