Matthias Meurer

This paper introduces a chromosomally integrated yeast surface display system for scalable, quantitative antibody profiling and serological assays.

The paper improves CRISPR-Cas12a-assisted gene tagging in mammalian cells by enhancing HDR efficiency and reducing off-target integrations through modified cassettes and repair pathway modulation.

The paper introduces CASTLING, a method for efficiently creating pooled yeast gene tagging libraries using CRISPR/Cas12a and recombineering, achieving high tagging success rates.

The paper describes a C-SWAT library for high-throughput tagging of yeast ORFs and validates it by tagging the yeast proteome with fluorescent proteins.

The paper characterizes the MAL32 promoter in S. cerevisiae, showing its inducibility by maltose and distinct kinetics compared to the GAL1 promoter, and provides tools for its use.

This study evaluates how green fluorescent protein (greenFP) maturation kinetics and proteasomal degradation affect tandem fluorescent protein timers (tFTs), identifying greenFPs that degrade efficiently and guidelines for tFT design.