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A Supramolecular Stabilizer of the 14-3-3ζ/ERα Protein-Protein Interaction with a Synergistic Mode of Action.

Alba GiganteEline SijbesmaPedro A Sánchez-MurciaXiaoyu HuDavid BierSandra BäckerShirley KnauerFederico GagoChristian OttmannCarsten Schmuck
Published in: Angewandte Chemie (International ed. in English) (2020)
We report on a stabilizer of the interaction between 14-3-3ζ and the Estrogen Receptor alpha (ERα). ERα is a driver in the majority of breast cancers and 14-3-3 proteins are negative regulators of this nuclear receptor, making the stabilization of this protein-protein interaction (PPI) an interesting strategy. The stabilizer (1) consists of three symmetric peptidic arms containing an arginine mimetic, previously described as the GCP motif. 1 stabilizes the 14-3-3ζ/ERα interaction synergistically with the natural product Fusicoccin-A and was thus hypothesized to bind to a different site. This is supported by computational analysis of 1 binding to the binary complex of 14-3-3 and an ERα-derived phosphopeptide. Furthermore, 1 shows selectivity towards 14-3-3ζ/ERα interaction over other 14-3-3 client-derived phosphomotifs. These data provide a solid support of a new binding mode for a supramolecular 14-3-3ζ/ERα PPI stabilizer.
Keyphrases
  • data analysis
  • estrogen receptor
  • protein protein
  • endoplasmic reticulum
  • small molecule
  • breast cancer cells
  • nitric oxide
  • machine learning
  • water soluble
  • ionic liquid