Ligand based conformational space studies of the μ-opioid receptor

Biochim Biophys Acta Gen Subj. 2021 Mar;1865(3):129838. doi: 10.1016/j.bbagen.2020.129838. Epub 2020 Dec 26.

Abstract

Background: G protein-coupled receptors (GPCRs) comprise a family of membrane proteins that can be activated by a variety of external factors. The μ-opioid receptor (MOR), a class A GPCR, is the main target of morphine. Recently, enhanced sampling molecular dynamics simulations of a constitutively active mutant of MOR in its apo form allowed us to capture the novel intermediate states of activation, as well as the active state. This prompted us to apply the same techniques to wild type MOR in complex with ligands, in order to explore their contributions to the receptor conformational changes in the activation process.

Methods: MOR was modeled in complex with agonists (morphine, BU72), a partial agonist (naloxone benzoylhydrazone) and an antagonist (naloxone). Replica exchange with solute tempering (REST2) molecular dynamics simulations were carried out for all systems. Trajectory frames were clustered, and the activation state of each cluster was assessed by two different methods.

Results: Cluster sizes and activation indices show that while agonists stabilized structures in a higher activation state, the antagonist behaved oppositely. Morphine tends to drive the receptor towards increasing R165-T279 distances, while naloxone tends to increase the NPxxYA motif conformational change.

Conclusions: Despite not observing a full transition between inactive and active states, an important conformational change of transmembrane helix 5 was observed and associated with a ligand-driven step of the process.

General significance: The activation process of GPCRs is widely studied but still not fully understood. Here we carried out a step forward in the direction of gaining more details of this process.

Keywords: GPCR; Molecular dynamics; PCA; μ-Opioid receptor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acids / chemistry*
  • Amino Acids / metabolism
  • Apoproteins / chemistry*
  • Apoproteins / metabolism
  • Binding Sites
  • Humans
  • Ligands
  • Lipid Bilayers / chemistry
  • Lipid Bilayers / metabolism
  • Molecular Docking Simulation
  • Molecular Dynamics Simulation
  • Morphinans / chemistry
  • Morphinans / metabolism
  • Morphine / chemistry*
  • Morphine / metabolism
  • Naloxone / analogs & derivatives
  • Naloxone / chemistry
  • Naloxone / metabolism
  • Phosphatidylcholines / chemistry*
  • Phosphatidylcholines / metabolism
  • Protein Binding
  • Protein Conformation, alpha-Helical
  • Pyrroles / chemistry
  • Pyrroles / metabolism
  • Receptors, Opioid, mu / chemistry*
  • Receptors, Opioid, mu / metabolism
  • Solutions
  • Water / chemistry
  • Water / metabolism

Substances

  • Amino Acids
  • Apoproteins
  • BU72 compound
  • Ligands
  • Lipid Bilayers
  • Morphinans
  • Phosphatidylcholines
  • Pyrroles
  • Receptors, Opioid, mu
  • Solutions
  • Water
  • naloxone benzoylhydrazone
  • Naloxone
  • Morphine
  • 1-palmitoyl-2-oleoylphosphatidylcholine