Structural requirements of the extracellular to transmembrane domain junction for erythropoietin receptor function

J Biol Chem. 2005 Apr 15;280(15):14844-54. doi: 10.1074/jbc.M411251200. Epub 2005 Jan 18.

Abstract

The erythropoietin receptor (EpoR) is crucial for erythrocyte formation. The x-ray crystal structures of the EpoR extracellular domain lack the juxtamembrane (JM) region and the junction to the transmembrane (TM) domain. Yet the JM-TM regions are important for transmitting the conformational change imposed on the receptor dimer by Epo binding. Cysteine-scanning mutagenesis of the JM-TM regions identified three novel constitutively active mutants, demonstrating close disulfide-bonded juxtapositioning of these residues in the JM (L223C) and N-terminal TM domain (L226C, I227C). Chemical cross-linking defined the interface of the active helical TM dimer and revealed that the JM-TM segment encompassing Leu(226)-Leu(230) is non-helical. Molecular dynamics and NMR studies indicated that the TM-JM junction forms an N-terminal helix cap. This structure is important for EpoR function because replacement of this motif by consecutive leucines rendered the receptor constitutively active.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Motifs
  • Animals
  • Blotting, Western
  • Cell Line
  • Cell Membrane / metabolism
  • Cell Proliferation
  • Cell Separation
  • Cross-Linking Reagents / pharmacology
  • Crystallography, X-Ray
  • Cysteine / chemistry
  • DNA Mutational Analysis
  • DNA, Complementary / metabolism
  • Dimerization
  • Disulfides / chemistry
  • Flow Cytometry
  • Glycine / analogs & derivatives*
  • Glycine / chemistry
  • Growth Substances / metabolism
  • Humans
  • Leucine / chemistry
  • Luciferases / metabolism
  • Magnetic Resonance Spectroscopy
  • Mice
  • Mutagenesis
  • Mutagenesis, Site-Directed
  • Mutation
  • Peptides / chemistry
  • Phosphorylation
  • Protein Binding
  • Protein Conformation
  • Protein Structure, Secondary
  • Protein Structure, Tertiary
  • Receptors, Erythropoietin / chemistry*
  • Receptors, Erythropoietin / metabolism
  • Transfection

Substances

  • Cross-Linking Reagents
  • DNA, Complementary
  • Disulfides
  • Growth Substances
  • Peptides
  • Receptors, Erythropoietin
  • Luciferases
  • Leucine
  • Cysteine
  • Glycine
  • tricine