Membrane Protein Complex ExbB <sub>4</sub> -ExbD <sub>1</sub> -TonB <sub>1</sub> from Escherichia coli Demonstrates Conformational Plasticity

Aleksandr Sverzhinsky, Jacqueline W. Chung, Justin C. Deme, Lucien Fabre, Kristian T. Levey, Maria Plesa, David M. Carter, Patrick Lypaczewski, James W. Coulton

Journal of Bacteriology · 2015 · 25 citations · 76 references

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Abstract

Receptors in the OM of Gram-negative bacteria allow entry of iron-bound siderophores that are necessary for pathogenicity. Numerous iron-acquisition strategies rely upon a ubiquitous and unique protein for energization: TonB. Complexed with ExbB and ExbD, the Ton system links the PMF to OM transport. Blocking iron uptake by targeting a vital nanomachine holds promise in therapeutics. Despite much research, the stoichiometry, structural arrangement, and molecular mechanism of the CM-embedded ExbB-ExbD-TonB complex remain unreported. Here we demonstrate in vitro evidence of ExbB₄-ExbD₁-TonB₁ complexes. Using 3D EM, we reconstructed the complex in three conformational states that show variable ExbD-TonB heterodimerization. Our structural observations form the basis of a model for TonB-mediated iron acquisition.

References

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