Structural and Functional Effect of an Oscillating Electric Field on the Dopamine-D3 Receptor: A Molecular Dynamics Simulation Study

PLoS One. 2016 Nov 10;11(11):e0166412. doi: 10.1371/journal.pone.0166412. eCollection 2016.

Abstract

Dopamine as a neurotransmitter plays a critical role in the functioning of the central nervous system. The structure of D3 receptor as a member of class A G-protein coupled receptors (GPCRs) has been reported. We used MD simulation to investigate the effect of an oscillating electric field, with frequencies in the range 0.6-800 GHz applied along the z-direction, on the dopamine-D3R complex. The simulations showed that at some frequencies, the application of an external oscillating electric field along the z-direction has a considerable effect on the dopamine-D3R. However, there is no enough evidence for prediction of changes in specific frequency, implying that there is no order in changes. Computing the correlation coefficient parameter showed that increasing the field frequency can weaken the interaction between dopamine and D3R and may decrease the Arg128{3.50}-Glu324{6.30} distance. Because of high stability of α helices along the z-direction, applying an oscillating electric field in this direction with an amplitude 10-time higher did not have a considerable effect. However, applying the oscillating field at the frequency of 0.6 GHz along other directions, such as X-Y and Y-Z planes, could change the energy between the dopamine and the D3R, and the number of internal hydrogen bonds of the protein. This can be due to the effect of the direction of the electric field vis-à-vis the ligands orientation and the interaction of the oscillating electric field with the dipole moment of the protein.

MeSH terms

  • Crystallography, X-Ray
  • Dopamine / metabolism*
  • Electricity
  • Humans
  • Lipid Bilayers / metabolism
  • Molecular Dynamics Simulation
  • Phosphatidylcholines / metabolism
  • Protein Binding
  • Protein Conformation
  • Receptors, Dopamine D3 / chemistry
  • Receptors, Dopamine D3 / metabolism*

Substances

  • Lipid Bilayers
  • Phosphatidylcholines
  • Receptors, Dopamine D3
  • 1-palmitoyl-2-oleoylphosphatidylcholine
  • Dopamine

Grants and funding

The authors received no specific funding for this work.