Dual-Laser Tetra-Polarization FRET (4polFRET) for Site-Selective Control of Homo-FRET in Hetero-FRET Systems on the Cell Surface: The Homo-FRET Gate
László Bene, Miklós Bagdány, Tamás Ungvári, László Damjanovich
Abstract
László Bene, Miklós Bagdány, Tamás Ungvári, László Damjanovich
Abstract
The effects of donor homo-Förster resonance energy transfer (homo-FRET) taking place in hetero-FRET systems is described in the context of hetero-FRET detection via donor and acceptor fluorescence anisotropies in cell surface receptor clusters. Donor homo-FRET can influence both the efficiency of detection as well as the magnitude of the detectable hetero-FRET. A 4-fold polarized FRET detection scheme—tetrapolarization FRET (4polFRET)—is proposed not only for discriminating the effects of homo-FRET from those of hetero-FRET, but also for correlating homo-associations of the donors and acceptors at different donor–acceptor distances, even beyond the critical Förster distance for hetero-FRET ( R 0 ). The method is based on suppressing homo-FRET at the donor side with red-edge excitation. After the anisotropy effects of physical rotation and homo-FRET were separated by site-selective spectroscopy, the magnitude of the effect of homo-FRET on hetero-FRET has been estimated. It has been found significant, offering a new sensitive technique for detecting conformational dynamics via the homo-FRET mediated component of hetero-FRET, the “homo-FRET enhanced hetero-FRET” or “homo-FRET gate”. The method is realizable in flow, as well as in image cytometry equipped with polarization detecting facility.
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The effects of donor homo-Förster resonance energy transfer (homo-FRET) taking place in hetero-FRET systems is described in the context of hetero-FRET detection via donor and acceptor fluorescence anisotropies in cell surface receptor clusters. Donor homo-FRET can influence both the efficiency of detection as well as the magnitude of the detectable hetero-FRET. A 4-fold polarized FRET detection scheme—tetrapolarization FRET (4polFRET)—is proposed not only for discriminating the effects of homo-FRET from those of hetero-FRET, but also for correlating homo-associations of the donors and acceptors at different donor–acceptor distances, even beyond the critical Förster distance for hetero-FRET ( R 0 ). The method is based on suppressing homo-FRET at the donor side with red-edge excitation. After the anisotropy effects of physical rotation and homo-FRET were separated by site-selective spectroscopy, the magnitude of the effect of homo-FRET on hetero-FRET has been estimated. It has been found significant, offering a new sensitive technique for detecting conformational dynamics via the homo-FRET mediated component of hetero-FRET, the “homo-FRET enhanced hetero-FRET” or “homo-FRET gate”. The method is realizable in flow, as well as in image cytometry equipped with polarization detecting facility.
Key concepts: Förster resonance energy transfer, Chemistry, Fluorescence anisotropy, Acceptor, Fluorescence, Biophysics, Physics, Optics