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蛋白激酶C通过与神经元支架蛋白PICK1相互作用来调节AMPA受体辅助蛋白Shisa9/CKAMP44。

Protein kinase C regulates AMPA receptor auxiliary protein Shisa9/CKAMP44 through interactions with neuronal scaffold PICK1.

作者信息

Kunde Stella-Amrei, Rademacher Nils, Zieger Hanna, Shoichet Sarah A

机构信息

Neuroscience Research Center/Institute of Biochemistry Charité - Universitätsmedizin Berlin Germany.

出版信息

FEBS Open Bio. 2017 Aug 15;7(9):1234-1245. doi: 10.1002/2211-5463.12261. eCollection 2017 Sep.

Abstract

Synaptic α-amino-3-hydroxyl-5-methyl-4-isoxazole-propionate (AMPA) receptors are essential mediators of neurotransmission in the central nervous system. Shisa9/cysteine-knot AMPAR modulating protein 44 (CKAMP44) is a transmembrane protein recently found to be present in AMPA receptor-associated protein complexes. Here, we show that the cytosolic tail of Shisa9/CKAMP44 interacts with multiple scaffold proteins that are important for regulating synaptic plasticity in central neurons. We focussed on the interaction with the scaffold protein PICK1, which facilitates the formation of a tripartite complex with the protein kinase C (PKC) and thereby regulates phosphorylation of Shisa9/CKAMP44 C-terminal residues. This work has implications for our understanding of how PICK1 modulates AMPAR-mediated transmission and plasticity and also highlights a novel function of PKC.

摘要

突触α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)受体是中枢神经系统神经传递的重要介质。Shisa9/半胱氨酸结AMPA受体调节蛋白44(CKAMP44)是一种最近发现存在于AMPA受体相关蛋白复合物中的跨膜蛋白。在此,我们表明Shisa9/CKAMP44的胞质尾部与多种支架蛋白相互作用,这些支架蛋白对于调节中枢神经元的突触可塑性很重要。我们聚焦于与支架蛋白PICK1的相互作用,PICK1促进与蛋白激酶C(PKC)形成三方复合物,从而调节Shisa9/CKAMP44 C末端残基的磷酸化。这项工作对于我们理解PICK1如何调节AMPA受体介导的传递和可塑性具有重要意义,同时也突出了PKC的一种新功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7529/5586339/5e97e679cf27/FEB4-7-1234-g001.jpg

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