Fig. 1.
Fig. 1. Distribution of radioiron between internalized ferritin and hemoglobin (Hb) following inhibition of protein degradation. DEC on day 8 of phase II were pulse labeled for 30 minutes with 4 nmol/L59Fe-ferritin, then washed and chased with 400 nmol/L unlabeled ferritin. Inhibition of protein degradation was initiated 60 minutes before the 59Fe-ferritin pulse by 20 μg/mL leupeptin or 15 μmol/L chloroquine, and inhibitors were present throughout the experiment. Leupeptin, which has a short half-life at 37°C, was added every 12 hours. Equal amounts of protein from cell lysates were analyzed on SDS-PAGE under nonreducing conditions followed by phosphor imaging and scanning with the phosphor imager.59Fe-Hb was expressed as percentage of the label in Hb and ferritin. [59Fe-Hb/(59Fe-Hb +59Fe-ferritin)] × 100. Unlabeled Hb was used as a marker (not shown).

Distribution of radioiron between internalized ferritin and hemoglobin (Hb) following inhibition of protein degradation. DEC on day 8 of phase II were pulse labeled for 30 minutes with 4 nmol/L59Fe-ferritin, then washed and chased with 400 nmol/L unlabeled ferritin. Inhibition of protein degradation was initiated 60 minutes before the 59Fe-ferritin pulse by 20 μg/mL leupeptin or 15 μmol/L chloroquine, and inhibitors were present throughout the experiment. Leupeptin, which has a short half-life at 37°C, was added every 12 hours. Equal amounts of protein from cell lysates were analyzed on SDS-PAGE under nonreducing conditions followed by phosphor imaging and scanning with the phosphor imager.59Fe-Hb was expressed as percentage of the label in Hb and ferritin. [59Fe-Hb/(59Fe-Hb +59Fe-ferritin)] × 100. Unlabeled Hb was used as a marker (not shown).

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