From small molecules to complex organelles
- September 11, 2023 SPOP targets the immune transcription factor IRF1 for proteasomal degradation In work recently published in eLife, the Versteeg lab (Max Perutz Labs) has identified a factor essential for the degradation of the transcription factor IRF1, a key driver of the innate immune response.
- July 7, 2023 Cryo-EM structure of the chain-elongating E3 ubiquitin ligase UBR5 Zuzana Hodakova, David Haselbach (IMP) and their collaborators used cryo-electron microscopy to analyse the structure of the enzyme UBR5. Difficult to work on due to its size, UBR5 is important due to its role in marking proteins for degradation. The findings were now published in EMBO Journal.
- June 6, 2023 Aggrephagy at a glance In their Review published in the Journal of Cell Science, Bernd Bauer, Sascha Martens and Luca Ferrari (Max Perutz Labs), present the molecular mechanisms of aggrephagy and discuss aggrephagy pathways in neurons and implications in disease and therapy.
About the Program
Targeted Protein Degradation: From small molecules to complex organelles
Our Special Research Program is a collaborative research platform to unravel how proteins are targeted for degradation. We focus on the two major cellular proteolytic pathways, the ubiquitin-proteasome system (UPS) and autophagy, and the crosstalk between them in the cytoplasm and in the nucleus. Furthermore, we investigate how small molecules can be used to chemically reprogram the degradation systems, enabling the targeted proteolysis of selected proteins in a spatially and temporally controlled manner …
- 2023 Structural basis of how the BIRC6/SMAC complex regulates apoptosis and autophagy Science Go to publication →
- 2023 Shuffled ATG8 interacting motifs form an ancestral bridge between UFMylation and C53-mediated autophagy EMBO Journal Go to publication →
- 2022 Functional E3 ligase hotspots and resistance mechanisms to small-molecule degraders Nature Chemical Biology Go to publication →