Falk Schneider

This paper evaluates cross-talk between fluorescent proteins and NADH FLIM, identifying compatible FPs and providing a pipeline to manage cross-excitation in metabolic imaging.

The paper develops an FCS excitation scan assay to compare fluorescent reporters' brightness and photobleaching in tissue culture and zebrafish embryos, finding mNeonGreen outperforms mEGFP.

The paper describes the creation of StayRose, a red-shifted variant of StayGold using genetic code expansion, which retains photostability and can be monomerised.

The paper uses live-cell imaging and mathematical modeling to study PRLR internalization dynamics and their impact on signaling in pancreatic β-cells.

The paper introduces far-red chemigenetic kinase activity biosensors enabling five-color multiplexing, 4D imaging, and super-resolution via STED microscopy.

The paper uses single-cell phenomics to study DVE cell migration in mouse embryos, revealing mechanical heterogeneities and how surrounding cells facilitate collective migration.

This paper optimizes processing and analysis of scanning FCS data, introducing FoCuS-scan software and addressing bias and variance in diffusion measurements.

The paper measures diffusion dynamics of lipids and GPI-anchored proteins in actin-free plasma membrane vesicles using STED-FCS, showing actin cortex influences diffusion modes.