In vitro analysis of the stop-transfer process during translocation across the cytoplasmic membrane of Escherichia coli

J Biol Chem. 1997 Aug 8;272(32):20082-7. doi: 10.1074/jbc.272.32.20082.

Abstract

In this study, using a derivative of proOmpA containing an artificial stop-transfer sequence (proOmpA2xH1), we analyzed the process of stop-transfer during translocation across the cytoplasmic membrane of Escherichia coli. ProOmpA2xH1 did not interfere with the transit of wild-type proOmpA. When proOmpA2xH1 was anchored in the membrane, membrane-inserted SecA was deinserted with the reversion of the inverted topology of SecG. Cross-linking experiments revealed that the anchored proOmpA2xH1 that does not interact with either SecY or SecA. These results, taken together, suggest that proOmpA2xH1 leaves the translocation pathway by means of a specific interaction between the stop-transfer sequence and the translocational channel.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Bacterial Outer Membrane Proteins / chemistry
  • Bacterial Outer Membrane Proteins / metabolism*
  • Bacterial Proteins / metabolism
  • Binding Sites
  • Biological Transport
  • Cytoplasm / metabolism
  • Escherichia coli / metabolism*
  • Escherichia coli Proteins*
  • Hydrolysis
  • Intracellular Membranes / metabolism
  • Membrane Proteins / metabolism
  • Protein Conformation
  • Protein Precursors / chemistry
  • Protein Precursors / metabolism*
  • SEC Translocation Channels

Substances

  • Bacterial Outer Membrane Proteins
  • Bacterial Proteins
  • Escherichia coli Proteins
  • Membrane Proteins
  • Protein Precursors
  • SEC Translocation Channels
  • SecG protein, E coli
  • outer membrane protein A precursor (E coli)
  • Adenosine Triphosphate