Table 1.

Biophysical properties and G-protein modulation of calcium channel α1 subunits

Systemα1Bα1E(rbEII)α1Elongα1bEEEEα1BΔN1–55
IBa slope conductance (μS)Oocytes36.6  ± 3.3 (7)17.6  ± 3.4 (8)15.6  ± 3.9 (7)10.7  ± 1.1 (7)28.1  ± 3.1 (15)
V50 for control IBa activation (mV)Oocytes−8.5  ± 1.3 (7)−1.2  ± 1.7 (8)0.2  ± 1.4 (7)2.8  ± 0.7 (7)−5.3  ± 1.8 (7)
V50 forIBa activation plus quinpirole (mV)Oocytes−1.0  ± 1.7* (7)−0.8  ± 1.5 (8)3.8  ± 1.3* (7)7.0  ± 0.9* (7)−6.2  ± 1.8 (7)
% inhibition by quinpirole at 0 mVOocytes49.6  ± 3.0 (13)−3.7  ± 1.5** (11)25.8  ± 1.5** (14)30.2  ± 3.6** (9)−1.1  ± 0.9** (18)
Maximum controlIBa (+GDPβS) (pA.pF−1)COS-724.4  ± 4.3 (5)26.1  ± 5.2 (5)17.9  ± 3.4 (7)22.3  ± 3.7 (7)26.5  ± 6.1 (15)
τact in control cells (+GDPβS) at −10 mV (msec)COS-77.9  ± 1.9 (5)4.6  ± 0.6 (5)3.3  ± 0.4 (7)6.5  ± 1.2 (7)7.7  ± 1.3 (15)
τact with Gβ1γ2 at −10 mV (msec)COS-733.6  ± 4.6 (9)7.0  ± 1.1** (6)16.7  ± 1.6** (10)18.4  ± 1.8** (10)6.3  ± 0.7** (5)
Facilitation by depolarizing prepulse (P2/P1 at −10 mV)COS-75.3  ± 2.0 (8)1.0  ± 0.1** (8)1.8  ± 0.6** (7)1.9  ± 0.3** (8)1.1  ± 0.03** (5)
  • The parameters determined for the different α1 constructs (co-transfected with β2a and α2-δ) were measured as described in Materials and Methods, and in the legends to Figures 2 and 3. The statistical significances of the differences between the V50 data for the I–V plots in the presence and absence of quinpirole were determined by paired t test, *p < 0.005. The data for quinpirole inhibition ofIBa were determined from time course studies at 0 mV. The statistical significance of the differences in % inhibition by quinpirole, τact in the presence of Gβ1γ2, and facilitation ratio in the presence of Gβ1γ2, for all the constructs compared with α1B, is indicated by **p < 0.01 (Student’s t test). There are no statistically significant differences between α1Elong and α1bEEEE for these parameters (p > 0.05). The differences between other parameters, not relating to G-protein modulation, were not examined.