A streamlined platform for high-content functional proteomics of primary human specimens

被引:189
作者
Jessani, N
Niessen, S
Wei, BQQ
Nicolau, M
Humphrey, M
Ji, YR
Han, WS
Noh, DY
Yates, JR
Jeffrey, SS
Cravatt, BF
机构
[1] Scripps Res Inst, Skaggs Inst Chem Biol, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Dept Cell Biol, La Jolla, CA 92037 USA
[3] Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA
[4] Stanford Univ, Sch Med, Dept Surg, Stanford, CA 94305 USA
[5] Seoul Natl Univ, Coll Med, Inst Canc Res, Seoul 110744, South Korea
[6] Seoul Natl Univ, Coll Med, Dept Surg, Seoul 110744, South Korea
关键词
D O I
10.1038/NMETH778
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Achieving information content of satisfactory breadth and depth remains a formidable challenge for proteomics. This problem is particularly relevant to the study of primary human specimens, such as tumor biopsies, which are heterogeneous and of finite quantity. Here we present a functional proteomics strategy that unites the activity-based protein profiling and multidimensional protein identification technologies (ABPP-MudPIT) for the streamlined analysis of human samples. This convergent platform involves a rapid initial phase, in which enzyme activity signatures are generated for functional classification of samples, followed by in-depth analysis of representative members from each class. Using this two-tiered approach, we identified more than 50 enzyme activities in human breast tumors, nearly a third of which represent previously uncharacterized proteins. Comparison with cDNA microarrays revealed enzymes whose activity, but not mRNA expression, depicted tumor class, underscoring the power of ABPP-MudPIT for the discovery of new markers of human disease that may evade detection by other molecular profiling methods.
引用
收藏
页码:691 / 697
页数:7
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