Analysis for TNF-α using solid-phase affinity capture with radiolabel and MALDI-MS detection

被引:26
作者
Hurst, GB [1 ]
Buchanan, MV
Foote, LJ
Kennel, SJ
机构
[1] Oak Ridge Natl Lab, Div Chem & Analyt Sci, Oak Ridge, TN 37831 USA
[2] Oak Ridge Natl Lab, Div Life Sci, Oak Ridge, TN 37831 USA
关键词
D O I
10.1021/ac9905423
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Screening of mutant mice for subtle phenotypes requires sensitive,high-throughput analyses of sentinel proteins in functional pathways, The cytokine TNF-alpha is upregulated during inflammatory reactions associated with auto-immune diseases. We have developed a method to monitor the concentration of TNF-alpha under physiological conditions, TNF-alpha is captured, purified, and concentrated using monoclonal antibody-coated microbeads. The capture is efficient (>80%) and can be used in the concentration range <100 pg/mL to >50 ng/mL, as determined by detection of I-125-labeled TNF-alpha. The bead capture of TNF-alpha can be combined with direct detection by MALDI-MS for sample concentrations of >10 ng/mL. TNF-alpha can be captured and detected from diluted mouse serum, with minimal interferences observed in the MALDI spectrum. This method-is adaptable to high-throughput sample handling with microfluidic devices and automated mass spectrometric analysis.
引用
收藏
页码:4727 / 4733
页数:7
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