Download MendeleyMolecular control of delta-opioid receptor signalling.
Fenalti, G., Giguere, P.M., Katritch, V., Huang, X.P., Thompson, A.A., Cherezov, V., Roth, B.L., Stevens, R.C.(2014) Nature 506: 191-196
- PubMed: 24413399
- DOI: https://doi.org/10.1038/nature12944
- Primary Citation of Related Structures:
4N6H - PubMed Abstract:
Opioids represent widely prescribed and abused medications, although their signal transduction mechanisms are not well understood. Here we present the 1.8?? high-resolution crystal structure of the human ¦Ä-opioid receptor (¦Ä-OR), revealing the presence and fundamental role of a sodium ion in mediating allosteric control of receptor functional selectivity and constitutive activity. The distinctive ¦Ä-OR sodium ion site architecture is centrally located in a polar interaction network in the seven-transmembrane bundle core, with the sodium ion stabilizing a reduced agonist affinity state, and thereby modulating signal transduction. Site-directed mutagenesis and functional studies reveal that changing the allosteric sodium site residue Asn?131 to an alanine or a valine augments constitutive ¦Â-arrestin-mediated signalling. Asp95Ala, Asn310Ala and Asn314Ala mutations transform classical ¦Ä-opioid antagonists such as naltrindole into potent ¦Â-arrestin-biased agonists. The data establish the molecular basis for allosteric sodium ion control in opioid signalling, revealing that sodium-coordinating residues act as 'efficacy switches' at a prototypic G-protein-coupled receptor.
Organizational Affiliation:
1] Department of Integrative Structural and Computational Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, USA [2].
