M. Mund

This study shows that CGlcN is metabolized into carba-metabolites that inhibit bacterial cell wall synthesis, revealing a new antimetabolite mechanism of action.

The paper develops a MAD7-based genome editing system for E. coli to efficiently generate SNPs and gene deletions, demonstrating its utility in industrial strain engineering.

The paper uses superresolution microscopy to show clathrin coats partially assemble on flat membranes before bending, and introduces a model to explain this process.

LocMoFit is an open-source framework that fits models to SMLM data using maximum likelihood estimation to extract biological insights from single-molecule localization coordinates.

The paper identifies an autoinhibitory mechanism that limits actin assembly to specific synaptic endocytic events by regulating interactions between Nwk, Dap160, and WASp.

This study shows type-I myosins promote actin polymerization to drive membrane bending during endocytosis in budding yeast.

The paper uses genome-edited cell lines with labeled nuclear pore complexes to serve as reference standards for quantitative superresolution microscopy.

This paper develops a method to correct depth-induced aberrations in 3D single-molecule localization microscopy by using an imperfect PSF model and post-processing error correction.

The paper uses high-throughput superresolution microscopy to analyze endocytic protein organization in yeast, revealing a WASP nano-template that enhances actin nucleation efficiency during vesicle formation.

The paper introduces a fast and precise 3D localization method for arbitrary PSFs, achieving high resolution and speed on standard microscopes.