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. 2020 Jul 14;295(35):12498–12511. doi: 10.1074/jbc.RA120.013692

Figure 5.

Figure 5.

Molecular interaction of PT with VC1 and sRAGE. A, MST measurements were carried out in 20 mm HEPES, pH 7.1, 100 mm NaCl, 0.05% Tween 20 and standard capillaries with a constant concentration of fluorescently labeled prothrombin (100 nm) mixed with varying amounts of unlabeled VC1-His-Strep (final concentrations from 10.2 nm to 333 μm) or sRAGE (from 8.1 nm to 264 μm). After 30 min incubation at 24 °C, the samples were loaded into Monolith NT.115 capillaries (NanoTemper Technologies) and measurements were performed using the Monolith NT.115 (NanoTemper Technologies) at 20% LED power and medium MST power. The values of the dissociation constant (Kd) derived from the curves for the PT-VC1 interaction (n = 5 independent measurements) and for the PT-sRAGE interaction (n = 4 independent measurements) are indicated in the inset. B, MST measurements with VC1 were performed as in A, but in the presence of increasing concentrations of CaCl2 or in the presence of fluorescently labeled PT des-Gla instead of PT (n = 3 independent measurements). N/A, not applicable. In A and B, the fraction bound is plotted against the log10 of VC1 or sRAGE molar concentrations. The error bars on individual data points represent the standard deviations among the repeats.