Cargando…
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...
Autores principales: | , , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1784859458522841088 |
---|---|
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. |
format | Online Article Text |
id | pubmed-9791658 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT pallesenjakobs designingselectivedruglikemoleculargluesfortheglucocorticoidreceptor1433proteinproteininteraction AT munierclairec designingselectivedruglikemoleculargluesfortheglucocorticoidreceptor1433proteinproteininteraction AT bosicafrancesco designingselectivedruglikemoleculargluesfortheglucocorticoidreceptor1433proteinproteininteraction AT andreisebastiana designingselectivedruglikemoleculargluesfortheglucocorticoidreceptor1433proteinproteininteraction AT edmankarl designingselectivedruglikemoleculargluesfortheglucocorticoidreceptor1433proteinproteininteraction AT gunnarssonanders designingselectivedruglikemoleculargluesfortheglucocorticoidreceptor1433proteinproteininteraction AT lasalagiuseppina designingselectivedruglikemoleculargluesfortheglucocorticoidreceptor1433proteinproteininteraction AT putraokkydwichandra designingselectivedruglikemoleculargluesfortheglucocorticoidreceptor1433proteinproteininteraction AT srdanovicsonja designingselectivedruglikemoleculargluesfortheglucocorticoidreceptor1433proteinproteininteraction AT wilsonandrewj designingselectivedruglikemoleculargluesfortheglucocorticoidreceptor1433proteinproteininteraction AT wisslerlisa designingselectivedruglikemoleculargluesfortheglucocorticoidreceptor1433proteinproteininteraction AT ottmannchristian designingselectivedruglikemoleculargluesfortheglucocorticoidreceptor1433proteinproteininteraction AT perrymatthewwd designingselectivedruglikemoleculargluesfortheglucocorticoidreceptor1433proteinproteininteraction AT omahonygavin designingselectivedruglikemoleculargluesfortheglucocorticoidreceptor1433proteinproteininteraction |