An octameric PqiC toroid stabilises the outer-membrane interaction of the PqiABC transport system

EMBO Rep. 2024 Jan;25(1):82-101. doi: 10.1038/s44319-023-00014-4. Epub 2024 Jan 16.

Abstract

The E. coli Paraquat Inducible (Pqi) Pathway is a putative Gram-negative phospholipid transport system. The pathway comprises three components: an integral inner membrane protein (PqiA), a periplasmic spanning MCE family protein (PqiB) and an outer membrane lipoprotein (PqiC). Interactions between all complex components, including stoichiometry, remain uncharacterised; nevertheless, once assembled into their quaternary complex, the trio of Pqi proteins are anticipated to provide a continuous channel between the inner and outer membranes of diderms. Here, we present X-ray structures of both the native and a truncated, soluble construct of the PqiC lipoprotein, providing insight into its biological assembly, and utilise neutron reflectometry to characterise the nature of the PqiB-PqiC-membrane interaction. Finally, we employ phenotypic complementation assays to probe specific PqiC residues, which imply the interaction between PqiB and PqiC is less intimate than previously anticipated.

Keywords: Envelope Spanning; Gram Negative Cell Envelope; Lipid Transport; Outer Membrane Biogenesis; Pqi.

MeSH terms

  • Biological Transport
  • Escherichia coli Proteins* / chemistry
  • Escherichia coli* / genetics
  • Escherichia coli* / metabolism
  • Lipoproteins / metabolism
  • Membrane Proteins / metabolism

Substances

  • Escherichia coli Proteins
  • Membrane Proteins
  • Lipoproteins