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. 2010 Jan 29;285(14):10924–10938. doi: 10.1074/jbc.M109.083154

FIGURE 10.

FIGURE 10.

Specific [3H]5HT uptake (A), abolition of amphetamine-stimulated [3H]5HT release (B), and marked reduction in the affinity of [3H]imipramine (C), resulting from the truncation of the SERT N terminus. A, uptake of [3H]5HT was determined in HEK293 cells transiently expressing wild type SERT and Δ64SERT as outlined in the legend to Fig. 1. B, PCA-induced release was determined as in Fig. 2, and the concentration-response curves generated as in Fig. 3. C, saturation of [3H]imipramine binding was performed with membranes (20 μg) prepared from HEK293 cells transiently expressing wild type SERT and Δ64SERT as outlined in the legends to Figs. 7 and 8.