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. 2002 Feb 12;86(4):652–657. doi: 10.1038/sj.bjc.6600138

Figure 2.

Figure 2

Effect of photochemical treatment on gelonin-induced inhibition of protein synthesis. For the ‘light before’ strategy the cells were first incubated with 20 μg ml−1 AlPcS2a for 18 h, then for another 4 h in AlPcS2a-free medium before exposure to light as indicated in the figure. After illumination 1 μg ml−1 gelonin (gel) was added, and the cells were incubated for 18 h. For the ‘light after’ strategy the cells were co-incubated with 20 μg ml−1 AlPcS2a and 1 μg ml−1 gelonin for 18 h before light exposure. The control cells were treated only with 1 μg ml−1 gelonin for 18 h and exposed to light, or only with 20 μg ml−1 AlPcS2a for 18 h, chased 4 h in AlPcS2a-free medium and exposed to light. [3H]leucine incorporation into proteins was measured the day after the light-treatment. Data presented are the mean relative to non-illuminated cells. Data points represent mean±s.e. of triplicates.