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Published on: March 20, 2016
Architecture of the MKK6-p38α complex defines the basis of MAPK specificity and activation
Pauline Juyoux1, Ioannis Galdadas2,3, Dorothea Gobbo2,3
1European Molecular Biology Laboratory (EMBL), Grenoble, France.
Abstract:
The mitogen-activated protein kinase (MAPK) p38α is a central component of signaling in inflammation and the immune response and is, therefore, an important drug target. Little is known about the molecular mechanism of its activation by double phosphorylation from MAPK kinases (MAP2Ks), because of the challenge of trapping a transient and dynamic heterokinase complex. We applied a multidisciplinary approach to generate a structural model of p38α in complex with its MAP2K, MKK6, and to understand the activation mechanism. Integrating cryo-electron microscopy with molecular dynamics simulations, hydrogen-deuterium exchange mass spectrometry, and experiments in cells, we demonstrate a dynamic, multistep phosphorylation mechanism, identify catalytically relevant interactions, and show that MAP2K-disordered amino termini determine pathway specificity. Our work captures a fundamental step of cell signaling: a kinase phosphorylating its downstream target kinase.
Insights
Researchers modeled the activation of p38α (mitogen-activated protein kinase) by MKK6 (MAP2K). This reveals a dynamic, multistep phosphorylation mechanism crucial for immune signaling and drug development.
Area of Science:
- Cellular signaling pathways
- Molecular mechanisms of kinase activation
- Protein-protein interactions in immunity
Background:
- Mitogen-activated protein kinase (MAPK) p38α is a key regulator of inflammation and immune responses.
- p38α is a significant drug target, but its activation mechanism by MAP2Ks remains poorly understood due to transient complex formation.
Purpose of the Study:
- To elucidate the molecular mechanism of p38α activation by its cognate MAP2K, MKK6.
- To generate a structural model of the p38α-MKK6 complex and understand the phosphorylation process.
Main Methods:
- Integrated cryo-electron microscopy (cryo-EM) with molecular dynamics (MD) simulations.
- Utilized hydrogen-deuterium exchange mass spectrometry (HDX-MS) and cellular experiments.
- Developed a multidisciplinary approach to capture transient kinase complexes.
Main Results:
- A dynamic, multistep phosphorylation mechanism for p38α activation was demonstrated.
- Key catalytically relevant interactions within the p38α-MKK6 complex were identified.
- Disordered amino termini of MAP2K were shown to dictate pathway specificity.
Conclusions:
- The study provides unprecedented structural and mechanistic insights into a fundamental kinase-kinase phosphorylation event.
- Understanding this activation mechanism can inform the development of targeted therapeutics for inflammatory and immune diseases.
- MAP2K disordered regions play a critical role in regulating signaling specificity.
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