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. 2015 Aug 7;10(8):e0135191. doi: 10.1371/journal.pone.0135191

Table 1. Functional characteristics of the ASIC1a constructs.

wt ΔCCt V74C Y426C G430C G433C
INa (μA) 55.33±26.88 45.06±20.6 2.9±2.4** 22.65±14.22 22.75±14.73 3.6±3.8 **
pH0.5 6.35±0.02 6.35±0.014 6.36±0.04 6.57±0.01 6.36±0.01 6.55±0.02
IC50 (μM) amiloride 219±43 150±24 7.1±1.4 31.9±4.2 35.3±4.9 2.5±0.51
IC50 Cd2+ (mM) 0.527±0.049 1.16±0.095 < 0,01 0.032±0.0016* 0.010±0.001* 0.057±0.0037*
INa + BMOE (% of control) ND 90.2±10.0 115.7±24 6.4±0.18** 9.5±0.17** 89.1±13.3
INa (μA) +DTT ND 38.04±15.24 25.84±15.72 29.92±16.8 26.29±19.37 3.79±2.92

ASIC1a currents (INa) were elicited at pH 6.0. ΔCCt denotes ASIC1a mutant lacking the cysteines in the C-terminus. BMOE (2mM), Cd2+ and DTT (10 mM) were added in the extracellular medium.

** denotes statistical significance p<0.01 and

* p<0.05, unpaired t-test for the mutant compared to ASIC1a wt. denotes p<0.01 for treated versus untreated condition.

Current values (μA or % of control) are expressed as mean ± SD

IC0.5 and pH0.5 are expressed as best-fit values ± 95% confidence intervals of at least 4 independent experiments