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. 2009 May 18;4(5):e5587. doi: 10.1371/journal.pone.0005587

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
1CC+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
1C1CC+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 Vα1C1CC+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.