Table 2.
Effects of Cu-Phen on the amplitude and voltage dependence of WT KCNQ2 and S4 cysteine mutants
| Channel | V50 | V50-Cu-Phen | ICu-Phena |
| mV | mV | ||
| WT Q2 | −32.2 ± 1.4 (10) | −29.5 ± 1.1 (10) | 1.07 ± 0.11 (10) |
| S195C Q2 | 5.2 ± 4.0b (8) | 0.8 ± 6.0b (8) | 0.26 ± 0.06b (8) |
| R198C Q2 | −31.0 ± 4.4 (7) | −5.3 ± 4.8 (7) | 0.27 ± 0.06b (7) |
| R201C Q2 | — | — | 0.33 ± 0.07b (7) |
Xenopus oocytes were incubated for 2 min at −80 mV in ND96 solution in the absence or presence of 100 µM Cu-Phen, washed with ND96 for another 5 min at −80 mV, and then depolarized from −90 to 45 mV in 15-mV increments and repolarized at −60 mV. Conductance–voltage relations were constructed and data were fitted to a single Boltzmann function to yield the V50 values. The values in parentheses correspond to the number of cells examined. Data are expressed as mean ± SEM.
The change in current amplitude was expressed as a ratio ICu-Phen of the current measured in the same cell at 45 mV after and before Cu-Phen application at −80 mV.
Statistically different from the WT KCNQ2 value, calculated by two-tailed unpaired Student’s t test, assuming equal variances; P < 0.01.