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Fibronectin (FN) is a large extracellular matrix glycoprotein important for development and wound healing in vertebrates. Recent work has focused on the ability of FN fragments and embryonic or tumorigenic splicing variants to stimulate fibroblast migration into collagen gels. This activity has been localized to specific sites and is not exhibited by full-length FN. Here we show that an N-terminal FN fragment, spanning the migration stimulation sites and including the first three type III FN domains, also lacks this activity. A screen for interdomain interactions by solution-state NMR spectroscopy revealed specific contacts between the Fn N terminus and two of the type III domains. A single amino acid substitution, R222A, disrupts the strongest interaction, between domains (4-5)FnI and (3)FnIII, and restores motogenic activity to the FN N-terminal fragment. Anastellin, which promotes fibril formation, destabilizes (3)FnIII and disrupts the observed (4-5)FnI-(3)FnIII interaction. We discuss these findings in the context of the control of cellular activity through exposure of masked sites.

Original publication

DOI

10.1074/jbc.M109.003673

Type

Journal article

Journal

J Biol Chem

Publication Date

05/06/2009

Volume

284

Pages

15668 - 15675

Keywords

Alternative Splicing, Amino Acid Substitution, Animals, Cell Line, Chromatography, Gel, Collagen, Cytokines, Escherichia coli, Fibronectins, Genetic Variation, Humans, Kidney, Magnetic Resonance Spectroscopy, Models, Molecular, Peptide Fragments, Pichia, Protein Conformation, Rats, Recombinant Proteins, Tail, Tendons, Wound Healing