Identification of a heparin binding domain of the neural cell adhesion molecule N-CAM using synthetic peptides

Neuron. 1989 Feb;2(2):1157-65. doi: 10.1016/0896-6273(89)90182-7.

Abstract

The neural cell adhesion molecule (N-CAM) plays an integral role in cell interactions during neural development, with the binding of heparan sulfate proteoglycan to the amino-terminal region of N-CAM being required for N-CAM function. In the present study we have used synthetic peptides (HBD-1 and HBD-2), derived from the primary amino acid sequence of rat N-CAM, to identify the region of N-CAM that binds heparan sulfate. The 28 amino acid HBD-1 synthetic peptide was shown to bind both [3H]heparin and dissociated retinal cells. Retinal cells also attach to a substratum of HBD-2 peptide, but fail to bind to a control peptide containing a scrambled amino acid sequence of HBD-2. The HBD-2 peptide also inhibits retinal cell adhesion to N-CAM, demonstrating the physiological importance of the amino acid sequence encoded by the HBD peptide. These data therefore permit the localization of a heparin binding domain to a 17 amino acid region of immunoglobulin-like loop 2.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Binding Sites
  • Cell Adhesion
  • Cell Adhesion Molecules, Neuronal / genetics
  • Cell Adhesion Molecules, Neuronal / metabolism*
  • Chick Embryo
  • DNA / genetics
  • Heparin / metabolism*
  • Heparitin Sulfate / metabolism
  • In Vitro Techniques
  • Kinetics
  • Molecular Sequence Data
  • Peptides / chemical synthesis*
  • Retina / cytology
  • Retina / physiology

Substances

  • Cell Adhesion Molecules, Neuronal
  • Peptides
  • Heparin
  • DNA
  • Heparitin Sulfate