An adjacent arginine, and the phosphorylated tyrosine in the c-Met receptor target sequence, dictates the orientation of c-Cbl binding

FEBS Lett. 2011 Jan 21;585(2):281-5. doi: 10.1016/j.febslet.2010.11.060. Epub 2010 Dec 15.

Abstract

Previously, we have demonstrated that the tyrosine phosphorylated hepatocyte growth factor receptor (Met) binds to the c-Cbl phosphotyrosine-recognition, tyrosine kinase binding (TKB) domain in a reverse orientation compared to other c-Cbl binding partners. A Met peptide with the DpYR motif changed to RpYD (MetRD) retains a similar TKB binding affinity as the native Met peptide. However, the TKB: MetRD complex crystal structure reveals a complete reversal of the binding orientation. Collated data indicates that both binding and orientation is dictated by the phosphorylated tyrosine and an adjacent arginine forming intra-peptide hydrogen bonds and aligning unidirectionally with complementary charges in the phosphotyrosine binding pocket of c-Cbl.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Motifs
  • Amino Acid Sequence
  • Arginine*
  • Crystallography, X-Ray
  • Humans
  • Hydrogen Bonding
  • Kinetics
  • Mass Spectrometry
  • Phosphotyrosine*
  • Protein Binding
  • Proto-Oncogene Proteins c-cbl / metabolism*
  • Proto-Oncogene Proteins c-met / chemistry
  • Proto-Oncogene Proteins c-met / metabolism*
  • Receptors, Growth Factor / chemistry
  • Receptors, Growth Factor / metabolism*
  • Surface Plasmon Resonance

Substances

  • Receptors, Growth Factor
  • Phosphotyrosine
  • Arginine
  • Proto-Oncogene Proteins c-cbl
  • MET protein, human
  • Proto-Oncogene Proteins c-met