Half-calcified calmodulin promotes basal activity and inactivation of the L-type calcium channel CaV1.2
Peter H. Bartels, Ian Salveson, Andrea M. Coleman, David E. Anderson, Grace Jeng, Zoila M. Estrada‐Tobar, Kwun Nok Mimi Man, Qinhong Yu, Elza Kuzmenkina, Madeline Nieves‐Cintrón, Manuel F. Navedo, Mary C. Horne, Johannes Hell, James B. Ames
Abstract
The L-type Ca 2+ channel Ca V 1.2 controls gene expression, cardiac contraction, and neuronal activity. Calmodulin (CaM) governs Ca V 1.2 open probability (Po) and Ca 2+ -dependent inactivation (CDI) but the mechanisms remain unclear. Here, we present electrophysiological data that identify a half Ca 2+saturated CaM species (Ca 2 /CaM) with Ca 2+ bound solely at the third and fourth EF-hands (EF3 and EF4) under resting Ca 2+ concentrations (50-100 nM) that constitutively preassociates with Ca V 1.2 to promote Po and CDI. We also present an NMR structure of a complex between the Ca V 1.2 IQ motif (residues 1644-1665) and Ca 2 /CaM 12' , a calmodulin mutant in which Ca 2+ binding to EF1 and EF2 is completely disabled. We found that the CaM 12' N-lobe does not interact with the IQ motif. The CaM 12' C-lobe bound two Ca 2+ ions and formed close contacts with IQ residues I1654 and Y1657. I1654A and Y1657D mutations impaired CaM binding, CDI, and Po, as did disabling Ca 2+ binding to EF3 and EF4 in the CaM 34 mutant when compared to WT CaM. Accordingly, a previously unappreciated Ca 2 /CaM species promotes Ca V 1.2 Po and CDI, identifying Ca 2 /CaM as an important mediator of Ca signaling.