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dc.contributor.authorWelsch C
dc.contributor.authorShimakami T
dc.contributor.authorHartmann C
dc.contributor.authorYang Y
dc.contributor.authorDomingues FS
dc.contributor.authorLengauer T
dc.contributor.authorZeuzem S
dc.contributor.authorLemon SM
dc.date.accessioned2018-10-30T09:14:55Z
dc.date.available2018-10-30T09:14:55Z
dc.date.issued2012
dc.identifier.issn0016-5085
dc.identifier.urihttp://dx.doi.org/10.1053/j.gastro.2011.11.035
dc.identifier.urihttp://hdl.handle.net/10863/6720
dc.description.abstractBACKGROUND & AIMS: It is a challenge to develop direct-acting antiviral agents that target the nonstructural protein 3/4A protease of hepatitis C virus because resistant variants develop. Ketoamide compounds, designed to mimic the natural protease substrate, have been developed as inhibitors. However, clinical trials have revealed rapid selection of resistant mutants, most of which are considered to be pre-existing variants. METHODS: We identified residues near the ketoamide-binding site in x-ray structures of the genotype 1a protease, co-crystallized with boceprevir or a telaprevir-like ligand, and then identified variants at these positions in 219 genotype-1 sequences from a public database. We used side-chain modeling to assess the potential effects of these variants on the interaction between ketoamide and the protease, and compared these results with the phenotypic effects on ketoamide resistance, RNA replication capacity, and infectious virus yields in a cell culture model of infection. RESULTS: Thirteen natural binding-site variants with potential for ketoamide resistance were identified at 10 residues in the protease, near the ketoamide binding site. Rotamer analysis of amino acid side-chain conformations indicated that 2 variants (R155K and D168G) could affect binding of telaprevir more than boceprevir. Measurements of antiviral susceptibility in cell-culture studies were consistent with this observation. Four variants (ie, Q41H, I132V, R155K, and D168G) caused low-to-moderate levels of ketoamide resistance; 3 of these were highly fit (Q41H, I132V, and R155K). CONCLUSIONS: Using a comprehensive sequence and structure-based analysis, we showed how natural variation in the hepatitis C virus protease nonstructural protein 3/4A sequences might affect susceptibility to first-generation direct-acting antiviral agents. These findings increase our understanding of the molecular basis of ketoamide resistance among naturally existing viral variants.en_US
dc.language.isoenen_US
dc.rights
dc.titlePeptidomimetic escape mechanisms arise via genetic diversity in the ligand-binding site of the hepatitis C virus NS3/4A serine proteaseen_US
dc.typeArticleen_US
dc.date.updated2018-10-30T08:41:19Z
dc.language.isiEN-GB
dc.journal.titleGastroenterology
dc.description.fulltextnoneen_US


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