Glucocorticoid resistance conferring mutation in the C-terminus of GR alters the receptor conformational dynamics

Abstract The glucocorticoid receptor is a key regulator of essential physiological processes, which under the control of the Hsp90 chaperone machinery, binds to steroid hormones and steroid-like molecules and in a rather complicated and elusive response, regulates a set of glucocorticoid responsive...

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Main Authors: Anna Kaziales, Florian Rührnößl, Klaus Richter
Format: Article
Language:English
Published: Nature Publishing Group 2021-06-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-92039-9
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spelling doaj-8c9e6a950a04427ab5b02f857827df8d2021-06-20T11:36:59ZengNature Publishing GroupScientific Reports2045-23222021-06-0111111410.1038/s41598-021-92039-9Glucocorticoid resistance conferring mutation in the C-terminus of GR alters the receptor conformational dynamicsAnna Kaziales0Florian Rührnößl1Klaus Richter2Department of Chemistry, Center for Integrated Protein Science Munich, Technische Universität MünchenDepartment of Chemistry, Center for Integrated Protein Science Munich, Technische Universität MünchenDepartment of Chemistry, Center for Integrated Protein Science Munich, Technische Universität MünchenAbstract The glucocorticoid receptor is a key regulator of essential physiological processes, which under the control of the Hsp90 chaperone machinery, binds to steroid hormones and steroid-like molecules and in a rather complicated and elusive response, regulates a set of glucocorticoid responsive genes. We here examine a human glucocorticoid receptor variant, harboring a point mutation in the last C-terminal residues, L773P, that was associated to Primary Generalized Glucocorticoid Resistance, a condition originating from decreased affinity to hormone, impairing one or multiple aspects of GR action. Using in vitro and in silico methods, we assign the conformational consequences of this mutation to particular GR elements and report on the altered receptor properties regarding its binding to dexamethasone, a NCOA-2 coactivator-derived peptide, DNA, and importantly, its interaction with the chaperone machinery of Hsp90.https://doi.org/10.1038/s41598-021-92039-9
collection DOAJ
language English
format Article
sources DOAJ
author Anna Kaziales
Florian Rührnößl
Klaus Richter
spellingShingle Anna Kaziales
Florian Rührnößl
Klaus Richter
Glucocorticoid resistance conferring mutation in the C-terminus of GR alters the receptor conformational dynamics
Scientific Reports
author_facet Anna Kaziales
Florian Rührnößl
Klaus Richter
author_sort Anna Kaziales
title Glucocorticoid resistance conferring mutation in the C-terminus of GR alters the receptor conformational dynamics
title_short Glucocorticoid resistance conferring mutation in the C-terminus of GR alters the receptor conformational dynamics
title_full Glucocorticoid resistance conferring mutation in the C-terminus of GR alters the receptor conformational dynamics
title_fullStr Glucocorticoid resistance conferring mutation in the C-terminus of GR alters the receptor conformational dynamics
title_full_unstemmed Glucocorticoid resistance conferring mutation in the C-terminus of GR alters the receptor conformational dynamics
title_sort glucocorticoid resistance conferring mutation in the c-terminus of gr alters the receptor conformational dynamics
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2021-06-01
description Abstract The glucocorticoid receptor is a key regulator of essential physiological processes, which under the control of the Hsp90 chaperone machinery, binds to steroid hormones and steroid-like molecules and in a rather complicated and elusive response, regulates a set of glucocorticoid responsive genes. We here examine a human glucocorticoid receptor variant, harboring a point mutation in the last C-terminal residues, L773P, that was associated to Primary Generalized Glucocorticoid Resistance, a condition originating from decreased affinity to hormone, impairing one or multiple aspects of GR action. Using in vitro and in silico methods, we assign the conformational consequences of this mutation to particular GR elements and report on the altered receptor properties regarding its binding to dexamethasone, a NCOA-2 coactivator-derived peptide, DNA, and importantly, its interaction with the chaperone machinery of Hsp90.
url https://doi.org/10.1038/s41598-021-92039-9
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AT klausrichter glucocorticoidresistanceconferringmutationinthecterminusofgraltersthereceptorconformationaldynamics
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