Table 3. Peptide-Based Inhibitors of HCV Entry, Their Sequences, and the Available Inhibition Data.
target | name | sequence | efficiency of inhibition |
---|---|---|---|
CD81 | 710–725178 | ASWAIKWEYVVLLFLL | ∼60% relative luciferase activity at 51 μMa |
CD81-binding nonapeptide182 | SPQYWTGA motif | NA | |
CL58179 | MANAGLQLLGFILAFLGW | IC50 = 2.1 ± 0.5 μM | |
E2 | hCD81-like nonapeptide184 | ATWVCGPCT | E2 inhibits binding of C9 clone to anti-hCD81 JS-81 with inhibition ratio of 67.5% |
SAHH-5181 | PSGSNXSNIISNXFRED | EC50 = 17–39 μMb | |
C18183 | WPWHNHR | Relative level of HCV RNA ∼ 0.5 at 97 μMc | |
E2–42180 | QGSWFGCTWMNSTGF | % of infectivity at C = 5 nM: 50–60% |
Luciferase activity in Huh7.5 cells compared to the activity in PBS buffer.
Value depending on the HCV subtype.
In Huh7.5 cells infected with HCVcc.