4.6 Article

Steps for Shigella Gatekeeper Protein MxiC Function in Hierarchical Type III Secretion Regulation

Journal

JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 292, Issue 5, Pages 1705-1723

Publisher

AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M116.746826

Keywords

biophysics; cellular regulation; electron paramagnetic resonance (EPR); Gram-negative bacteria; molecular genetics; protein secretion; type III secretion system (T3SS); MxiC; Shigella

Funding

  1. Centenary Postgraduate Fund at the University of Bristol
  2. United Kingdom Wellcome Trust [WT088266]
  3. UK Medical Research Council [MR-J002097-1]
  4. Universite Pierre et Marie Curie (Paris 6)
  5. MRC [MR/J002097/1] Funding Source: UKRI
  6. Medical Research Council [MR/J002097/1] Funding Source: researchfish

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Type III secretion systems are complex nanomachines used for injection of proteins from Gram-negative bacteria into eukaryotic cells. Although they are assembled when the environmental conditions are appropriate, they only start secreting upon contact with a host cell. Secretion is hierarchical. First, the pore-forming translocators are released. Second, effector proteins are injected. Hierarchy between these protein classes is mediated by a conserved gatekeeper protein, MxiC, in Shigella. As its molecular mechanism of action is still poorly understood, we used its structure to guide site-directed mutagenesis and to dissect its function. We identified mutants predominantly affecting all known features of MxiC regulation as follows: secretion of translocators, MxiC and/or effectors. Using molecular genetics, we then mapped at which point in the regulatory cascade the mutants were affected. Analysis of some of these mutants led us to a set of electron paramagnetic resonance experiments that provide evidence that MxiC interacts directly with IpaD. We suggest how this interaction regulates a switch in its conformation that is key to its functions.

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