Fig. 3
- ID
- ZDB-FIG-221113-3
- Publication
- Van Dycke et al., 2021 - A Novel Class of Norovirus Inhibitors Targeting the Viral Protease with Potent Antiviral Activity In Vitro and In Vivo
- Other Figures
- All Figure Page
- Back to All Figure Page
Compound 4 and rupintrivir block the norovirus protease. (A) The FRET signal was lost upon co-transfection with the wild-type (WT) or a mutated protease (A105V, I109V, A105V/I109V). The signal remained upon co-transfection with the inactive (H30A) protease. (B) Western blot of HEK293T cells co-transfected with the GI, GII or GV WT or mutant proteases along with the FRET construct. Cleavage was observed in the WT and mutant proteases in all genogroups. EV: empty vector. (C) Dose–response curves of compound 4 and rupintrivir on the WT proteases. Mean values ±SEM are presented, Mann–Whitney test **** p < 0.0001, ns: not significant. |