Real-time evaluation of experimental variation in large-scale LC-MS/MS-based quantitative proteomics of complex samples

被引:19
|
作者
Levin, Yishai [1 ]
Wang, Lan [1 ]
Ingudomnukul, Erin [2 ]
Schwarz, Emanuel [1 ]
Baron-Cohen, Simon [2 ]
Palotas, Andras [3 ]
Bahn, Sabine [1 ]
机构
[1] Univ Cambridge, Inst Biotechnol, Cambridge CB2 1QT, England
[2] Univ Cambridge, Autism Res Ctr, Dept Psychiat, Cambridge CB2 8AH, England
[3] Asklepios Med Bt, Private Practice & Res Ctr, H-6722 Szeged, Hungary
基金
英国医学研究理事会;
关键词
Proteomics; LC-MS; MSE; NanoUPLC; Serum; Fibroblasts; QC; Biomarker discovery; MASS-SPECTROMETRY; BIOMARKER DISCOVERY; QUANTIFICATION;
D O I
10.1016/j.jchromb.2008.11.007
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Quantitative proteomic profiling is becoming a widely used approach in systems biology and biomarker discovery. There is a growing realization that quantitative studies require high numbers of unpooled samples for increased statistical power. Large-scale quantitative analyses require an added degree of stringency due to the lengthy study periods and reliance on stability of analytical instrumentation. We present the inclusion of quality control samples alongside clinical samples in the preparation and nanoLC-MS analysis pipelines. These serve the purpose of monitoring, evaluating and reporting experimental variation measured in real-time. This concept is shown for two types of complex biological samples: serum samples and fibroblast samples. In both studies QC samples were added among dozens of clinical ones and analyzed using a label-free quantitative proteomic platform. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:1299 / 1305
页数:7
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