Rapid empirical discovery of optimal peptides for targeted proteomics

被引:0
|
作者
Stergachis, Andrew B. [1 ]
MacLean, Brendan [1 ]
Lee, Kristen [1 ]
Stamatoyannopoulos, John A. [1 ,2 ]
MacCoss, Michael J. [1 ]
机构
[1] Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA 98195 USA
[2] Univ Washington, Sch Med, Dept Med, Seattle, WA USA
基金
美国国家卫生研究院;
关键词
MASS-SPECTROMETRY; QUANTITATIVE PROTEOMICS; SHOTGUN PROTEOMICS; PROTEIN; ASSAYS; EXPRESSION; PREDICTION; DATABASE; GENE;
D O I
10.1038/NMETH.1770
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We report a method for high-throughput, cost-efficient empirical discovery of optimal proteotypic peptides and fragment ions for targeted proteomics applications using in vitro-synthesized proteins. We demonstrate the approach using human transcription factors, which are typically difficult, low-abundance targets and empirically derived proteotypic peptides for 98% of the target proteins. We show that targeted proteomic assays developed using our approach facilitate robust in vivo quantification of human transcription factors.
引用
收藏
页码:1041 / +
页数:6
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