MRM-based multiplexed quantitation of 67 putative cardiovascular disease biomarkers in human plasma

被引:164
作者
Domanski, Dominik [2 ]
Percy, Andrew J. [2 ]
Yang, Juncong [2 ]
Chambers, Andrew G. [2 ]
Hill, John S. [3 ,4 ,5 ]
Freue, Gabriela V. Cohen [3 ]
Borchers, Christoph H. [1 ,2 ]
机构
[1] Univ Victoria, Dept Biochem & Microbiol, Genome BC Prote Ctr, Victoria, BC V8Z 7X8, Canada
[2] Univ Victoria, Genome British Columbia Prote Ctr, Victoria, BC V8Z 7X8, Canada
[3] PROOF Ctr Excellence, Vancouver, BC, Canada
[4] Univ British Columbia, St Pauls Hosp, James Hogg Res Ctr, Vancouver, BC V5Z 1M9, Canada
[5] Inst Heart Lung Hlth, Vancouver, BC, Canada
关键词
Biomarker; Biomedicine; Cardiovascular disease; MRM; Plasma; Quantitation; MONITORING MASS-SPECTROMETRY; C-REACTIVE PROTEIN; ABUNDANCE PROTEINS; LC/MS/MS METHOD; SERUM PROTEOME; QUANTIFICATION; ASSAYS; IDENTIFICATION; EFFICIENCY; DEPLETION;
D O I
10.1002/pmic.201100568
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A highly-multiplexed MRM-based assay for determination of cardiovascular disease (CVD) status and disease classification has been developed for clinical research. A high-flow system using ultra-high performance LC and an Agilent 6490 triple quadrupole mass spectrometer, equipped with an ion funnel, provided ease of use and increased the robustness of the assay. The assay uses 135 stable isotope-labeled peptide standards for the quantitation of 67 putative biomarkers of CVD in tryptic digests of whole plasma in a 30-min assay. Eighty-five analyses of the same sample showed no loss of sensitivity (<20% CV for 134/135 peptides) and no loss of retention time accuracy (<0.5% CV for all peptides). The maximum linear dynamic range of the MRM assays ranged from 103105 for 106 of the assays. Excellent linear responses (r >0.98) were obtained for 117 of the 135 peptide targets with attomole level limits of quantitation (<20% CV and accuracy 80120%) for 81 of the 135 peptides. The assay presented in this study is easy to use, robust, sensitive, and has high-throughput capabilities through short analysis time and complete automated sample preparation. It is therefore well suited for CVD biomarker validation and discovery in plasma.
引用
收藏
页码:1222 / 1243
页数:22
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