Fig. 1.
Fig. 1. Binding of PK to HUVEC. (A) The effect of HK and Zn+2 on biotin-PK binding to HUVECs. HUVECs were incubated with 20 nmol/L HK (□) for 1 hour at 37°C in the presence of 50 μmol/L Zn+2. Unbound HK was removed and biotin-PK (20 nmol/L) was added in HEPES-Tyrode's binding buffer containing Zn+2 for variable times. In other wells, HUVECs were incubated with biotin-PK (20 nmol/L) for variable times at 37°C in the absence of HK, but in the presence (⋄) or absence (○) of Zn+2. The specific binding of biotin-PK bound is shown. The data presented represent the mean ± SEM of three experiments. (B) Binding of 125I-PK (20 nmol/L) to HUVECs in suspension in HEPES-Tyrode's binding buffer containing 50 μmol/L Zn+2 in the absence (total binding; □) or presence (nonspecific binding; ⋄) of 50-fold molar excess PK. The points presented represent the mean ± SEM of three experiments. The absence of standard error bars at some points indicates that the variation was too low to indicate visually.

Binding of PK to HUVEC. (A) The effect of HK and Zn+2 on biotin-PK binding to HUVECs. HUVECs were incubated with 20 nmol/L HK (□) for 1 hour at 37°C in the presence of 50 μmol/L Zn+2. Unbound HK was removed and biotin-PK (20 nmol/L) was added in HEPES-Tyrode's binding buffer containing Zn+2 for variable times. In other wells, HUVECs were incubated with biotin-PK (20 nmol/L) for variable times at 37°C in the absence of HK, but in the presence (⋄) or absence (○) of Zn+2. The specific binding of biotin-PK bound is shown. The data presented represent the mean ± SEM of three experiments. (B) Binding of 125I-PK (20 nmol/L) to HUVECs in suspension in HEPES-Tyrode's binding buffer containing 50 μmol/L Zn+2 in the absence (total binding; □) or presence (nonspecific binding; ⋄) of 50-fold molar excess PK. The points presented represent the mean ± SEM of three experiments. The absence of standard error bars at some points indicates that the variation was too low to indicate visually.

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