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. 2020 Jul 20;117(31):18711–18718. doi: 10.1073/pnas.2005341117

Fig. 1.

Fig. 1.

Binding kinetics between KRM1 and CV-A10 particles in neutral and acidic conditions. (A and C) SPR binding profiles of KRM1 to mature CV-A10 virions at pH 7.4 (A) and pH 5.5 (C). The viral particles were immobilized on the chip surface, and KRM1 was applied as the analyte via serial dilutions. (B and D) Binding profiles of KRM1 to empty CV-A10 capsids at pH 7.4 (B) and pH 5.5 (D). KD values are shown as the mean ± SEM of three independent experiments.