Structural mechanism of WASP activation by the enterohaemorrhagic E. coli effector EspFU

Hui-Chun Cheng, Brian M. Skehan, Kenneth G. Campellone, John M. Leong and Michael K. Rosen ()
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Hui-Chun Cheng: University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA
Brian M. Skehan: University of Massachusetts Medical School, Worcester, Massachusetts 01655, USA
Kenneth G. Campellone: University of Massachusetts Medical School, Worcester, Massachusetts 01655, USA
John M. Leong: University of Massachusetts Medical School, Worcester, Massachusetts 01655, USA
Michael K. Rosen: University of Texas Southwestern Medical Center, Dallas, Texas 75390, USA

Nature, 2008, vol. 454, issue 7207, 1009-1013

Abstract: Abstract During infection, enterohaemorrhagic Escherichia coli (EHEC) takes over the actin cytoskeleton of eukaryotic cells by injecting the EspFU protein into the host cytoplasm1,2. EspFU controls actin by activating members of the Wiskott–Aldrich syndrome protein (WASP) family1,2,3,4,5. Here we show that EspFU binds to the autoinhibitory GTPase binding domain (GBD) in WASP proteins and displaces it from the activity-bearing VCA domain (for verprolin homology, central hydrophobic and acidic regions). This interaction potently activates WASP and neural (N)-WASP in vitro and induces localized actin assembly in cells. In the solution structure of the GBD–EspFU complex, EspFU forms an amphipathic helix that binds the GBD, mimicking interactions of the VCA domain in autoinhibited WASP. Thus, EspFU activates WASP by competing directly for the VCA binding site on the GBD. This mechanism is distinct from that used by the eukaryotic activators Cdc42 and SH2 domains, which globally destabilize the GBD fold to release the VCA6,7,8. Such diversity of mechanism in WASP proteins is distinct from other multimodular systems, and may result from the intrinsically unstructured nature of the isolated GBD and VCA elements. The structural incompatibility of the GBD complexes with EspFU and Cdc42/SH2, plus high-affinity EspFU binding, enable EHEC to hijack the eukaryotic cytoskeletal machinery effectively.

Date: 2008
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DOI: 10.1038/nature07160

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