Architectures of Lipid Transport Systems for the Bacterial Outer Membrane

Damian C Ekiert1, Gira Bhabha2, Georgia L Isom3

  • 1Department of Cellular and Molecular Pharmacology and the Howard Hughes Medical Institute, The University of California, San Francisco, 600 16(th) Street, San Francisco, CA 94158, USA; Department of Microbiology and Immunology, The University of California, San Francisco, 600 16(th) Street, San Francisco, CA 94158, USA.

Cell
|April 8, 2017
PubMed

Insights

Researchers discovered how phospholipids move between bacterial membranes using protein channels. The mammalian cell entry (MCE) protein family forms diverse structures, including rings and tubes, to transport lipids across the periplasm.

Area of Science:

  • Microbiology
  • Structural Biology
  • Biochemistry

Background:

  • Phospholipid transport between bacterial inner and outer membranes across the periplasm remains poorly understood.
  • The role of the mammalian cell entry (MCE) protein family in this process is unclear.

Purpose of the Study:

  • To elucidate the mechanisms and structures involved in phospholipid trafficking between bacterial membranes.
  • To investigate the role of MCE proteins in mediating lipid transport.

Main Methods:

  • Determining the structures of MCE proteins using electron microscopy (EM).
  • Analyzing the assembly and function of MCE protein complexes in lipid transport.

Main Results:

  • MCE proteins form hexameric assemblies with channels capable of lipid transport.
  • E. coli MCE proteins MlaD, YebT, and PqiB exhibit diverse architectures: MlaD forms a ring with an ABC transporter, YebT forms a stacked ring tube, and PqiB forms a syringe-like structure.
  • YebT and PqiB channels are long enough to span the periplasmic space, facilitating inter-membrane lipid transfer.

Conclusions:

  • The MCE protein family utilizes diverse protein-based channel architectures for lipid transport between bacterial membranes.
  • These findings reveal novel mechanisms for lipid trafficking in bacteria and potentially in eukaryotic organelles.

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