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. Author manuscript; available in PMC: 2011 Jul 12.
Published in final edited form as: Biochem J. 2010 Nov 25;432(3):585–594. doi: 10.1042/BJ20100878

Figure 3. Inhibition of Proteasome induction by cyclohexamide.

Figure 3

Panel A. MEF cells were incubated with 100 μg/ml of cyclohexamide (or not treated) in an attempt to block H2O2 induced expression of proteolytic enzymes. Cells were then grown to 50% confluence and exposed (in PBS) to a transient adaptive pre-treatment 2 μmol of H202 per 107 cells, harvested, and lysed, as described in the legend to Figure. 1. Proteolytic activity assays for degradation of suc-LLVY-AMC were then performed, as per Figs. 1 and 2. Panel B. Inhibition of proteasome induction plotted as the percent inhibition (means ± SE, n = 3) exerted by cycloheximide against the H2O2 induced (adaptive) proteasome activity of panel A.