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High-resolution functional proteomics by active-site peptide profiling
Author(s) -
Eric Okerberg,
Jiangyue Wu,
Baohong Zhang,
Babak Samii,
Kelly Blackford,
David T. Winn,
Kevin Shreder,
Jonathan J. Burbaum,
Matthew P. Patricelli
Publication year - 2005
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.0501205102
Subject(s) - proteome , proteomics , computational biology , protein function , biology , genome , high resolution , quantitative proteomics , bioinformatics , biochemistry , gene , geology , remote sensing
Characterization and functional annotation of the large number of proteins predicted from genome sequencing projects poses a major scientific challenge. Whereas several proteomics techniques have been developed to quantify the abundance of proteins, these methods provide little information regarding protein function. Here, we present a gel-free platform that permits ultrasensitive, quantitative, and high-resolution analyses of protein activities in proteomes, including highly problematic samples such as undiluted plasma. We demonstrate the value of this platform for the discovery of both disease-related enzyme activities and specific inhibitors that target these proteins.

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