News

We are delighted to announce that our latest MRC PPU group leader, Chiara Maniaci, has now opened her laboratory.

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Tom Williams, who has been working as a postdoctoral researcher in Adrien Rousseau’s group since 2019 has been awarded the British Society for Cell Biology (BSCB) postdoctoral researcher medal for 2023.

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For many years, it has thought that eight types of ubiquitin chain can be formed in cells in which the C-terminal carboxylate of ubiquitin forms isopeptide bonds with the ε-amino group of any of the seven lysine residues in another ubiquitin molecule or a peptide bond with the α-amino group of the N-terminal methionine residue of another ubiquitin (Met1-linked ubiquitin).

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Dr. Mahima Swamy from the Medical Research Council Protein Phosphorylation and Ubiquitylation Unit (MRC-PPU) in the University of Dundee has been chosen to join the prestigious EMBO Young Investigator network, recognizing her as one of the rising stars in biology in Europe.

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Dr Greg Findlay and Professor Satpal Virdee, Principal Investigators in the MRC Protein Phosphorylation and Ubiquitylation Unit, have been awarded Wellcome Discovery Awards. The 8-year funding that totals ~£4.2M will support their research in Intellectual Disability and E3 ligase enzymes, respectively.

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Nick Brewer, Ian Ganley, and Yogesh Kulathu have been promoted to Personal Chair (Professor) as part of the 2022 Annual Review process for academic staff.

Nick Brewer

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On November 7 of this year, the Parkinson’s UK’s leadership team including CEO Caroline Rassell, Deputy director of research Professor David Dexter and the new Scotland director James Jopling visited the Parkinson’s research team at the University of Dundee. In the morning, researchers from Dundee including Professor Dario Alessi, Dr. Paul Davies, Professor Miratul Muqit, Dr.

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Mitochondria and peroxisomes are key eukaryotic metabolic organelles. They perform essential and related roles including fatty acid metabolism and ROS (Reactive Oxygen Species) scavenging.

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Discovered only in 2004, UFM1 is the most recently identified Ubiquitin-like protein. Like ubiquitin, UFM1 is post-translationally attached to proteins via an enzymatic cascade. Ribosomes located at the endoplasmic reticulum, the large molecular machines that carry out protein synthesis, are the main cellular targets of UFM1 attachment.

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Targeted protein degradation has become an exciting new drug modality. Tens of small molecule degraders, including proteolysis-targeting chimeras (PROTACs), have entered clinical trials to treat many different diseases.

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