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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.
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页码:1551 / 1555
页数:5
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