FCET is extended into the domain of receptor dynamics by the detection of polarized components of the 3 intensities.
Cell-by-cell distributions of FRET-fraction and rotational characteristics of the donor, and κ2 are available in parallel.
“Polarized FRET-indices” made from FRET efficiency and anisotropies are introduced for detecting conformational changes.
The existence of a receptor trimer is shown by decreasing homo-FRET between two donors by an acceptor (homo-FRET relief).
Monitoring triple-anisotropy correlations also in those cases when FRET actually does not occur, e.g. beyond R0.