tetano
Editor, Senior Moderator
Front Immunol
. 2022 Jun 15;13:906687.
doi: 10.3389/fimmu.2022.906687. eCollection 2022.
Glucocorticoids Bind to SARS-CoV-2 S1 at Multiple Sites Causing Cooperative Inhibition of SARS-CoV-2 S1 Interaction With ACE2
Hassan Sarker[SUP] 1 [/SUP], Rashmi Panigrahi[SUP] 1 [/SUP], Eugenio Hardy[SUP] 2 [/SUP], J N Mark Glover[SUP] 1 [/SUP], Shokrollah Elahi[SUP] 3 4 5 [/SUP], Carlos Fernandez-Patron[SUP] 1 [/SUP]
Affiliations
Abstract
Dexamethasone may reduce mortality in COVID-19 patients. Whether dexamethasone or endogenous glucocorticoids, such as cortisol, biochemically interact with SARS-CoV-2 spike 1 protein (S1), or its cellular receptor ACE2, is unknown. Using molecular dynamics (MD) simulations and binding energy calculations, we identified 162 druggable pockets in various conformational states of S1 and all possible binding pockets for cortisol and dexamethasone. Through biochemical binding studies, we confirmed that cortisol and dexamethasone bind to S1. Limited proteolysis and mass spectrometry analyses validated several MD identified binding pockets for cortisol and dexamethasone on S1. Interaction assays indicated that cortisol and dexamethasone separately and cooperatively disrupt S1 interaction with ACE2, through direct binding to S1, without affecting ACE2 catalytic activity. Cortisol disrupted the binding of the mutant S1 Beta variant (E484K, K417N, N501Y) to ACE2. Delta and Omicron variants are mutated in or near identified cortisol-binding pockets in S1, which may affect cortisol binding to them. In the presence of cortisol, we find increased inhibition of S1 binding to ACE2 by an anti-SARS-CoV-2 S1 human chimeric monoclonal antibody against the receptor binding domain. Whether glucocorticoid/S1 direct interaction is an innate defence mechanism that may have contributed to mild or asymptomatic SARS-CoV-2 infection deserves further investigation.
Keywords: ACE2 (angiotensin converting enzyme 2); COVID; SARS-CoV-2; coronavirus; glucocorticoids; innate immunity.
. 2022 Jun 15;13:906687.
doi: 10.3389/fimmu.2022.906687. eCollection 2022.
Glucocorticoids Bind to SARS-CoV-2 S1 at Multiple Sites Causing Cooperative Inhibition of SARS-CoV-2 S1 Interaction With ACE2
Hassan Sarker[SUP] 1 [/SUP], Rashmi Panigrahi[SUP] 1 [/SUP], Eugenio Hardy[SUP] 2 [/SUP], J N Mark Glover[SUP] 1 [/SUP], Shokrollah Elahi[SUP] 3 4 5 [/SUP], Carlos Fernandez-Patron[SUP] 1 [/SUP]
Affiliations
- PMID: 35784352
- PMCID: PMC9242398
- DOI: 10.3389/fimmu.2022.906687
Abstract
Dexamethasone may reduce mortality in COVID-19 patients. Whether dexamethasone or endogenous glucocorticoids, such as cortisol, biochemically interact with SARS-CoV-2 spike 1 protein (S1), or its cellular receptor ACE2, is unknown. Using molecular dynamics (MD) simulations and binding energy calculations, we identified 162 druggable pockets in various conformational states of S1 and all possible binding pockets for cortisol and dexamethasone. Through biochemical binding studies, we confirmed that cortisol and dexamethasone bind to S1. Limited proteolysis and mass spectrometry analyses validated several MD identified binding pockets for cortisol and dexamethasone on S1. Interaction assays indicated that cortisol and dexamethasone separately and cooperatively disrupt S1 interaction with ACE2, through direct binding to S1, without affecting ACE2 catalytic activity. Cortisol disrupted the binding of the mutant S1 Beta variant (E484K, K417N, N501Y) to ACE2. Delta and Omicron variants are mutated in or near identified cortisol-binding pockets in S1, which may affect cortisol binding to them. In the presence of cortisol, we find increased inhibition of S1 binding to ACE2 by an anti-SARS-CoV-2 S1 human chimeric monoclonal antibody against the receptor binding domain. Whether glucocorticoid/S1 direct interaction is an innate defence mechanism that may have contributed to mild or asymptomatic SARS-CoV-2 infection deserves further investigation.
Keywords: ACE2 (angiotensin converting enzyme 2); COVID; SARS-CoV-2; coronavirus; glucocorticoids; innate immunity.