In vivo cross-linking of the SecA and SecY subunits of the Escherichia coli preprotein translocase

J Bacteriol. 1997 Sep;179(18):5699-704. doi: 10.1128/jb.179.18.5699-5704.1997.

Abstract

Precursor protein translocation across the Escherichia coli inner membrane is mediated by the translocase, which is composed of a heterotrimeric integral membrane protein complex with SecY, SecE, and SecG as subunits and peripherally bound SecA. Cross-linking experiments were conducted to study which proteins are associated with SecA in vivo. Formaldehyde treatment of intact cells results in the specific cross-linking of SecA to SecY. Concurrently with the increased membrane association of SecA, an elevated amount of cross-linked product was obtained in cells harboring overproduced SecYEG complex. Cross-linked SecA copurified with hexahistidine-tagged SecY and not with SecE. The data indicate that SecA and SecY coexist as a stable complex in the cytoplasmic membrane in vivo.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphatases / chemistry*
  • Adenosine Triphosphatases / metabolism
  • Adenosine Triphosphate / metabolism
  • Bacterial Proteins / chemistry*
  • Bacterial Proteins / metabolism
  • Biological Transport
  • Cell Membrane / metabolism
  • Cross-Linking Reagents
  • Escherichia coli / chemistry
  • Escherichia coli / enzymology*
  • Escherichia coli / metabolism
  • Escherichia coli Proteins*
  • Membrane Transport Proteins*
  • Molecular Weight
  • Recombinant Proteins
  • SEC Translocation Channels
  • SecA Proteins

Substances

  • Bacterial Proteins
  • Cross-Linking Reagents
  • Escherichia coli Proteins
  • Membrane Transport Proteins
  • Recombinant Proteins
  • SEC Translocation Channels
  • SecY protein, E coli
  • Adenosine Triphosphate
  • Adenosine Triphosphatases
  • SecA Proteins