1. Academic Validation
  2. Energetics of lipid transport by the ABC transporter MsbA is lipid dependent

Energetics of lipid transport by the ABC transporter MsbA is lipid dependent

  • Commun Biol. 2021 Dec 9;4(1):1379. doi: 10.1038/s42003-021-02902-8.
Dawei Guo 1 Himansha Singh 1 Atsushi Shimoyama 2 Charlotte Guffick 1 Yakun Tang 1 Sam M Rowe 3 Timothy Noel 1 David R Spring 3 Koichi Fukase 2 Hendrik W van Veen 4
Affiliations

Affiliations

  • 1 Department of Pharmacology, University of Cambridge, Tennis Court Road, Cambridge, CB2 1PD, UK.
  • 2 Department of Chemistry, Osaka University, 1-1 Machikaneyama, Toyonaka, Osaka, 560-0043, Japan.
  • 3 Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge, CB2 1EW, UK.
  • 4 Department of Pharmacology, University of Cambridge, Tennis Court Road, Cambridge, CB2 1PD, UK. hwv20@cam.ac.uk.
Abstract

The ABC multidrug exporter MsbA mediates the translocation of lipopolysaccharides and Phospholipids across the plasma membrane in Gram-negative bacteria. Although MsbA is structurally well characterised, the energetic requirements of lipid transport remain unknown. Here, we report that, similar to the transport of small-molecule Antibiotics and cytotoxic agents, the flopping of physiologically relevant long-acyl-chain 1,2-dioleoyl (C18)-phosphatidylethanolamine in proteoliposomes requires the simultaneous input of ATP binding and hydrolysis and the chemical proton gradient as sources of metabolic energy. In contrast, the flopping of the large hexa-acylated (C12-C14) Lipid-A anchor of lipopolysaccharides is only ATP dependent. This study demonstrates that the energetics of lipid transport by MsbA is lipid dependent. As our mutational analyses indicate lipid and drug transport via the central binding chamber in MsbA, the lipid availability in the membrane can affect the drug transport activity and vice versa.

Figures
Products
  • Cat. No.
    Product Name
    Description
    Target
    Research Area
  • HY-125176
    98.14%, MsbA Antagonist