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. 2017 Mar 30;7:45407. doi: 10.1038/srep45407

Figure 8. Inhibition of various mutants of TASK-2 by co-expressed DrVSP activation.

Figure 8

(A and B) Averages of current traces recorded from a HEK-293 cell co-expressing WT TASK-2 or various truncated or point mutated channels together with DrVSP. The potential was held at −75 mV and a pulse to 80 mV with a duration of 40 s was given to activate DrVSP. The graphs report averages with SEMs of 5–10 experiments. The intracellular solution contained 1 mM ATP and 1 mM Mg2+. (C) Summary of results of effects of DrVSP activation on currents mediated by WT or mutant TASK-2 channels. The columns report the time taken for currents to decrease by 50% (t0.5) after stepping the voltage from −75 mV to 80 mV. The results are means ± SEM of 3–10 experiments. In red mutants that gave t0.5 values significantly smaller than WT with P < 0.05. White columns identify mutants that appeared to be inhibited more slowly than WT TASK-2.