The conserved third transmembrane segment of YidC contacts nascent Escherichia coli inner membrane proteins

J Biol Chem. 2008 Dec 12;283(50):34635-42. doi: 10.1074/jbc.M804344200. Epub 2008 Oct 6.

Abstract

Escherichia coli YidC is a polytopic inner membrane protein that plays an essential and versatile role in the biogenesis of inner membrane proteins. YidC functions in Sec-dependent membrane insertion but acts also independently as a separate insertase for certain small membrane proteins. We have used a site-specific cross-linking approach to show that the conserved third transmembrane segment of YidC contacts the transmembrane domains of both nascent Sec-dependent and -independent substrates, indicating a generic recognition of insertion intermediates by YidC. Our data suggest that specific residues of the third YidC transmembrane segment alpha-helix is oriented toward the transmembrane domains of nascent inner membrane proteins that, in contrast, appear quite flexibly positioned at this stage in biogenesis.

MeSH terms

  • Amino Acid Sequence
  • Cell Membrane / metabolism*
  • Cross-Linking Reagents / chemistry
  • Cysteine / chemistry
  • Escherichia coli / metabolism*
  • Escherichia coli Proteins / metabolism*
  • Lipids / chemistry
  • Membrane Proteins / chemistry
  • Membrane Proteins / metabolism
  • Membrane Transport Proteins / metabolism*
  • Molecular Sequence Data
  • Mutation
  • Plasmids / metabolism
  • Protein Binding
  • Protein Conformation
  • Protein Structure, Secondary
  • Protein Structure, Tertiary

Substances

  • Cross-Linking Reagents
  • Escherichia coli Proteins
  • Lipids
  • Membrane Proteins
  • Membrane Transport Proteins
  • YIDC protein, E coli
  • Cysteine