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Designing Selective Drug-like Molecular Glues for the Glucocorticoid Receptor/14-3-3 Protein–Protein Interaction

[Image: see text] The ubiquitously expressed glucocorticoid receptor (GR) is a nuclear receptor that controls a broad range of biological processes and is activated by steroidal glucocorticoids such as hydrocortisone or dexamethasone. Glucocorticoids are used to treat a wide variety of conditions, f...

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Autores principales: Pallesen, Jakob S., Munier, Claire C., Bosica, Francesco, Andrei, Sebastian A., Edman, Karl, Gunnarsson, Anders, La Sala, Giuseppina, Putra, Okky Dwichandra, Srdanović, Sonja, Wilson, Andrew J., Wissler, Lisa, Ottmann, Christian, Perry, Matthew W. D., O’Mahony, Gavin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9791658/
https://www.ncbi.nlm.nih.gov/pubmed/36484727
http://dx.doi.org/10.1021/acs.jmedchem.2c01635
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author Pallesen, Jakob S.
Munier, Claire C.
Bosica, Francesco
Andrei, Sebastian A.
Edman, Karl
Gunnarsson, Anders
La Sala, Giuseppina
Putra, Okky Dwichandra
Srdanović, Sonja
Wilson, Andrew J.
Wissler, Lisa
Ottmann, Christian
Perry, Matthew W. D.
O’Mahony, Gavin
author_facet Pallesen, Jakob S.
Munier, Claire C.
Bosica, Francesco
Andrei, Sebastian A.
Edman, Karl
Gunnarsson, Anders
La Sala, Giuseppina
Putra, Okky Dwichandra
Srdanović, Sonja
Wilson, Andrew J.
Wissler, Lisa
Ottmann, Christian
Perry, Matthew W. D.
O’Mahony, Gavin
author_sort Pallesen, Jakob S.
collection PubMed
description [Image: see text] The ubiquitously expressed glucocorticoid receptor (GR) is a nuclear receptor that controls a broad range of biological processes and is activated by steroidal glucocorticoids such as hydrocortisone or dexamethasone. Glucocorticoids are used to treat a wide variety of conditions, from inflammation to cancer but suffer from a range of side effects that motivate the search for safer GR modulators. GR is also regulated outside the steroid-binding site through protein–protein interactions (PPIs) with 14-3-3 adapter proteins. Manipulation of these PPIs will provide insights into noncanonical GR signaling as well as a new level of control over GR activity. We report the first molecular glues that selectively stabilize the 14-3-3/GR PPI using the related nuclear receptor estrogen receptor α (ERα) as a selectivity target to drive design. These 14-3-3/GR PPI stabilizers can be used to dissect noncanonical GR signaling and enable the development of novel atypical GR modulators.
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spelling pubmed-97916582022-12-27 Designing Selective Drug-like Molecular Glues for the Glucocorticoid Receptor/14-3-3 Protein–Protein Interaction Pallesen, Jakob S. Munier, Claire C. Bosica, Francesco Andrei, Sebastian A. Edman, Karl Gunnarsson, Anders La Sala, Giuseppina Putra, Okky Dwichandra Srdanović, Sonja Wilson, Andrew J. Wissler, Lisa Ottmann, Christian Perry, Matthew W. D. O’Mahony, Gavin J Med Chem [Image: see text] The ubiquitously expressed glucocorticoid receptor (GR) is a nuclear receptor that controls a broad range of biological processes and is activated by steroidal glucocorticoids such as hydrocortisone or dexamethasone. Glucocorticoids are used to treat a wide variety of conditions, from inflammation to cancer but suffer from a range of side effects that motivate the search for safer GR modulators. GR is also regulated outside the steroid-binding site through protein–protein interactions (PPIs) with 14-3-3 adapter proteins. Manipulation of these PPIs will provide insights into noncanonical GR signaling as well as a new level of control over GR activity. We report the first molecular glues that selectively stabilize the 14-3-3/GR PPI using the related nuclear receptor estrogen receptor α (ERα) as a selectivity target to drive design. These 14-3-3/GR PPI stabilizers can be used to dissect noncanonical GR signaling and enable the development of novel atypical GR modulators. American Chemical Society 2022-12-09 2022-12-22 /pmc/articles/PMC9791658/ /pubmed/36484727 http://dx.doi.org/10.1021/acs.jmedchem.2c01635 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Pallesen, Jakob S.
Munier, Claire C.
Bosica, Francesco
Andrei, Sebastian A.
Edman, Karl
Gunnarsson, Anders
La Sala, Giuseppina
Putra, Okky Dwichandra
Srdanović, Sonja
Wilson, Andrew J.
Wissler, Lisa
Ottmann, Christian
Perry, Matthew W. D.
O’Mahony, Gavin
Designing Selective Drug-like Molecular Glues for the Glucocorticoid Receptor/14-3-3 Protein–Protein Interaction
title Designing Selective Drug-like Molecular Glues for the Glucocorticoid Receptor/14-3-3 Protein–Protein Interaction
title_full Designing Selective Drug-like Molecular Glues for the Glucocorticoid Receptor/14-3-3 Protein–Protein Interaction
title_fullStr Designing Selective Drug-like Molecular Glues for the Glucocorticoid Receptor/14-3-3 Protein–Protein Interaction
title_full_unstemmed Designing Selective Drug-like Molecular Glues for the Glucocorticoid Receptor/14-3-3 Protein–Protein Interaction
title_short Designing Selective Drug-like Molecular Glues for the Glucocorticoid Receptor/14-3-3 Protein–Protein Interaction
title_sort designing selective drug-like molecular glues for the glucocorticoid receptor/14-3-3 protein–protein interaction
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9791658/
https://www.ncbi.nlm.nih.gov/pubmed/36484727
http://dx.doi.org/10.1021/acs.jmedchem.2c01635
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