Benjamin Luke Schulz

The paper develops a pipeline to collect, characterize, and scale wild yeast for beer brewing, identifying interventions to overcome industrial fermentation challenges.

The paper characterizes the yeast secretome under various proteosynthetic stress conditions and identifies BiP as a functional extracellular chaperone in specific stress scenarios.

This study investigates how influenza A virus infection alters host cell glycosylation, identifying changes in sialic acid levels and glycan structures, and linking these to viral mechanisms and host responses.

This paper identifies sequence determinants that regulate oligosaccharyltransferase (OST) catalytic efficiency and glycosylation specificity in proteins.

This study characterizes the proteome of brewers spent grain (BSG) and identifies key proteins, differential abundance, and safety concerns to guide downstream processing for functional food ingredients.

This study identifies trace-level cytokines in PASC patients linked to cardiovascular symptoms and shows their impact on cardiomyocyte function using nanotechnology detection.

This study compares fragmentation methods for glycopeptide analysis, finding CID identifies more glycopeptides while EAD improves site localization, and EAciD combines both benefits.

GlypNirO automates quantitative glycoproteomic analysis by integrating Byonic and Proteome Discoverer outputs, identifying glycosylation changes in hepatocellular carcinoma as potential biomarkers.

DIALib automates the creation of DIA ion libraries for peptides and glycopeptides, enabling unbiased analysis of glycoproteomes without prior glycan knowledge.

This study shows that increasing OST48 expression in diabetic mice improves insulin secretion but does not prevent diabetic kidney disease despite enhancing AGE clearance.

This study shows that increased podocyte expression of oligosaccharyltransferase-48kDa subunit worsens diabetic kidney disease by causing endoplasmic reticulum stress and kidney dysfunction.