The α2δ-1 subunit remodels CaV1.2 voltage sensors and allows Ca2+ influx at physiological membrane potentials
journal contributionposted on 12.03.2019 by Nicoletta Savalli, Antonios Pantazis, Daniel Sigg, James N. Weiss, Alan Neely, Riccardo Olcese
Any type of content formally published in an academic journal, usually following a peer-review process.
Excitation-evoked calcium influx across cellular membranes is strictly controlled by voltage-gated calcium channels
(CaV), which possess four distinct voltage-sensing domains (VSDs) that direct the opening of a central pore.
The energetic interactions between the VSDs and the pore are critical for tuning the channel’s voltage dependence.
The accessory α2δ-1 subunit is known to facilitate CaV1.2 voltage-dependent activation, but the underlying
mechanism is unknown. In this study, using voltage clamp fluorometry, we track the activation of the four
individual VSDs in a human L-type CaV1.2 channel consisting of α1C and β3 subunits. We find that, without α2δ-1,
the channel complex displays a right-shifted voltage dependence such that currents mainly develop at nonphysiological
membrane potentials because of very weak VSD–pore interactions. The presence of α2δ-1 facilitates
channel activation by increasing the voltage sensitivity (i.e., the effective charge) of VSDs I–III. Moreover, the α2δ-1
subunit also makes VSDs I–III more efficient at opening the channel by increasing the coupling energy between
VSDs II and III and the pore, thus allowing Ca influx within the range of physiological membrane potentials.