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. Author manuscript; available in PMC: 2021 Feb 9.
Published in final edited form as: Biochemistry. 2020 Sep 10;59(38):3594–3614. doi: 10.1021/acs.biochem.0c00576

Table 1.

Pharmacological Parameters for the Proton Concentration-Response Curves in the Absence and Presence of Ca2+ and Mg2+ and EDTAa

receptor condition basal (%) Emax (%) potency (pH) Hill slope
GPR4 without Ca2+/Mg2+ 0 100 8.11 ± 0.01 5.90 ± 0.31
with 1 mM Ca2+/Mg2+ 7.0 ± 2.5 127.2 ± 2.3 8.08 ± 0.01 5.14 ± 0.50
GPR65 without Ca2+/Mg2+ 0 100 7.49 ± 0.01 4.31 ± 0.23
with 1 mM Ca2+/Mg2+ 0.0 ± 2.5 114.8 ± 3.2 7.48 ± 0.01 4.85 ± 0.52
GPR68 without Ca2+/Mg2+ 0 100 6.74 ± 0.01 2.31 ± 0.06
with 1 mM Ca2+/Mg2+ 2.3 ± 1.9 129.8 ± 2.6 6.81 ± 0.01 2.37 ± 0.16
GPR68 control 0 (shared globally) 98.2 ± 1.5 6.81 ± 0.01 2.66 ± 0.13
1 μM EDTA 96.5 ± 1.6 6.72 ± 0.01 2.62 ± 0.13
3 μM EDTA 94.8 ± 1.6 6.72 ± 0.01 2.64 ± 0.13
10 μM EDTA 104.3 ± 1.9 6.68 ± 0.01 2.63 ± 0.13
30 μM EDTA 103.1 ± 2.2 6.65 ± 0.01 2.56 ± 0.14
100 μM EDTA 100.5 ± 2.5 6.63 ± 0.01 5.23 ± 0.15
a

Concentration-response curves are presented in Figure 2. Parameters were retrieved from fittings with pooled and normalized results using the Prism 8.4 built-in four-parameter logistic function.