The Interaction between the Drosophila EAG Potassium Channel and the Protein Kinase CaMKII Involves an Extensive Interface at the Active Site of the Kinase. Issue 24 (7th December 2018)

• Record Type: Journal Article
• Authors: Castro-Rodrigues, Artur F.; Zhao, Yaxian; Fonseca, Fátima; Gabant, Guillaume; Cadene, Martine; Robertson, Gail A.; Morais-Cabral, João H.
• Is Part Of: Journal of molecular biology. Volume 430:Issue 24(2018)
• Page Start: 5029
• Page End: 5049
• Publication Date: 2018-12-07
• Subjects: channel–kinase interaction -- NMDA receptor -- kinase–substrate structure -- isothermal calorimetry; dEAG Drosophila EAG -- CaMKII calmodulin-dependent protein kinase II -- RS regulatory segment -- ITC isothermal titration calorimetry -- MBP maltose-binding protein -- PHK phosphorylase kinase -- NADH nicotinamide adenine dinucleotide, reduced; Molecular biology -- Periodicals; Biology -- Periodicals; Biochemistry -- Periodicals; Bacteriology -- Periodicals; Molecular Biology -- Periodicals; Biochemistry -- Periodicals; Biologie moléculaire -- Périodiques; Biologie -- Périodiques; Biochimie -- Périodiques; Moleculaire biologie; Biochemistry; Biology; Molecular biology; Periodicals; 572.805
• DOI: 10.1016/j.jmb.2018.10.015
• Languages: English
• ISSNs: 0022-2836

Abstract

Abstract: The Drosophila EAG ( d EAG) potassium channel is the founding member of the superfamily of KNCH channels, which are involved in cardiac repolarization, neuronal excitability and cellular proliferation. In flies, d EAG is involved in regulation of neuron firing and assembles with CaMKII to form a complex implicated in memory formation. We have characterized the interaction between the kinase domain of CaMKII and a 53-residue fragment of the d EAG channel that includes a canonical CaMKII recognition sequence. Crystal structures together with biochemical/biophysical analysis show a substrate–kinase complex with an unusually tight and extensive interface that appears to be strengthened by phosphorylation of the channel fragment. Electrophysiological recordings show that catalytically active CaMKII is required to observe active d EAG channels. A previously identified phosphorylation site in the recognition sequence is not the substrate for this crucial kinase activity, but rather contributes importantly to the tight interaction of the kinase with the channel. The available data suggest that the d EAG channel is a docking platform for the kinase and that phosphorylation of the channel's kinase recognition sequence modulates the strength of the interaction between the channel and the kinase. Graphical Abstract: Highlights: The d EAG channel forms a complex with the CaMKII kinase in neuron synapses. Crystal structure shows the channel fragment bound to the active site of kinase. Interaction is very tight for a kinase/protein-substrate pair (~ 200-fold tighter). Observation of active d EAG channels requires catalytically active CaMKII. Phosphorylation at T787 in d EAG modulates the interaction with the kinase.