Brandon Ho

The paper identifies Rad53-dependent protein localization changes during replication stress, revealing Mec1-independent activation of Rad53 in yeast.

This study develops a yeast whole-cell biocatalyst expressing MHETase for PET degradation, showing comparable activity to purified enzyme and stability under various conditions.

The paper quantifies protein localization dynamics in yeast during DNA replication stress, revealing phenotypic heterogeneity and previously undetected re-localization events.

The paper introduces BFG-GI to map DNA damage-dependent genetic interactions in yeast by combining party mating and barcode fusion genetics, revealing new condition-specific interactions.

This study normalizes and compares 19 yeast proteomic datasets to estimate absolute protein abundance and assess measurement variability across stress conditions.