Binding specificities and affinities of egf domains for ErbB receptors

FEBS Lett. 1999 Mar 26;447(2-3):227-31. doi: 10.1016/s0014-5793(99)00283-5.

Abstract

ErbB receptor activation is a complex process and is dependent upon the type and number of receptors expressed on a given cell. Previous studies with defined combinations of ErbB receptors expressed in mammalian cells have helped elucidate specific biological responses for many of the recognized gene products that serve as ligands for these receptors. However, no study has examined the binding of these ligands in a defined experimental system. To address this issue, the relative binding affinities of the egf domains of eleven ErbB ligands were measured on six ErbB receptor combinations using a soluble receptor-ligand binding format. The ErbB2/4 heterodimer was shown to bind all ligands tested with moderate to very high affinity. In contrast, ErbB3 showed much more restrictive ligand binding specificity and measurable binding was observed only with heregulin, neuregulin2beta, epiregulin and the synthetic heregulin/egf chimera, biregulin. These studies also revealed that ErbB2 preferentially enhances ligand binding to ErbB3 or ErbB4 and to a lesser degree to ErbB1.

MeSH terms

  • Amino Acid Sequence
  • Betacellulin
  • Binding Sites
  • Carrier Proteins / chemistry
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism
  • Dimerization
  • Epidermal Growth Factor / chemistry
  • Epidermal Growth Factor / genetics
  • Epidermal Growth Factor / metabolism*
  • ErbB Receptors / chemistry
  • ErbB Receptors / metabolism*
  • Glycoproteins / chemistry
  • Glycoproteins / genetics
  • Glycoproteins / metabolism
  • Growth Substances / chemistry
  • Growth Substances / genetics
  • Growth Substances / metabolism
  • Heparin-binding EGF-like Growth Factor
  • Humans
  • In Vitro Techniques
  • Intercellular Signaling Peptides and Proteins*
  • Intracellular Signaling Peptides and Proteins*
  • Ligands
  • Macromolecular Substances
  • Molecular Sequence Data
  • Nerve Growth Factors / chemistry
  • Nerve Growth Factors / genetics
  • Nerve Growth Factors / metabolism
  • Neuregulins
  • Oncogene Proteins v-erbB / chemistry
  • Oncogene Proteins v-erbB / metabolism*
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / metabolism
  • Transforming Growth Factor alpha / chemistry
  • Transforming Growth Factor alpha / genetics
  • Transforming Growth Factor alpha / metabolism

Substances

  • BTC protein, human
  • Betacellulin
  • Btc protein, mouse
  • Carrier Proteins
  • Glycoproteins
  • Growth Substances
  • HBEGF protein, human
  • Hbegf protein, mouse
  • Heparin-binding EGF-like Growth Factor
  • Intercellular Signaling Peptides and Proteins
  • Intracellular Signaling Peptides and Proteins
  • Ligands
  • Macromolecular Substances
  • NRG2 protein, human
  • NRG3 protein, human
  • Nerve Growth Factors
  • Neuregulins
  • Nrg2 protein, mouse
  • Oncogene Proteins v-erbB
  • Recombinant Proteins
  • Transforming Growth Factor alpha
  • biregulin
  • Epidermal Growth Factor
  • ErbB Receptors