3CL protease from SARS-CoV-2 is a primary target for COVID-19 antiviral drug development. Here, we present a protocol for 3CL production in Escherichia coli. We describe steps to purify 3CL, expressed as a fusion with the Saccharomyces cerevisiae SUMO protein, with yields up to 120 mg L following cleavage. The protocol also provides isotope-enriched samples suitable for nuclear magnetic resonance (NMR) studies. We also present methods to characterize 3CL by mass spectrometry, X-ray crystallography, heteronuclear NMR, and a Förster-resonance-energy-transfer-based enzyme assay. For complete details on the use and execution of this protocol, please refer to Bafna et al..
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10160526 | PMC |
http://dx.doi.org/10.1016/j.xpro.2023.102326 | DOI Listing |
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