Molecular glues to stabilise protein-protein interactions.

Lorenzo Soini, Seppe Leysen, Jeremy Davis, Christian Ottmann
Author Information
  1. Lorenzo Soini: Laboratory of Chemical Biology, Department of Biomedical Engineering and Institute for Complex Molecular Systems, Eindhoven University of Technology, Eindhoven, the Netherlands; Department of Structural Biology and Biophysics, UCB Biopharma UK, Slough, UK.
  2. Seppe Leysen: Department of Structural Biology and Biophysics, UCB Biopharma UK, Slough, UK.
  3. Jeremy Davis: Department of Chemistry, UCB Biopharma UK, Slough, UK. Electronic address: Jeremy.Davis@ucb.com.
  4. Christian Ottmann: Laboratory of Chemical Biology, Department of Biomedical Engineering and Institute for Complex Molecular Systems, Eindhoven University of Technology, Eindhoven, the Netherlands. Electronic address: c.ottmann@tue.nl.

Abstract

Targeting protein-protein interactions (PPIs) has become a common approach to tackle various diseases whose pathobiology is driven by their mis-regulation in important signalling pathways. Modulating PPIs has tremendous untapped therapeutic potential and different approaches can be used to modulate PPIs. Initially, therapeutic effects were mostly sought by inhibiting PPIs. However, by gaining insight in the mode of action of certain therapeutic compounds, it became clear that stabilising (i.e. enhancing) PPIs can also be useful. The latter strategy is recently gaining a lot of attention, as stabilising physiologic, or even inducing novel interactions of a target protein with E3 ubiquitin ligases forms the basis of the targeted protein degradation (TPD) approach. An emerging additional example for drug discovery based on PPI stabilisation are the 14-3-3 proteins, a family of regulatory proteins, which engages in many protein-protein interactions, some of which might become therapeutical targets.

MeSH Term

Drug Discovery
Protein Interaction Mapping
Proteins
Signal Transduction

Chemicals

Proteins

Word Cloud

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