| Literature DB >> 29124938 |
Jian-Ying Zhou1, Lijun Chen1, Bai Zhang1, Yuan Tian1, Tao Liu2, Stefani N Thomas1, Li Chen1, Michael Schnaubelt1, Emily Boja3, Tara Hiltke3, Christopher R Kinsinger3, Henry Rodriguez3, Sherri R Davies4, Shunqiang Li4, Jacqueline E Snider4, Petra Erdmann-Gilmore4, David L Tabb5, R Reid Townsend4, Matthew J Ellis4, Karin D Rodland2, Richard D Smith2, Steven A Carr6, Zhen Zhang1, Daniel W Chan1, Hui Zhang1.
Abstract
Clinical proteomics requires large-scale analysis of human specimens to achieve statistical significance. We evaluated the long-term reproducibility of an iTRAQ (isobaric tags for relative and absolute quantification)-based quantitative proteomics strategy using one channel for reference across all samples in different iTRAQ sets. A total of 148 liquid chromatography tandem mass spectrometric (LC-MS/MS) analyses were completed, generating six 2D LC-MS/MS data sets for human-in-mouse breast cancer xenograft tissues representative of basal and luminal subtypes. Such large-scale studies require the implementation of robust metrics to assess the contributions of technical and biological variability in the qualitative and quantitative data. Accordingly, we derived a quantification confidence score based on the quality of each peptide-spectrum match to remove quantification outliers from each analysis. After combining confidence score filtering and statistical analysis, reproducible protein identification and quantitative results were achieved from LC-MS/MS data sets collected over a 7-month period. This study provides the first quality assessment on long-term stability and technical considerations for study design of a large-scale clinical proteomics project.Entities:
Keywords: Cancer Biology and Disease Human Proteome Project; clinical proteomics; iTRAQ; quantification; tumor tissues
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Year: 2017 PMID: 29124938 PMCID: PMC5850958 DOI: 10.1021/acs.jproteome.7b00362
Source DB: PubMed Journal: J Proteome Res ISSN: 1535-3893 Impact factor: 4.466