SARS-CoV-2 3CLpro displays faster self-maturation in vitro than SARS-CoV 3CLpro due to faster C-terminal cleavage

The coronavirus (CoV) disease 2019 (COVID-19) caused by the severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) has become a worldwide pandemic. The 3C-like protease (3CL(pro)), which cleaves 11 sites including its own N- and C-termini on the viral polyproteins, is essential for SARS-CoV-2 replication. In this study, we constructed the full-length inactive 3CL(pro) with N- and C-terminal extensions as substrates for monitoring self-cleavage by wild-type 3CL(pro). We found that the rate-limiting C-terminal self-cleavage rate of SARS-CoV-2 3CL(pro) was 35-fold faster than that of SARS-CoV 3CL(pro) using the Trx/GST-tagged C145A 3CL(pro) substrates. Since self-cleavage of 3CL(pro) is the initial step for maturation of other viral proteins, our study suggests more facile SARS-CoV-2 replication than that of SARS-CoV.

Automated summary

The self-cleavage rate of SARS-CoV-2 3CL(pro) is 35 times faster than that of SARS-CoV, implying that SARS-CoV-2 replication is more efficient.