Structural Basis for the Subversion of MAP Kinase Signaling by an Intrinsically Disordered Parasite Secreted Agonist

Erika Pellegrini (1) , Andres Palencia (2) , Laurence Braun (2) , Ulrike Kapp (3) , Alexandre Bougdour (2) , Hassan Belrhali (1, 4) , Matthew W. Bowler (1, 4) , Mohamed-Ali Hakimi (2)

1 EMBL - European Molecular Biology Laboratory [Grenoble]
2 IAB - Institute for Advanced Biosciences / Institut pour l'Avancée des Biosciences (Grenoble)
3 ESRF - European Synchrotron Radiation Facility
4 IBS - UMR 5075 - Institut de biologie structurale

The causative agent of toxoplasmosis, the intracellular parasite Toxoplasma gondii, delivers a protein, GRA24, into the cells it infects that interacts with the mitogen-activated protein (MAP) kinase p38 alpha (MAPK14), leading to activation and nuclear translocation of the host kinase and a subsequent inflammatory response that controls the progress of the parasite. The purification of a recombinant complex of GRA24 and human p38 alpha has allowed the molecular basis of this activation to be determined. GRA24 is shown to be intrinsically disordered, binding two kinases that act independently, and is the only factor required to bypass the canonical mitogen-activated protein kinase activation pathway. An adapted kinase interaction motif (KIM) forms a highly stable complex that competes with cytoplasmic regulatory partners. In addition, the recombinant complex forms a powerful in vitro tool to evaluate the specificity and effectiveness of p38 alpha inhibitors that have advanced to clinical trials, as it provides a hitherto unavailable stable and highly active form of p38 alpha

Domaines: Sciences du Vivant [q-bio]

Erika Pellegrini, Andres Palencia, Laurence Braun, Ulrike Kapp, Alexandre Bougdour, et al.. Structural Basis for the Subversion of MAP Kinase Signaling by an Intrinsically Disordered Parasite Secreted Agonist. Structure (London, England : 1993), 2017, 25 (1), pp.16-26. ⟨10.1016/j.str.2016.10.011⟩. ⟨hal-01691846⟩