Protein analysis on a proteomic scale

Eric Phizicky (), Philippe I. H. Bastiaens (), Heng Zhu (), Michael Snyder () and Stanley Fields ()
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Eric Phizicky: University of Rochester School of Medicine
Philippe I. H. Bastiaens: European Molecular Biology Laboratory
Heng Zhu: Cellular, and Developmental Biology
Michael Snyder: Cellular, and Developmental Biology
Stanley Fields: Howard Hughes Medical Institute, University of Washington

Nature, 2003, vol. 422, issue 6928, 208-215

Abstract: Abstract The long-term challenge of proteomics is enormous: to define the identities, quantities, structures and functions of complete complements of proteins, and to characterize how these properties vary in different cellular contexts. One critical step in tackling this goal is the generation of sets of clones that express a representative of each protein of a proteome in a useful format, followed by the analysis of these sets on a genome-wide basis. Such studies enable genetic, biochemical and cell biological technologies to be applied on a systematic level, leading to the assignment of biochemical activities, the construction of protein arrays, the identification of interactions, and the localization of proteins within cellular compartments.

Date: 2003
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DOI: 10.1038/nature01512

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