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. 2018 Oct 24;38(43):9215–9227. doi: 10.1523/JNEUROSCI.0695-18.2018

Figure 8.

Figure 8.

The unstructured region of Stac1 (residues 168–285), which links the PKC C1 and SH3_1 domains, is sufficient to suppress calcium-dependent inactivation of CaV1.2. A, Schematic representation and domain architecture of full-length mouse Stac1 (residue numbers adapted from UniProt). BF, for tsA201 cells transfected with CaV1.2, β2a, α21, and the indicated Stac1 construct. The top row illustrates representative peak currents carried by Ca2+ (red, vertically scaled by indicated factors, test potential of +30 mV except +20 mV for D) or Ba2+ (black, test potential of +10 mV), the middle row shows the fraction of peak current remaining 150 ms after the peak (R150) as a function of test potential, and the bottom row illustrates the peak I–V relationships. Scale bars: 10 pA/pF (unscaled Ba2+ currents, vertical), 50 ms (horizontal). Figure 8-1 and Figure 8-2 show that the region linking the PKC C1 and SH3_1 domains of both Stac2 and Stac3, respectively, is also sufficient to completely suppress calcium-dependent inactivation. Figure 8-3 shows that smaller, N- or C-terminal segments of this region either do not, or only partially, suppress calcium-dependent inactivation.