Quantitative Urinary Proteome Analysis for Biomarker Evaluation in Chronic Kidney Disease

被引:204
|
作者
Jantos-Siwy, Justyna [1 ]
Schiffer, Eric [1 ]
Brand, Korbinian [2 ]
Schumann, Gerhard [2 ]
Rossing, Kasper [3 ]
Delles, Christian [4 ]
Mischak, Harald [1 ]
Metzger, Jochen [1 ]
机构
[1] Mosaiques Diagnost & Therapeut AG, D-30625 Hannover, Germany
[2] Hannover Med Sch, Inst Klin Chem, D-30623 Hannover, Germany
[3] Steno Diabet Ctr, DK-2820 Gentofte, Denmark
[4] Univ Glasgow, BHF Glasgow Cardiovasc Res Ctr, Glasgow, Lanark, Scotland
关键词
Biomarker quantification; chronic kidney disease; capillary electrophoresis coupled with mass spectrometry; urinary proteome analysis; STEM-CELL TRANSPLANTATION; CAPILLARY-ELECTROPHORESIS; MASS-SPECTROMETRY; DIABETIC-NEPHROPATHY; CREATININE EXCRETION; DISCOVERY; PROTEINURIA; VALIDATION; PREDICT; SAMPLES;
D O I
10.1021/pr800401m
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A limitation of proteomic methods with respect to their clinical applicability is the lack of possibilities to directly deduce the amount of a protein or peptide from a particular mass spectrometry (MS) spectrum. For quantification of chronic kidney disease (CKD)-specific urinary polypeptides in capillary electrophoresis coupled with mass spectrometry (CE-MS), we compared signal intensity calibration methods based on either urinary creatinine or stable isotope labeled synthetic marker analogues (absolute quantification) with those based on ion counting using highly abundant collagen fragments as nonmarker references (relative quantification). Our results indicate that relative quantification of biomarker excretion based on ion counts in reference to endogenous "housekeeping" peptides is sufficient for the determination of urinary polypeptide levels. The calculation of absolute concentrations via exogenous stable isotope-labeled peptide standards is of no additional benefit.
引用
收藏
页码:268 / 281
页数:14
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