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. 2007 Jun 1;129(5):943–955. doi: 10.1016/j.cell.2007.03.046

Figure 1.

Figure 1

Retrotranslocation and Degradation of Δgpαf-BOF

After pΔgpαf mRNA was translated in vitro in the presence of [35S]Met, SRP, microsomes, and either ɛBOF-Lys-tRNALys (lanes 1–9) or Lys-tRNALys (lanes 10–12), the microsomes were pelleted and then added to solutions containing ATP and either reticulocyte lysate (cytosol, lanes 1–3), lysate lacking hemoglobin (cytosol-Hb, lanes 4–6 and 10–12), or no lysate (no cytosol, lanes 7–9). The average percentages of Δgpαf-BOF radioactivity (A) and BOF emission (B) remaining at 15 and 30 min (0 min = 100%) for each sample are shown. (n = 7; ±3%–7% for 35S, ±2%–6% for BOF.) , Δgpαf-BOF; ∗∗, pΔgpαf-BOF.