E. D'Este

The paper introduces exchangeable HaloTag ligands for multi-modal super-resolution fluorescence microscopy, enabling dual-color imaging techniques like PAINT and STED.

This paper introduces a method to create caging-group free photoactivatable fluorophores for live-cell nanoscopy, demonstrating their utility in multiple superresolution techniques.

This paper develops a 4Pi-STORM microscope with dynamic spline PSF models to achieve high 3D resolution and accuracy in single molecule localization microscopy.

This paper describes a method to systematically tune the spirocyclization equilibrium of rhodamines to create probes for different super-resolution microscopy techniques.

The paper quantifies dendritic spine size and shape changes using time-series analysis and proposes a biophysical model showing actin self-organization into a critical state.

The paper develops fluorescent actin probes that overcome efflux by plasma membrane pumps, enabling effective staining in multiple organisms and cell types without inhibitors.

The paper introduces SBG-conjugated fluorophores to improve extracellular labeling of SNAP-fused proteins, enabling precise analysis of GPCR populations in living cells and tissues.

The paper introduces LUXendin peptides that label and visualize endogenous GLP1R with high specificity, revealing receptor organization and dynamics.