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

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 interestin...

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Autores principales: Gigante, Alba, Sijbesma, Eline, Sánchez‐Murcia, Pedro A., Hu, Xiaoyu, Bier, David, Bäcker, Sandra, Knauer, Shirley, Gago, Federico, Ottmann, Christian, Schmuck, Carsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7155037/
https://www.ncbi.nlm.nih.gov/pubmed/31814236
http://dx.doi.org/10.1002/anie.201914517
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author Gigante, Alba
Sijbesma, Eline
Sánchez‐Murcia, Pedro A.
Hu, Xiaoyu
Bier, David
Bäcker, Sandra
Knauer, Shirley
Gago, Federico
Ottmann, Christian
Schmuck, Carsten
author_facet Gigante, Alba
Sijbesma, Eline
Sánchez‐Murcia, Pedro A.
Hu, Xiaoyu
Bier, David
Bäcker, Sandra
Knauer, Shirley
Gago, Federico
Ottmann, Christian
Schmuck, Carsten
author_sort Gigante, Alba
collection PubMed
description 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.
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spelling pubmed-71550372020-04-15 A Supramolecular Stabilizer of the 14‐3‐3ζ/ERα Protein‐Protein Interaction with a Synergistic Mode of Action Gigante, Alba Sijbesma, Eline Sánchez‐Murcia, Pedro A. Hu, Xiaoyu Bier, David Bäcker, Sandra Knauer, Shirley Gago, Federico Ottmann, Christian Schmuck, Carsten Angew Chem Int Ed Engl Communications 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. John Wiley and Sons Inc. 2020-02-11 2020-03-23 /pmc/articles/PMC7155037/ /pubmed/31814236 http://dx.doi.org/10.1002/anie.201914517 Text en © 2019 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Communications
Gigante, Alba
Sijbesma, Eline
Sánchez‐Murcia, Pedro A.
Hu, Xiaoyu
Bier, David
Bäcker, Sandra
Knauer, Shirley
Gago, Federico
Ottmann, Christian
Schmuck, Carsten
A Supramolecular Stabilizer of the 14‐3‐3ζ/ERα Protein‐Protein Interaction with a Synergistic Mode of Action
title A Supramolecular Stabilizer of the 14‐3‐3ζ/ERα Protein‐Protein Interaction with a Synergistic Mode of Action
title_full A Supramolecular Stabilizer of the 14‐3‐3ζ/ERα Protein‐Protein Interaction with a Synergistic Mode of Action
title_fullStr A Supramolecular Stabilizer of the 14‐3‐3ζ/ERα Protein‐Protein Interaction with a Synergistic Mode of Action
title_full_unstemmed A Supramolecular Stabilizer of the 14‐3‐3ζ/ERα Protein‐Protein Interaction with a Synergistic Mode of Action
title_short A Supramolecular Stabilizer of the 14‐3‐3ζ/ERα Protein‐Protein Interaction with a Synergistic Mode of Action
title_sort supramolecular stabilizer of the 14‐3‐3ζ/erα protein‐protein interaction with a synergistic mode of action
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7155037/
https://www.ncbi.nlm.nih.gov/pubmed/31814236
http://dx.doi.org/10.1002/anie.201914517
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