Saleh, N;
Saladino, G;
Gervasio, FL;
Haensele, E;
Banting, L;
Whitley, DC;
Sopkova-de Oliveira Santos, J;
... Clark, T; + view all
(2016)
A Three-Site Mechanism for Agonist/Antagonist Selective Binding to Vasopressin Receptors.
Angewandte Chemie International Edition
, 55
(28)
pp. 8008-8012.
10.1002/anie.201602729.
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Abstract
Molecular-dynamics simulations with metadynamics enhanced sampling reveal three distinct binding sites for arginine vasopressin (AVP) within its V2 -receptor (V2 R). Two of these, the vestibule and intermediate sites, block (antagonize) the receptor, and the third is the orthosteric activation (agonist) site. The contacts found for the orthosteric site satisfy all the requirements deduced from mutagenesis experiments. Metadynamics simulations for V2 R and its V1a R-analog give an excellent correlation with experimental binding free energies by assuming that the most stable binding site in the simulations corresponds to the experimental binding free energy in each case. The resulting three-site mechanism separates agonists from antagonists and explains subtype selectivity.
Type: | Article |
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Title: | A Three-Site Mechanism for Agonist/Antagonist Selective Binding to Vasopressin Receptors |
Open access status: | An open access version is available from UCL Discovery |
DOI: | 10.1002/anie.201602729 |
Publisher version: | http://dx.doi.org/10.1002/anie.201602729 |
Language: | English |
Additional information: | © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. This is the peer reviewed version of the following article: Saleh, N; Saladino, G; Gervasio, FL; Haensele, E; Banting, L; Whitley, DC; Sopkova-de Oliveira Santos, J; (2016) A Three-Site Mechanism for Agonist/Antagonist Selective Binding to Vasopressin Receptors. Angewandte Chemie International Edition, which has been published in final form at: http://dx.doi.org/10.1002/anie.201602729. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving. |
Keywords: | G-protein coupled receptors, hormones, metadynamics, molecular dynamics, receptors |
UCL classification: | UCL UCL > Provost and Vice Provost Offices > UCL BEAMS UCL > Provost and Vice Provost Offices > UCL BEAMS > Faculty of Maths and Physical Sciences UCL > Provost and Vice Provost Offices > UCL BEAMS > Faculty of Maths and Physical Sciences > Dept of Chemistry |
URI: | https://discovery.ucl.ac.uk/id/eprint/1493781 |
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