Beyond dimerization: a membrane-dependent activation model for interleukin-4 receptor-mediated signalling

J Mol Biol. 2007 Mar 9;366(5):1365-73. doi: 10.1016/j.jmb.2006.11.095. Epub 2006 Dec 6.

Abstract

Class I cytokine receptors efficiently transfer activation signals from the extracellular space to the cytoplasm and play a dominant role in growth control and differentiation of human tissues. Although a significant body of literature is devoted to this topic, a consistent mechanistic picture for receptor activation in the membrane environment is still missing. Using the interleukin-4 receptor (IL-4R) as an example, we propose that the membrane-proximal stem-loop of the extracellular domains contains pivotal elements of a rotational switch. Interfacial energies of amino acid side-chains contained in the highly conserved WSXWS at the surface of the lipid bilayer suggest a new functional role for this motif. A generic activation mechanism for this receptor class is presented, which may impact the design of a new generation of biophysical assay systems.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Amino Acid Motifs
  • Amino Acid Sequence
  • Cell Membrane / chemistry
  • Cell Membrane / metabolism
  • Conserved Sequence
  • Dimerization
  • Humans
  • Ligands
  • Lipid Bilayers / chemistry
  • Models, Molecular
  • Protein Structure, Secondary
  • Protein Structure, Tertiary
  • Receptors, Interleukin-4 / chemistry
  • Receptors, Interleukin-4 / metabolism*
  • Signal Transduction*

Substances

  • Ligands
  • Lipid Bilayers
  • Receptors, Interleukin-4