Table 1.
Colocalization of filamin, CFTR, and RACK1 in Calu-3 cells
| Protein1 | Protein2 | Rpearson | Roverlap | M1 | M2 | ICQ | n (cells) |
|---|---|---|---|---|---|---|---|
| Filamin | CFTR | 0.61 ± 0.04 | 0.71 ± 0.06 | 0.28 ± 0.06 | 0.57 ± 0.07 | 0.35 ± 0.05 | 12 (130) |
| Filamin | RACK1 | 0.70 ± 0.06 | 0.79 ± 0.04 | 0.39 ± 0.06 | 0.57 ± 0.04 | 0.37 ± 0.02 | 6 (47) |
| CFTR | RACK1 | 0.50 ± 0.03 | 0.60 ± 0.03 | 0.24 ± 0.04 | 0.35 ± 0.04 | 0.29 ± 0.04 | 8 (80) |
All values shown are means ± SE. CFTR, cystic fibrosis transmembrane regulator; RACK1, receptor for activated C kinase 1; Rpearson, Pearson's correlation coefficient (−1; negative correlation, e.g., exclusion; 0: no correlation; 1: positive correlation); Roverlap, overlap correlation coefficient, similar to Pearson's coefficient but without subtraction of the mean intensity values in each channel (0: negative correlation; 1: positive correlation); M1 and M2: Manders coefficients, quantifying the fractional intensity overlap of the first protein's immunofluorescence signal with that of the second protein (M1) and vice versa (M2); ICQ, intensity correlation quotient, as defined by Li et al. (Ref. 6; −0.5: exclusion; 0: random with uncorrelated intensities; 0.5: colocalization with completely correlated intensities between the 2 channels); n (cells): n, total number of imaged fields; cells, total number of cells in these fields