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Journal Articles Nature Communications Year : 2018

RIP2 filament formation is required for NOD2 dependent NF-κB signalling

Ambroise Desfosses
Arndt Wallmann
  • Function : Author
Wiebke Manuela Schulze
  • Function : Author
Luca Signor
Grasilda Zenkeviciute
  • Function : Author
Michael Hons
  • Function : Author
Hélène Malet
Irina Gutsche
Guy Schoehn


Activation of the innate immune pattern recognition receptor NOD2 by the bacterial muramyl-dipeptide peptidoglycan fragment triggers recruitment of the downstream adaptor kinase RIP2, eventually leading to NF-κB activation and proinflammatory cytokine production. Here we show that full-length RIP2 can form long filaments mediated by its caspase recruitment domain (CARD), in common with other innate immune adaptor proteins. We further show that the NOD2 tandem CARDs bind to one end of the RIP2 CARD filament, suggesting a mechanism for polar filament nucleation by activated NOD2. We combine X-ray crystallography, solid-state NMR and high-resolution cryo-electron microscopy to determine the atomic structure of the helical RIP2 CARD filament, which reveals the intermolecular interactions that stabilize the assembly. Using structure-guided mutagenesis, we demonstrate the importance of RIP2 polymerization for the activation of NF-κB signalling by NOD2. Our results could be of use to develop new pharmacological strategies to treat inflammatory diseases characterised by aberrant NOD2 signalling.
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Dates and versions

hal-01889011 , version 1 (24-11-2020)



Erika Pellegrini, Ambroise Desfosses, Arndt Wallmann, Wiebke Manuela Schulze, Kristina Rehbein, et al.. RIP2 filament formation is required for NOD2 dependent NF-κB signalling. Nature Communications, 2018, 9 (1), ⟨10.1038/s41467-018-06451-3⟩. ⟨hal-01889011⟩
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