Aberrant Topologies of Bacterial Membrane Proteins Revealed by High Sensitivity Fluorescence Labelling

J Mol Biol. 2024 Jan 15;436(2):168368. doi: 10.1016/j.jmb.2023.168368. Epub 2023 Nov 15.

Abstract

The cytoplasmic membrane compartmentalises the bacterial cell into cytoplasm and periplasm. Proteins located in this membrane have a defined topology that is established during their biogenesis. However, the accuracy of this fundamental biosynthetic process is unknown. We developed compartment-specific fluorescence labelling methods with up to single-molecule sensitivity. Application of these methods to the single and multi-spanning membrane proteins of the Tat protein transport system revealed rare topogenesis errors. This methodology also detected low level soluble protein mislocalization from the cytoplasm to the periplasm. This study shows that it is possible to uncover rare errors in protein localization by leveraging the high sensitivity of fluorescence methods.

Keywords: Escherichia coli; Tat protein transport; fluorescence; membrane protein topology; periplasm.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Escherichia coli Proteins* / analysis
  • Escherichia coli* / chemistry
  • Escherichia coli* / metabolism
  • Fluorescence
  • Membrane Transport Proteins* / analysis
  • Membrane Transport Proteins* / metabolism
  • Periplasm / chemistry
  • Protein Transport
  • Single Molecule Imaging* / methods

Substances

  • Escherichia coli Proteins
  • Membrane Transport Proteins
  • twin-arginine translocase complex, E coli