Katherine Donovan

Lead Scientist / Managing Director-Fischer labs Dana Farber Cancer Institute

Katherine Donovan holds the position of Lead Scientist and Managing Director of Fischer labs within the Dana-Farber Cancer Institute/Harvard Medical School. Her doctoral research was conducted under Prof. Renwick Dobson at the University of Canterbury, New Zealand, with a focus on protein biochemistry and structural biology. Katherine’s postdoctoral work began in 2016 in Prof. Eric Fischer’s lab, where she cultivated a keen interest in proteomics – a technique she uses to measure protein expression changes in response to various stimuli. She established and managed proteomics groups within both Fischer Lab and the Center for Protein Degradation, specializing in degrader screening and target identification. Her work has been pivotal in detecting the degradation targets of several molecules, notably uncovering SALL4 as the potential key to thalidomide’s teratogenic effects. Katherine has co-headed extensive projects to delineate the degradable kinome and HDACome, and has launched a public degradation proteomics initiative to offer complimentary degrader target mapping to the scientific community. Her notable contributions to targeted protein degradation (TPD) research were honored with the Arvinas TPD Early Career Researcher Award in 2022. Presently, she supervises and actively contributes to various projects in ligase biology and protein degradation while managing the Fischer lab and TPD proteomics operations under the Chemical Biology Program.

Seminars

Monday 27th October 2025
Unveiling the Hidden Interactome of CRBN Molecular Glues with Chemoproteomics
9:30 am
  • Developed a scalable affinity purification mass spectrometry workflow for the identification of chemically glued targets
  • Screened 20 IMiD analogs and identified over 290 targets chemically recruited to CRBN. Targets were prioritized through computational alignment analysis
  • The novel nonZF target PPIL4 was validated and the new selective lead molecule identified through a biochemical screen of over 6,000 IMiD analogs
Katherine Donovan