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. 2017 Feb 20;7:41095. doi: 10.1038/srep41095

Table 1. Voltage-dependence of activation.

  V1/2 (mV) k (mV)
WT N −31.6 ± 1.7     16.0 ± 0.9    
WT E −34.5 ± 2.3   12.3 ± 1.4  
V404I N −9.5 ± 1.4 **** ]+++ 14.7 ± 1.1    
V404I E −20.3 ± 1.5 *** 14.2 ± 0.9  
I407M N −1.9 ± 0.8 ****   10.7 ± 0.2 *** ]++
I407M E 2.5 ± 1.1 **** 9.4 ± 0.2  
V408A N −29.4 ± 0.9     9.1 ± 1.0 ***  
V408A E −23.6 ± 3.4   8.1 ± 0.4  

Voltage-dependence of activation was determined by fitting data to a Boltzmann function, equation (2), to determine the midpoint of channel activation (V1/2) and relative voltage sensitivity (k). All data are represented as mean ± SEM, n = 4–8 oocytes for each channel type. Edited (E) and non-edited (N) isoforms of the mutant channels were compared to WT E and WT N channels, respectively: ***p ≤ 0.001; ****p < 0.0001. All types of N channels were compared to their respective E channels: ++p ≤ 0.005; +++p ≤ 0.001. Due to multiple comparisons, significance was set at p ≤ 0.005.