An immunoaffinity liquid chromatography-tandem mass spectrometry assay for the quantitation of matrix metalloproteinase 9 in mouse serum

被引:50
|
作者
Ocana, Mireia Fernandez [1 ]
Neubert, Hendrik [2 ]
机构
[1] Pfizer Ltd, Expt Biol Sci, Sandwich CT13 9NJ, Kent, England
[2] Pfizer Ltd, PDM Biotherapeut & Translat Res, Sandwich CT13 9NJ, Kent, England
关键词
MMP-9; Mass spectrometry; Stable isotope-labeled peptide; Protein quantitation; Magnetic beads; Immunoaffinity; MATRIX-METALLOPROTEINASE ACTIVITY; ABSOLUTE QUANTIFICATION; MULTIPLEXED ASSAYS; PROTEIN BIOMARKERS; PEPTIDE; VALIDATION; EXPRESSION; ENRICHMENT; PLASMA; CANCER;
D O I
10.1016/j.ab.2010.01.002
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
An immunoaffinity liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was developed for the quantitation of the zinc endopeptidase matrix metalloproteinase 9 (MMP-9) from mouse serum. Sample preparation for the assay included magnetic bead-based enrichment using an MMP-9 antibody and was performed in a 96-well plate format using a liquid-handling robotic platform. The surrogate peptide GSPLQGPFLTAR derived from MMP-9 by trypsin digestion was monitored using an on-line capillary flow trap-release chromatography setup incorporating a series of trap columns (Cl 8, strong cation exchange, and another C18) prior to nanoflow chromatography and nanospray ionization with selected reaction monitoring (SRM) detection. The assay was fit-for-purpose validated and found to be accurate (<15% interbatch relative error) and precise (<15% interbatch coefficient of variation) across a range from 0.03 to 7.3 nM mouse MMP-9. Finally, the method was employed to measure MMP-9 concentrations in 30 naive mouse serum samples, and results were compared with those obtained by an immunoassay. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:202 / 210
页数:9
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