Ben De Clercq

Learn More
We perform second-harmonic generation (SHG) microscopy with circularly polarized (CP) light to measure chirality of individual twisted-cross gold nanodimers. The chiral signatures, based on different SHG response for the two CP components of incident light, are clearly visible even with off-resonance excitation. The SHG responses of individual nanodimers(More)
Many membrane proteins and lipids are partially confined in substructures ranging from tens of nanometers to micrometers in size. Evidence for heterogeneities in the membrane of oligodendrocytes, i.e. the myelin-producing cells of the central nervous system, is almost exclusively based on detergent methods. However, as application of detergents can alter(More)
Single particle tracking (SPT) of transmembrane receptors in the plasma membrane often reveals heterogeneous diffusion. A thorough interpretation of the displacements requires an extensive analysis suited for discrimination of different motion types present in the data. Here the diffusion pattern of the homomeric alpha3-containing glycine receptor (GlyR) is(More)
Nonlinear optical imaging is a powerful method for observing bulk and interfacial phenomena in time and space. Here, we present a step-by-step description of how to carry out second harmonic generation imaging with a kHz amplifier laser system and demonstrate its applicability for SHG microscopy studies of highly size-resolved colloidal CdSe quantum dots(More)
Fluorescence recovery after photobleaching (FRAP) is a common technique to probe mobility of fluorescently labeled proteins in biological membranes by monitoring the time-dependence of the spatially integrated fluorescence signals after a bleaching pulse. Discrimination by FRAP between free diffusion with an immobile fraction (FDIM) and the phenomenological(More)
  • 1