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. Author manuscript; available in PMC: 2019 Jul 1.
Published in final edited form as: Mov Disord. 2018 Apr 11;33(6):992–999. doi: 10.1002/mds.27315

Table 1.

Summary of pharmacological data

Measurement WT GluN2A GluN2A-A643D p value
Mean 95% CI n Mean 95% CI n
Glutamate EC50, μM 5.0 (4.1, 6.1) 18 1.0 (0.7, 1.4) 23 <0.0001
Glycine, EC50, μM 1.1 (0.9, 1.5) 10 0.11 (0.09, 0.13) 13 <0.0001
Mg2+, IC50, μM 18.6 (12.9, 27.0) 13 39.4 (27.5, 56.2) 12 0.004
Proton, % A 42.8 (40.5, 45.0) 8 48.0 (45.1, 50.9) 13 0.010
Zn2+, IC50, nM 9.1 (6.6, 12.4) 12 30.3 (12.7, 72.3) 11 0.007
Zn2+, Residual Current (%)B 30.9 (24.3, 37.4) 12 67.3 (60.7, 73.9) 11 <0.0001
A

% current remaining measured at pH 6.8 compared to pH 7.6 at maximal L-glutamate and glycine activation

B

current remaining in maximum Zn2+ concentration (expressed as % of maximal receptor activation in the absence of Zn2+)

p value determined by unpaired t-tests (GraphPad Prism 5.0) comparing WT vs. mutant receptors. For EC50 and IC50 measurements log values were used for statistical comparison.

n = the number of oocytes evaluated for the measured endpoint.

CI = confidence interval