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Originally published In Press as doi:10.1074/mcp.T100003-MCP200 on September 11, 2001.
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Molecular & Cellular Proteomics 1:60-68, 2002.
© 2002 by The American Society for Biochemistry and Molecular Biology, Inc.


Technology

Chemical Approaches for Functionally Probing the Proteome*

Doron Greenbaum{ddagger}, Amos Baruch§, Linda Hayrapetian§, Zsuzsanna Darula{ddagger}, Alma Burlingame{ddagger}, Katlin F. Medzihradszky{ddagger} and Matthew Bogyo§,||

{ddagger} Department of Pharmaceutical Chemistry, University of California, San Francisco, California 94143
§ Department of Biochemistry and Biophysics, University of California, San Francisco, California 94143
Mass Spectrometry Facility, Biological Research Center, Hungarian Academy of Sciences, H-6701 Szeged, Hungary

With the availability of complete genome sequences, emphasis has shifted toward the understanding of protein function. We have developed a functional proteomic methodology that makes use of chemically reactive fluorescent probes to profile and identify enzymes in complex mixtures by virtue of their catalytic activity. This methodology allows a comparison of changes in activity of multiple enzymes under a variety of conditions using a single two-dimensional separation. The probes can also be used to localize active enzymes in intact cells using fluorescence microscopy. Furthermore, the probes enable screens for selective small molecule inhibitors of each enzyme family member within crude lysates or intact cells. Ultimately, this technology allows the rapid identification of potential drug targets and small molecule lead compounds targeted to them.


|| To whom correspondence should be addressed: University of California, San Francisco Campus, Box 0448, 513 Parnassus Ave., San Francisco, CA 94143-0448. Tel.: 415-502-8142; Fax: 415-502-4315; E-mail: mbogyo{at}biochem.ucsf.edu.


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