Isolation of an actin-binding fragment of fibronectin

Biochem J. 1981 Feb 1;193(2):615-20. doi: 10.1042/bj1930615.

Abstract

We have identified a specific actin-binding site in the adhesive glycoprotein fibronectin, isolated from chicken fibroblasts. Affinity chromatography of fragments, released from fibronectin by limited proteolysis with trypsin, chymotrypsin and subtilisin, on actin-Sepharose and other protein-Sepharose columns was used to locate the binding site. A 27 000-mol.wt. subtilisin-digest fragment bound efficiently to actin. The results suggest that the actin-binding site is close to, but not identical with, the reported collagen-binding site.

Publication types

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

MeSH terms

  • Actins / metabolism*
  • Animals
  • Binding Sites
  • Chickens
  • Chromatography, Affinity
  • Chymotrypsin / metabolism
  • Electrophoresis, Polyacrylamide Gel
  • Fibronectins / metabolism*
  • Gelatin / metabolism
  • Peptide Fragments / isolation & purification*
  • Protein Binding
  • Subtilisins / metabolism
  • Trypsin / metabolism

Substances

  • Actins
  • Fibronectins
  • Peptide Fragments
  • Gelatin
  • Subtilisins
  • Chymotrypsin
  • Trypsin