Lina Riachy, Rodolphe Jaffiol, Cyrille Vézy,
Non-radiative Excitation Fluorescence Microscopy for Studying Membrane Adhesion at the Nanoscale
Focus On Microscopy 2017, Bordeaux 09/04/17-12/04/17
Indexed by
Non-Radiative Excitation Fluorescence Microscopy (NEFM) [1] constitutes a new way to observe biological samples beyond the diffraction limit. By coating a substrate with an homogeneous monolayer of quantum dots (QDs), Förster Resonance Energy Transfer (FRET) could be achieved between the QDs layer (which play the role of the donor) and Giant Unilamellar Vesicles (GUVs) labelled with DiD (which play the role of the acceptor). The dyes were not directly excited by the laser source but through a non-radiative energy transfer. GUVs were added on a QD layer coated with poly-L-lysine (electrostatic attraction occurred between the positively charged surface and negatively charged GUVs). On this kind of sample, we were able to observe at the same time the emission of the DiD and the quenching of the QDs (as shown in figure 1). It clearly indicates that non-radiative energy transfer occurs from the QDs to DiD. From these two pictures, we also calculated the distance between the lipid membrane and the surface for each pixel with a nanometric resolution. [1] P. Winckler, R. Jaffiol, J. Plain, and P. Royer. “Nanoradiative Excitation Fluorescence: Probing Volumes Down to the Attoliter Range.” The Journal of Physical Chemistry Letters 1, 2451-2454 (2010).