Mirosław Tarnawski

This paper introduces a giant vesicle platform to study synthetic ER networks, showing that lipid composition and GTPase Sey1 influence network formation and structure.

The paper introduces CLIP-tag2, an engineered variant of the CLIP-tag protein that significantly improves labeling speed and efficiency for live-cell imaging.

The paper develops two variants of a glutamate indicator with enhanced sensitivity and tailored deactivation rates for studying synaptic transmission in vivo.

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 SNAP-tag2, an improved version of SNAP-tag with faster labeling kinetics and higher fluorescence brightness for better live-cell imaging.

The paper demonstrates that echinenone-functionalized OCP requires two photons for photoprotection, revealing a sequential 2-photon absorption mechanism unique to a single biological photoreceptor.

This study uses MINFLUX to analyze kinesin-1 dynamics in neurites, identifying ATP-binding states and microtubule switching behavior.

This paper describes an engineered nanobody that modulates GFP binding with small molecules, enabling controlled study of GFP fusion proteins in biological processes.