Structural analysis of asunaprevir resistance in HCV NS3/4A protease
Department of Biochemistry and Molecular Pharmacology
Biochemistry | Biochemistry, Biophysics, and Structural Biology | Chemistry | Molecular Biology | Pharmacology | Structural Biology
Asunaprevir (ASV), an isoquinoline-based competitive inhibitor targeting the hepatitis C virus (HCV) NS3/4A protease, is very potent in vivo. However, the potency is significantly compromised by the drug resistance mutations R155K and D168A. In this study three crystal structures of ASV and an analogue were determined to analyze the structural basis of drug resistance susceptibility. These structures revealed that ASV makes extensive contacts with Arg155 outside the substrate envelope. Arg155 in turn is stabilized by Asp168, and thus when either residue is mutated, the enzyme's interaction with ASV's P2* isoquinoline is disrupted. Adding a P1-P3 macrocycle to ASV enhances the inhibitor's resistance barrier, likely due to poising the inhibitor to its bound conformation. Macrocyclic inhibitors with P2* extension moieties avoiding interaction with the protease S2 residues including Arg155 must be chosen for future design of more robust protease inhibitors.
DOI of Published Version
ACS Chem Biol. 2014 Nov 21;9(11):2485-90. doi: 10.1021/cb5006118. Epub 2014 Sep 30. Link to article on publisher's site
ACS chemical biology
Soumana D, Ali A, Schiffer CA. (2014). Structural analysis of asunaprevir resistance in HCV NS3/4A protease. Biochemistry and Molecular Pharmacology Publications and Presentations. https://doi.org/10.1021/cb5006118. Retrieved from https://escholarship.umassmed.edu/bmp_pp/201