Quantitative proteome analysis of breast cancer cell lines using 18O-labeling and an accurate mass and time tag strategy

被引:33
作者
Patwardhan, Anil J.
Strittmatter, Eric F.
Camp, David G., II
Smith, Richard D.
Pallavicini, Maria G.
机构
[1] Univ Calif, Sch Nat Sci, Merced, CA 95344 USA
[2] Univ Calif San Francisco, Ctr Comprehens Canc, San Francisco, CA 94143 USA
[3] Pacific NW Natl Lab, Div Biol Sci, Richland, WA 99352 USA
[4] Pacific NW Natl Lab, Environm & Mol Sci Lab, Richland, WA 99352 USA
关键词
breast cancer; FT-ICR; MS; protein expression; quantitative analysis;
D O I
10.1002/pmic.200500582
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Proteome comparison of cell lines derived from cancer and normal breast epithelium provide opportunities to identify differentially expressed proteins and pathways associated with specific phenotypes. We employed O-16/O-18 peptide labeling, FT-ICR MS, and an accurate mass and time (AMT) tag strategy to simultaneously compare the relative abundance of hundreds of proteins in non-cancer and cancer cell lines derived from breast tissue. A cell line reference panel allowed relative protein abundance comparisons among multiple cell lines and across multiple experiments. A peptide database generated from multidimensional LC separations and MS/MS analysis was used for subsequent AMT tag-based peptide identifications. This peptide database represented a total of 2299 proteins, including 514 that were quantified in five cell lines using the AMT tag and O-16/O-11 strategies. Eighty-six proteins showed at least a threefold protein abundance change between cancer and non-cancer cell lines. Hierarchical clustering of protein abundance ratios revealed that several groups of proteins were differentially expressed between the cancer cell lines.
引用
收藏
页码:2903 / 2915
页数:13
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