Michael Stadlmeier

This paper demonstrates that a quadrupole-ion trap instrument can perform multiplexed shotgun proteomics with accuracy comparable to a dedicated tribrid instrument, offering a cost-effective alternative.

The paper demonstrates that super-resolution mass spectrometry with least-squares fitting enables highly-multiplexed, accurate, and precise shotgun proteomics at the MS2 level.

The paper identifies that differential nuclear import timing controls gene expression onset in early embryonic development by regulating protein access to the genome.

The paper quantifies protein turnover in E. coli under 12 conditions, revealing cytoplasmic protein recycling under nitrogen limitation and identifying unknown proteolysis pathways.

This paper introduces TMTProC, an optimized complementary ion quantification method for TMTPro tags, improving sensitivity and accuracy in multiplexed proteomics.