3C-like proteinase from SARS coronavirus catalyzes substrate hydrolysis by a general base mechanism
SARS 3C-like proteinase has been proposed to be a key enzyme for drug design against
SARS. Lack of a suitable assay has been a major hindrance for enzyme kinetic studies and
a large-scale inhibitor screen for SARS 3CL proteinase. Since SARS 3CL proteinase
belongs to the cysteine protease family (family C3 in clan CB) with a chymotrypsin fold, it is
important to understand the catalytic mechanism of SARS 3CL proteinase to determine
whether the proteolysis proceeds through a general base catalysis mechanism like …
SARS. Lack of a suitable assay has been a major hindrance for enzyme kinetic studies and
a large-scale inhibitor screen for SARS 3CL proteinase. Since SARS 3CL proteinase
belongs to the cysteine protease family (family C3 in clan CB) with a chymotrypsin fold, it is
important to understand the catalytic mechanism of SARS 3CL proteinase to determine
whether the proteolysis proceeds through a general base catalysis mechanism like …
SARS 3C-like proteinase has been proposed to be a key enzyme for drug design against SARS. Lack of a suitable assay has been a major hindrance for enzyme kinetic studies and a large-scale inhibitor screen for SARS 3CL proteinase. Since SARS 3CL proteinase belongs to the cysteine protease family (family C3 in clan CB) with a chymotrypsin fold, it is important to understand the catalytic mechanism of SARS 3CL proteinase to determine whether the proteolysis proceeds through a general base catalysis mechanism like chymotrypsin or an ion pair mechanism like papain. We have established a continuous colorimetric assay for SARS 3CL proteinase and applied it to study the enzyme catalytic mechanism. The proposed catalytic residues His41 and Cys145 were confirmed to be critical for catalysis by mutating to Ala, while the Cys145 to Ser mutation resulted in an active enzyme with a 40-fold lower activity. From the pH dependency of catalytic activity, the pKa's for His41 and Cys145 in the wild-type enzyme were estimated to be 6.38 and 8.34, while the pKa's for His41 and Ser145 in the C145S mutant were estimated to be 6.15 and 9.09, respectively. The C145S mutant has a normal isotope effect in D2O for general base catalysis, that is, reacts slower in D2O, while the wild-type enzyme shows an inverse isotope effect which may come from the lower activation enthalpy. The pKa values measured for the active site residues and the activity of the C145S mutant are consistent with a general base catalysis mechanism and cannot be explained by a thiolate−imidazolium ion pair model.
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