Biosynthesis of the epidermal growth factor receptor: post-translational glycosylation-independent acquisition of tyrosine kinase autophosphorylation activity

Biochem Biophys Res Commun. 1988 May 31;153(1):96-103. doi: 10.1016/s0006-291x(88)81194-x.

Abstract

We previously showed that the epidermal growth factor (EGF) receptor in human A431 epidermoid carcinoma cells undergoes a slow post-translational modification whereby it acquires (t1/2 = 30-40 min) EGF binding capacity (Slieker, L.J., et. al. (1986) J. Biol. Chem., 261, 15233-15241). This activation occurs in the endoplasmic reticulum and requires core N-linked glycosylation. By employing both anti-EGF receptor and anti-phosphotyrosine antibodies to immunoprecipitate receptor pulse-labeled with [35S]methionine, we demonstrate here that the EGF receptor also acquires tyrosine kinase autophosphorylation activity post-translationally (t1/2 = 10-15 min). The acquisition of tyrosine kinase activity is independent of the acquisition of EGF binding capacity, since it precedes the latter process and does not require N-linked glycosylation.

Publication types

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

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Antibodies
  • Cell Line
  • Electrophoresis, Polyacrylamide Gel
  • ErbB Receptors / biosynthesis*
  • ErbB Receptors / genetics
  • Glycosylation
  • Humans
  • Molecular Weight
  • Phosphorylation
  • Phosphotyrosine
  • Protein Processing, Post-Translational*
  • Protein-Tyrosine Kinases / metabolism*
  • Tunicamycin / pharmacology
  • Tyrosine / analogs & derivatives
  • Tyrosine / analysis

Substances

  • Antibodies
  • Tunicamycin
  • Phosphotyrosine
  • Tyrosine
  • Adenosine Triphosphate
  • ErbB Receptors
  • Protein-Tyrosine Kinases