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. Author manuscript; available in PMC: 2018 Jan 21.
Published in final edited form as: Cell Calcium. 2017 May 15;66:1–9. doi: 10.1016/j.ceca.2017.05.008

Fig. 6.

Fig. 6

Phosphorylation at sites S763 and S860 of CaV 1.3α1 subunit influences channel functional expression. A) Representative traces of Ba2+ currents recorded from HEK-293 cells expressing DPM mutant channels in absence and presence of 8-Br-cGMP (1 mM) plus 10 nM Calyculin A. B) Average current density-voltage relationships for IBa from HEK-293 cells expressing the wild-type CaV 1.3 channel and its double phosphorylation mutant (DPM) variant in the control condition and after incubation with 1 mM 8-Br-cGMP plus 10 nM Calyculin A (C). IBa density was calculated at a series of test pulses applied from a Vh of −80 mV in 5 mV steps between −70 and 30 mV.