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. 2020 Aug 26;6(35):eabb5938. doi: 10.1126/sciadv.abb5938

Fig. 4. Polymorphisms that protect HCV from NAbs also increase the need for SR-BI to mediate subsequent CD81 interactions.

Fig. 4

(A to C) Receptor blocking of the entry of indicated HCV recombinants using a dilution series of antibody against CD81 (A), LDLr (B), and SR-BI (C). (D) Receptor blocking of the entry of indicated recombinants pre- and postviral attachment. (E) Neutralization of the indicated H77 recombinants with a dilution series of sCD81-LEL. (F) IC50 values against sCD81-LEL for the indicated H77 recombinants plotted against SR-BI entry dependency calculated as outlined in (C) (Bmax). The data were analyzed as described in Fig. 1 to estimate maximum attainable effect, Bmax (C), or to calculate IC50 values (E). (G) R2 values from IC50 values for the indicated monoclonal NAbs against H77 recombinants from (A) to (F) plotted against their corresponding SR-BI entry dependency calculated as outlined in (C) (Bmax) (see fig. S4B for correlation plots). All error bars represent SD. *Receptor blocking or neutralization sensitivity of the HCV recombinant was statistically significantly different from H77-FL.