Characterizing Membrane Association and Periplasmic Transfer of Bacterial Lipoproteins through Molecular Dynamics Simulations

Structure. 2020 Apr 7;28(4):475-487.e3. doi: 10.1016/j.str.2020.01.012. Epub 2020 Feb 12.

Abstract

Escherichia coli lipoprotein precursors at the inner membrane undergo three maturation stages before transport by the Lol system to the outer membrane. Here, we develop a pipeline to simulate the membrane association of bacterial lipoproteins in their four maturation states. This has enabled us to model and simulate 81 of the predicted 114 E. coli lipoproteins and reveal their interactions with the host lipid membrane. As part of this set we characterize the membrane contacts of LolB, the lipoprotein involved in periplasmic translocation. We also consider the means and bioenergetics for lipoprotein localization. Our calculations uncover a preference for LolB over LolA and therefore indicate how a lipoprotein may be favorably transferred from the inner to outer membrane. Finally, we reveal that LolC has a role in membrane destabilization, thereby promoting lipoprotein transfer to LolA.

Keywords: antibiotics; biogenesis; lipoprotein; membrane proteins; molecular simulation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Outer Membrane / chemistry
  • Bacterial Outer Membrane / metabolism*
  • Bacterial Outer Membrane Proteins / chemistry*
  • Bacterial Outer Membrane Proteins / metabolism
  • Escherichia coli
  • Escherichia coli Proteins / chemistry*
  • Escherichia coli Proteins / metabolism
  • Molecular Chaperones / chemistry*
  • Molecular Chaperones / metabolism
  • Molecular Dynamics Simulation*
  • Periplasm / metabolism
  • Periplasmic Binding Proteins / chemistry*
  • Periplasmic Binding Proteins / metabolism
  • Protein Binding
  • Protein Transport

Substances

  • Bacterial Outer Membrane Proteins
  • Escherichia coli Proteins
  • LolA protein, E coli
  • LolB protein, E coli
  • Molecular Chaperones
  • Periplasmic Binding Proteins