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The proteasome plays essential roles in nearly all biological processes in plant defense and development, yet simple methods for displaying proteasome activities in extracts and living tissues are not available to plant science. Here, we introduce an easy and robust method to simultaneously display the activities of all three catalytic proteasome subunits in plant extracts or living plant tissues. The method is based on a membrane-permeable, small-molecule fluorescent probe that irreversibly reacts with the catalytic site of the proteasome catalytic subunits in an activity-dependent manner. Activities can be quantified from fluorescent protein gels and used to study proteasome activities in vitro and in vivo. We demonstrate that proteasome catalytic subunits can be selectively inhibited by aldehyde-based inhibitors, including the notorious caspase-3 inhibitor DEVD. Furthermore, we show that the proteasome activity, but not its abundance, is significantly increased in Arabidopsis upon treatment with benzothiadiazole (BTH). This upregulation of proteasome activity depends on NPR1, and occurs mostly in the cytoplasm. The simplicity, robustness and versatility of this method will make this method widely applicable in plant science.

Original publication

DOI

10.1111/j.1365-313X.2009.04122.x

Type

Journal article

Journal

Plant J

Publication Date

01/04/2010

Volume

62

Pages

160 - 170

Keywords

Amino Acid Sequence, Arabidopsis, Boron Compounds, Catalytic Domain, Cytoplasm, Fluorescent Dyes, Molecular Sequence Data, Oligopeptides, Plant Proteins, Protease Inhibitors, Proteasome Endopeptidase Complex, Substrate Specificity, Thiadiazoles