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Collagen and fibronectin (FN) are two abundant and essential components of the vertebrate extracellular matrix; they interact directly with cellular receptors and affect cell adhesion and migration. Past studies identified a FN fragment comprising six modules, (6)FnI(1-2)FnII(7-9)FnI, and termed the gelatin binding domain (GBD) as responsible for collagen interaction. Recently, we showed that the GBD binds tightly to a specific site within type I collagen and determined the structure of domains (8-9)FnI in complex with a peptide from that site. Here, we present the crystallographic structure of domains (6)FnI(1-2)FnII(7)FnI, which form a compact, globular unit through interdomain interactions. Analysis of NMR titrations with single-stranded collagen peptides reveals a dominant collagen interaction surface on domains (2)FnII and (7)FnI; a similar surface appears involved in interactions with triple-helical peptides. Models of the complete GBD, based on the new structure and the (8-9)FnI·collagen complex show a continuous putative collagen binding surface. We explore the implications of this model using long collagen peptides and discuss our findings in the context of FN interactions with collagen fibrils.

Original publication

DOI

10.1074/jbc.M110.139394

Type

Journal article

Journal

J Biol Chem

Publication Date

29/10/2010

Volume

285

Pages

33764 - 33770

Keywords

Animals, Binding Sites, Cell Movement, Circular Dichroism, Collagen, Crystallography, X-Ray, Fibronectins, Magnetic Resonance Spectroscopy, Peptides, Pichia, Protein Binding, Protein Conformation, Recombinant Proteins, Solvents