Kemp: Difference between revisions
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How do cells transmit information, and how do internal and external environments control this transmission? Our lab is | How do cells transmit information, and how do internal and external environments control this transmission? Our lab is investigating the mechanisms by which oxidative extracellular environments (such as those found in inflammation) and intracellular oxidation (initiated by receptor ligation) influence the ability of cells to signal properly. We are characterizing the temporal control of proteins thiol modifications due to oxidation through a strong synergy between computational and experimental methods. We use computational modeling techniques to study how signaling networks may be regulated by changes in protein activities due to thiol modifications arising from intra- or extracellularly produced reactive oxygen species. Experimentally, we are developing novel high-throughput biochemical assays to detect and quantify the glutathionylation and oxidation of proteins. | ||
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We are located in the Wallace H. Coulter Department of Biomedical Engineering administered jointly between Georgia Tech and Emory University School of Medicine. The lab is physically located on the Georgia Tech campus in the Petit Institute for Bioengineering and Bioscience. | We are located in the Wallace H. Coulter Department of Biomedical Engineering administered jointly between Georgia Tech and Emory University School of Medicine. The lab is physically located on the Georgia Tech campus in the Petit Institute for Bioengineering and Bioscience. | ||
Revision as of 20:14, 23 March 2009
The Kemp Lab
Redox Systems Biology at Georgia Tech
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How do cells transmit information, and how do internal and external environments control this transmission? Our lab is investigating the mechanisms by which oxidative extracellular environments (such as those found in inflammation) and intracellular oxidation (initiated by receptor ligation) influence the ability of cells to signal properly. We are characterizing the temporal control of proteins thiol modifications due to oxidation through a strong synergy between computational and experimental methods. We use computational modeling techniques to study how signaling networks may be regulated by changes in protein activities due to thiol modifications arising from intra- or extracellularly produced reactive oxygen species. Experimentally, we are developing novel high-throughput biochemical assays to detect and quantify the glutathionylation and oxidation of proteins.
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