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. 2021 Aug 9;108(9):1692–1709. doi: 10.1016/j.ajhg.2021.07.007

Table 3.

Summary of physiological parameters for homomeric wild-type and mutant GluK2 KARs

GluK2 constructs Deactivation (ms) Desensitization (ms) Degree of desensitization (%) Recovery (s) Glutamate EC50(μM) Peak amplitude (−nA) Surface localization (%)
Wild-type 2.5 ± 0.1 4.9 ± 0.2 100 ± 0 0.8 (0.7–0.9) 295 8.2 ± 0.6 85 ± 3
p.Ala657Thr 212 ± 82 (p = 0.011) 18 ± 1 (p < 0.001) 91 ± 1 (p < 0.0001) 0.5 (0.4–0.6) 47 (11–179) 1.4 ± 0.2 (p < 0.0001) 51 ± 5 (p < 0.0001)
p.Thr660Lys 260 ± 14 (p = 0.002) 8.9 ± 0.2 (NS) 57 ± 1 (p < 0.0001) 0.5 (0.2–0.9) 19 (15–26) 0.65 ± 0.08 (p < 0.0001) 16 ± 5 (p < 0.0001)
p.Thr660Arg 183 ± 27 (p = 0.023) 9.6 ± 1.6 (p = 0.009) 75 ± 1 (p < 0.0001) 0.9 (0.4–1.4) 52 (38–73) 1.9 ± 0.2 (p < 0.0001) 12 ± 6 (p < 0.0001)
p.Ile668Thr 1.5 ± 0.1 (NS) 1.7 ± 0.1 (NS) 98 ± 0.5 (NS) 2.4 (2.1–2.8) 3700 (2,300–10,800) 0.16 ± 0.02 (p < 0.0001) 91 ± 1 (NS)

τ values from fits to the data are given for deactivation, desensitization, and recovery from desensitization as described in the text. The data are expressed as mean ± SEM. Statistical information is given where significantly different from wild-type GluK2 receptors, except for 95% confidence intervals shown for recovery from desensitization and for the EC50 values. NS, not significant.