Proteolytic activity assayed by subcellular localization switching of a substrate |
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Authors: | Anne-Marie Szilvay Shirley Vanessa Sarria Monica Mannelqvist Rein Aasland Clemens Furnes |
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Affiliation: | 1. Department of Molecular Biology, University of Bergen, HIB, Post-box 7800, N-5020 Bergen, Norway;2. Centre for Organelle Research (CORE), University of Stavanger, Norway;3. Centre for Cancer Biomarkers CCBIO, Department of Clinical Medicine, University of Bergen, HIB, Post-box 7800, N-5020 Bergen, Norway |
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Abstract: | An approach to assay proteolytic activity in vivo by altering the subcellular localization of a labelled substrate was demonstrated. The assay included a protein shuttling between different cellular compartments and a site-specific recombinant protease. The shuttle protein used was the human immunodeficiency virus type 1 (HIV-1) Rev protein tandemly fused to the enhanced green fluorescent protein (EGFP) and the red fluorescent protein (RFP), while the protease was the site-specific protease VP24 from the herpes simplex virus type 1 (HSV-1). The fluorescent proteins in the Rev fusion protein were separated by a cleavage site specific for the VP24 protease. When co-expressed in COS-7 cells proteolysis was observed by fluorescence microscopy as a shift from a predominantly cytoplasmic localization of the fusion protein RevEGFP to a nuclear localization while the RFP part of the fusion protein remained in the cytoplasm. The cleavage of the fusion protein by VP24 was confirmed by Western blot analysis. The activity of VP24, when tagged N-terminally by the Myc-epitope, was found to be comparable to VP24. These results demonstrates that the activity and localization of a recombinantly expressed protease can be assessed by protease-mediated cleavage of fusion proteins containing a specific protease cleavage site. |
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Keywords: | Green fluorescent protein Red fluorescent protein HSV-1 protease HIV-1 Rev |
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