A pair of circularly permutated PDZ domains control RseP, the S2P family intramembrane protease of Escherichia coli

J Biol Chem. 2008 Dec 12;283(50):35042-52. doi: 10.1074/jbc.M806603200. Epub 2008 Oct 22.

Abstract

The sigma(E) pathway of extracytoplasmic stress responses in Escherichia coli is activated through sequential cleavages of the anti-sigma(E) protein, RseA, by membrane proteases DegS and RseP. Without the first cleavage by DegS, RseP is unable to cleave full-length RseA. We previously showed that a PDZ-like domain in the RseP periplasmic region is essential for this negative regulation of RseP. We now isolated additional deregulated RseP mutants. Many of the mutations affected a periplasmic region that is N-terminal to the previously defined PDZ domain. We expressed these regions and determined their crystal structures. Consistent with a recent prediction, our results indicate that RseP has tandem, circularly permutated PDZ domains (PDZ-N and PDZ-C). Strikingly, almost all the strong mutations have been mapped around the ligand binding cleft region in PDZ-N. These results together with those of an in vitro reaction reproducing the two-step RseA cleavage suggest that the proteolytic function of RseP is controlled by ligand binding to PDZ-N.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Crystallography, X-Ray / methods
  • Endopeptidases / chemistry*
  • Endopeptidases / metabolism
  • Escherichia coli / metabolism*
  • Escherichia coli Proteins / chemistry*
  • Escherichia coli Proteins / metabolism
  • Gene Expression Regulation*
  • Histidine / chemistry
  • Ligands
  • Membrane Proteins / chemistry*
  • Membrane Proteins / metabolism
  • Models, Genetic
  • Models, Molecular
  • Molecular Conformation
  • Mutation
  • Periplasm / metabolism
  • Plasmids / metabolism
  • Protein Conformation
  • Protein Structure, Tertiary
  • Time Factors

Substances

  • Escherichia coli Proteins
  • Ligands
  • Membrane Proteins
  • Histidine
  • Endopeptidases
  • RseP protein, E coli