From molecular logic to therapeutic modulation: advances in Ub/UBL signalling
Ubiquitin (Ub) and ubiquitin-like proteins (UBLs) are central regulators of cell signalling, with roles spanning proteasomal degradation, immune defence, DNA repair, autophagy, and the stress response. Their conserved β-grasp fold provides a remarkably versatile protein architecture that can be redeployed across diverse signalling pathways and modulated in disease contexts. Conjugation and removal through dedicated E1-E2-E3 and protease systems generate a rich regulatory code, further diversified by chain topology, hybrid architectures, and emerging non-canonical modifications. This special issue highlights recent advances in Ub and UBL biology, from specialised UBL pathways to host-pathogen interactions and non-protein conjugation events, as well as translational applications such as targeted protein degradation. Together, these reviews showcase the breadth, adaptability, and therapeutic potential of these small but powerful modifiers.
Authors
- Chiara Maniaci (ORCID: https://orcid.org/0000-0001-7887-7388)
- Benjamin M. Foster (ORCID: https://orcid.org/0000-0003-0670-2321)
Institutions
- MRC Protein Phosphorylation and Ubiquitylation Unit (GB)
- Cancer Research UK Manchester Institute (GB)
Publication Details
- Journal
- Essays in Biochemistry
- Published
- 2025-12-01
- DOI
- https://doi.org/10.1042/ebc20250062
- Primary Topic
- Ubiquitin and proteasome pathways
- Type
- article
- Field-Weighted Citation Impact
- 0.00