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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2021-06-01
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Online Access: | https://doi.org/10.1038/s41598-021-92039-9 |
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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 |
work_keys_str_mv |
AT annakaziales glucocorticoidresistanceconferringmutationinthecterminusofgraltersthereceptorconformationaldynamics AT florianruhrnoßl glucocorticoidresistanceconferringmutationinthecterminusofgraltersthereceptorconformationaldynamics AT klausrichter glucocorticoidresistanceconferringmutationinthecterminusofgraltersthereceptorconformationaldynamics |
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1721369888663011328 |