Marina S. Dietz

This study uses DNA-PAINT to quantitatively map nanoscale EGFR-Grb2 assemblies in cells after EGF stimulation, revealing changes in EGFR density and Grb2 accumulation.

This paper introduces a wash-free method for multi-target super-resolution microscopy using photocaged DNA labels, demonstrating improved imaging accuracy without sample manipulation.

The paper uses single-molecule FRET and tracking to study MET receptor activation by InlB in living cells, finding a dimeric complex lifetime of ~1 second and slower diffusion for dimers.

This paper introduces Rho-tag and SiR-tag, fast, reversible, and fluorogenic protein tags for live-cell imaging, compatible with super-resolution techniques and demonstrated in zebrafish larvae.

This paper introduces a labeling method for long-term single-molecule tracking in living cells and demonstrates its application to study EGFR dynamics.

The paper introduces self-quenched fluorophore-DNA labels to reduce background signal in super-resolution microscopy, improving imaging performance in STED and SMLM.

The paper uses single-molecule imaging and molecular dynamics simulations to study early MET receptor activation in situ, revealing structural dynamics and a refined dimer model.