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. 2020 Jan 27;39(5):e102622. doi: 10.15252/embj.2019102622

Table 6.

Effect of α‐actinin‐1 ectopic expression on biophysical properties of CaV1.2 single‐channel currents

Gating parameter Availability (%) NPopen (%) Popen (%) I (Mean ensemble Avg.) [fA] Unitary current (pA) Sweeps n
WT (a) 56.6 ± 6.3 3.6 ± 0.75 3.4 ± 0.69 14.8 ± 3.1 0.89 ± 0.02 2,744 32–35
WT + α‐Actinin (b) 76.5 ± 6.2* 9.2 ± 2.0** 7.9 ± 2.0* 31.3 ± 7.5* 0.84 ± 0.02 2,388 23–25
WT + EE847/851KK (c) 32.9 ± 7.5**** 1.9 ± 0.7** 1.8 ± 0.7* 7.4 ± 2.8* 0.83 ± 0.03 1,252 13
K1647E + α‐Actinin (d) 43 ± 5.0 1.8 ± 0.3 1.7 ± 0.3 8.5 ± 1.5 0.83 ± 0.01 2,601 30
K1647E + EE847/851KK (e) 67.9 ± 6.9** 2.6 ± 0.5 2.5 ± 0.5 11.3 ± 2.7 0.84 ± 0.02 1,376 16
Unpaired t‐test a‐b¥ a‐b¥ a‐b¥ a‐b¥ NS
b‐c¥ b‐c¥ b‐c¥ b‐c¥
d‐e¥ d‐e P = 0.7 d‐e P = 0.7

HEK293 cells were transiently transfected with WT CaV1.2 (α11.2, α2‐δ1, and β2a) and, if indicated, with α‐actinin‐1 WT or E847K/E851K. Single‐channel activity was obtained as in Table 5. Statistical significance was determined by pairwise testing of CaV1.2 WT alone (a) versus CaV1.2 WT + α‐actinin WT (b), CaV1.2 WT + α‐actinin‐1 WT versus CaV1.2 + α‐actinin‐1 E847K/E851K (c), and CaV1.2 K1647E + α‐actinin‐1 WT (d) versus CaV1.2 K1647E + α‐actinin‐1 E847K/E851K (e) with an unpaired t‐test¥. Given are mean values ± SEM (*P < 0.05, **P < 0.01, ****P < 0.0001). Values for CaV1.2 WT are provided for comparison from Table 5.