Table 1. Intra- and intermolecular distances between the Cav1.2 calcium channel α1C and β subunits measured by three-color FRET microscopy.
Channel subunits | Measured distances (r) | β1b | β2d | β3 | ||
r, Å | r, Å | c | r, Å | c | ||
Vα1CC+Rβ | r C-V | 68±1 (17) | 68±2 (13) | 0.90±0.37 | 69±1 (19) | 0.60±0.05 |
r C∼V | 72±3 (5) | 1.27±0.54 | 77±3 (6) | 1.16±0.17 | ||
r V-R | 95±3 (13) | 99±3§ (8) | 1.70±0.27 | 90±2 (19) | 0.97±0.20 | |
r V∼R | 107±1 (3) | 2.52±0.17 | 100±2 (15) | 1.72±0.23 | ||
r C-R | 85±2‡ (13) | 84±2 (13) | 79±1 (14) | 0.70±0.10 | ||
r C∼R | 85±1 (10) | 1.55±0.07 | ||||
Vα1C+α1CC+Rβ | r C∼V | 67±1* (26) | 72±2 (13) | 79±4 (10) | ||
r V-R | 90±2 (26) | 90±2 (13) | 90±5 (10) | |||
r C-R | 78±1† (26) | 86±2 (6) | 80±4 (8) |
P<0.002 vs. β3.
P<0.05 vs. β2d.
P<0.05 vs. β3.
P<0.05 vs. r V-R in Vα1C+α1CC+Rβ2d.
FRET efficiency between the indicated fluorophores fused to the α1C and β1b, β2d or β3 subunits was measured in the plasma membrane of expressing COS1 cells and fitted to a Gaussian function. In cases when the routine curve fit showed two significantly different Gaussian distributions, the corresponding dispersion coefficients c (mean±SEM) are shown for both distances (see Experimental Procedures). V – mVenus, C- mCerulean, R – tagRFP. Shown values of r are mean±SEM. Number of cells is shown in parentheses.