We are developing a new method for spatial manipulation of light at the nanoscale by assembly of plasmonic nanostructures. We aim to use this method to advance visualization of densely packed biomolecules and their dynamics.
Metal nanostructures are capable of massive enhancements of optical response, which arise from collective electromagnetic resonances called plasmons. The interaction of a fluorophore and a plasmonic structure strongly increases the number of emitted photons. Recently emerging methods of superresolution microscopy allowed to discover previously inaccessible aspects of plasmonic enhancement. It appears that besides the increase in number of emitted photons, plasmonic enhancement also affects the projected position and direction of the fluorophore-emitted photons in surprising and puzzling ways. We are studying how to control these shifts by altering the enhancement mechanism, fluorophore-plasmon distance, and their dynamics.
We combine methods from different fields
We are using DNA self assembly to position fluorophores and plasmonic nanostructures at defined distances.
Single molecule localization microscopy enables us to study the shifts in the direction of emission below the diffraction limit. Suspendisse eu.
We use machine learning to to describe and reconstruct sub-diffraction limited shifts in the projection of plasmon-coupled fluorophores.