Fig. 8.
Binding of αEC and γC to the αM I and αX I domains.
(A) Different concentrations of 125I-labeled ligands αEC (●) and γC (▾) in TBS, 1 mM CaCl2, and 1 mM MgCl2 were added to wells coated with 10 μg/mL of the recombinant αM I domain and incubated for 3 hours at 37°C. After washing with TBS and 0.05% Tween 20, bound radioactivity was measured and the amounts of bound ligands were calculated, with correction for nonspecific binding to BSA-coated wells. (B) Different concentrations of recombinant αX I domain produced as a fusion protein with GST in TBS containing 1 mM MgCl2, 1 mM CaCl2, 0.05% Tween 20, and 5% glycerol were added to microtiter plates coated with 50 μg/mL αEC (●) and γC (▾) and postcoated with 3% BSA. After incubation for 3 hours at 22°C, anti-GST mAb (1:5000) was added to the wells for an additional 1.5 hours. Binding of the I domains was then detected with a secondary goat anti–mouse IgG conjugated to alkaline phosphatase, with subsequent development of the reaction with p-nitrophenyl phosphate.