Fibulin-5 interacts with fibrillin-1 molecules and microfibrils

Biochem J. 2005 May 15;388(Pt 1):1-5. doi: 10.1042/BJ20050368.

Abstract

Fibulin-5 plays an important role in elastic fibre formation in vivo. We have investigated the molecular interactions between fibulin-5 and components of fibrillin-rich microfibrils which form a template for elastin. Fibulin-5 interacted in a dose-dependent manner with a fibrillin-1 N-terminal sequence and with tropoelastin, but not with MAGP-1 (microfibril-associated glycoprotein-1) or decorin. Fibulin-5 did not inhibit interactions between fibrillin-1 N- and C-terminal fragments, or fibrillin-1 interactions with tropoelastin. Fibulin-5 may provide a link between tropoelastin and microfibrils in the pericellular space during elastic fibre assembly.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Contractile Proteins / chemistry
  • Decorin
  • Extracellular Matrix Proteins / chemistry*
  • Fibrillin-1
  • Fibrillins
  • Humans
  • Microfibrils / chemistry*
  • Microfilament Proteins / chemistry*
  • Protein Binding
  • Protein Structure, Tertiary
  • Proteoglycans / chemistry
  • RNA Splicing Factors

Substances

  • Contractile Proteins
  • DCN protein, human
  • Decorin
  • Extracellular Matrix Proteins
  • FBLN5 protein, human
  • FBN1 protein, human
  • Fibrillin-1
  • Fibrillins
  • Microfilament Proteins
  • Proteoglycans
  • RNA Splicing Factors
  • microfibrillar protein