Radek Nowak (@RPNowak) header
Radek Nowak (@RPNowak) profile picture

Professor @UniBonn. Former @DanaFarber @harvardmed | Targeted Protein Degradation | Chemical and Structural Biology | @UniofOxford alumni. Tweets are my own.

Bonn, Germany
Joined November 2013
Photo by Radek Nowak (@RPNowak)Photo by Radek Nowak (@RPNowak)Photo by Radek Nowak (@RPNowak)Photo by Radek Nowak (@RPNowak)Photo by Radek Nowak (@RPNowak)Photo by Radek Nowak (@RPNowak)Photo by Radek Nowak (@RPNowak)Photo by Radek Nowak (@RPNowak)Photo by Radek Nowak (@RPNowak)Photo by Radek Nowak (@RPNowak)
Targeted protein #degradation: from mechanisms to #clinic. New molecular mechanisms can rapidly be translated - we can learn so much from nature. Great to be able to share this piece with @jonathanMtsai Ben Ebert and Eric Fischer @fischerlab1. #TPD nature.com/articles/s41580-0…
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NEW: today OpenBind ‘comes out of stealth’ so to speak with their first data dump of ~900 novel protein-ligand structures - most with paired affinities This represents a meaningful %-age increase in all of humanities P-L data in the PDB collected in the last 50 years More👇
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Radek Nowak retweeted
Nathanael Gray @StanfordUChem about bifunctional proximity-inducing molecules which allow to rewire transcription #AACR26. TCIPs hijacking BCL6, BRD4, CDK9, p300 and p53 Y220C as “synthetic hybride TFs” leading to transcriptional hyperactivation & gain-of-function pharmacology.
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📢 Save the Date for our DFCI Targeted Protein Degradation in-person Meeting!! 📍 Location: Boston, MA 📅 Date: September 10th, 2026 🔬 Talks from leaders in the field 🤝 Networking reception 🌍 Livestream available
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Induced proximity-based therapeutic modalities nature.com/articles/s41573-0… rdcu.be/eOfBH This new Review discusses the rapidly expanding landscape of therapeutic approaches based on inducing proximity between proteins, including targeted protein degraders and more
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Was so much fun to be part of that journey! So much for the exciting science and most importantly friendships. To the next 10! @fischerlab1
This month we celebrated a decade of the @fischerlab1 - 10 years of discovery, innovation, and collaboration! Thank you to everyone who’s been part of this journey — past and present lab members, collaborators, and supporters. Here’s to the next 10! 🧪🎉
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Excited to present our research at the Promega TPD and Induced Proximity Summit this Thursday! #TPD #UniBonn promega.foleon.com/na-tpd-sy…
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Excited to share our discovery of potent TRIM21 molecular glues with anticancer activity, online today @CD_AACR: "Defining the antitumor mechanism of action of a clinical-stage compound as a selective degrader of the nuclear pore complex". 1/18
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A new study in @MolecularCell by @DanaFarber’s @biomiko, Benjamin Ebert, MD, PhD, and @fischerlab1 reports a systematic screen of 9,000 zinc fingers revealing 38 new CRBN-recruited degrons. This includes targets invisible to proteomics, expanding the ZF proteome map to guide drug design and mitigate off-target toxicity. Read more: bit.ly/41XoG1Q
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Thanks to all co-authors: @jeanniescience Simran Rastogi, Anna Goldstein, ​ Marek Nagiec, Kathrine Donovan, Jianwei Che, Moritz Hunkeler, Chi-Lin Hsu, Megha Lakshminarayan, Chelsea Shu @beckyzon @zkozicka Paul Park @jonathanMtsai @hojong_yoon @LynJonesChemBio @adamssperling
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This work was a fantastic collaboration: 🔬Structure: @jihojasonpark, @RPNowak, @ssroyburman - @fischerlab1 🧬 Functional Genomics: JessePellman, CharlesZou - Ebert lab ⚗️Chemistry: Hlib Razumkov, Qixiang Geng (Gray lab)
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A single ZF residue can switch a drug’s specificity. That’s a lever for rational molecular‑glue design.
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Chemistry rewires biology: subtle changes to glutarimide analogs reshape degron selectivity, reprogramming CRBN toward new ZF targets.
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Structure + mutagenesis reveal distinct CRBN recruitment modes—different substrates or drugs interact with different CRBN surfaces.
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CRBN is more versatile than expected: potent degraders can overcome β-hairpin mutations and still engage substrates.
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Degron profiling reveals hidden off-targets: OSR1 is not detected in proteomics experiments, yet emerges as a CRBN substrate. OSR1 plays a critical role in kidney development—highlighting potential clinical implications.
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