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Structural basis for ?-opioid receptor binding and activation.


ABSTRACT: Opioids that stimulate the ?-opioid receptor (MOR1) are the most frequently prescribed and effective analgesics. Here we present a structural model of MOR1. Molecular dynamics simulations show a ligand-dependent increase in the conformational flexibility of the third intracellular loop that couples with the G protein complex. These simulations likewise identified residues that form frequent contacts with ligands. We validated the binding residues using site-directed mutagenesis coupled with radioligand binding and functional assays. The model was used to blindly screen a library of ?1.2 million compounds. From the 34 compounds predicted to be strong binders, the top three candidates were examined using biochemical assays. One compound showed high efficacy and potency. Post hoc testing revealed this compound to be nalmefene, a potent clinically used antagonist, thus further validating the model. In summary, the MOR1 model provides a tool for elucidating the structural mechanism of ligand-initiated cell signaling and for screening novel analgesics.

SUBMITTER: Serohijos AW 

PROVIDER: S-EPMC3217204 | biostudies-literature | 2011 Nov

REPOSITORIES: biostudies-literature

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Structural basis for μ-opioid receptor binding and activation.

Serohijos Adrian W R AW   Yin Shuangye S   Ding Feng F   Gauthier Josee J   Gibson Dustin G DG   Maixner William W   Dokholyan Nikolay V NV   Diatchenko Luda L  

Structure (London, England : 1993) 20111101 11


Opioids that stimulate the μ-opioid receptor (MOR1) are the most frequently prescribed and effective analgesics. Here we present a structural model of MOR1. Molecular dynamics simulations show a ligand-dependent increase in the conformational flexibility of the third intracellular loop that couples with the G protein complex. These simulations likewise identified residues that form frequent contacts with ligands. We validated the binding residues using site-directed mutagenesis coupled with radi  ...[more]

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