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钙/钙调蛋白依赖性蛋白激酶II与突触后致密物中NMDA受体的NR2A/B亚基相关联。

Calcium/calmodulin-dependent protein kinase II is associated with NR2A/B subunits of NMDA receptor in postsynaptic densities.

作者信息

Gardoni F, Caputi A, Cimino M, Pastorino L, Cattabeni F, Di Luca M

机构信息

Institute of Pharmacological Sciences, University of Milano, Italy.

出版信息

J Neurochem. 1998 Oct;71(4):1733-41. doi: 10.1046/j.1471-4159.1998.71041733.x.

Abstract

NMDA receptors and Ca2+/calmodulin-dependent kinase II (CaMKII) have been reported to be highly concentrated in the postsynaptic density (PSD). Although the possibility that CaMKII in PSD might be associated with specific proteins has been put forward, the protein or proteins determining the targeting of the kinase in PSD have not yet been identified. Here we report that CaMKII binds to NR2A and NR2B subunits of NMDA receptors in PSD isolated from cortex and hippocampus. The association of NMDA receptor subunits and CaMKII was assessed by immunoprecipitating PSD proteins with antibodies specific for NR2A/B and CaMKII: CaMKII coprecipitated with NR2A/B and NR1 but not with other glutamate ionotropic receptor subunits, such as GluR1 and GluR2-3. A direct association between CaMKII and NR2A/B subunits was further confirmed by overlay experiments using either 32P-autophosphorylated CaMKII or 32P-NR2A/B and by evaluating the formation of a CaMKII-NR2A/B complex by means of the cross-linker disuccimidyl suberate. These data demonstrate an association between the NMDA receptor complex and CaMKII in the postsynaptic compartment, suggesting that this colocalization may be relevant for synaptic plasticity.

摘要

据报道,N-甲基-D-天冬氨酸(NMDA)受体和Ca2+/钙调蛋白依赖性激酶II(CaMKII)高度集中于突触后致密部(PSD)。尽管有人提出PSD中的CaMKII可能与特定蛋白质有关,但尚未确定决定该激酶在PSD中靶向定位的蛋白质。在此,我们报告CaMKII与从皮层和海马体分离的PSD中的NMDA受体的NR2A和NR2B亚基结合。通过用针对NR2A/B和CaMKII的特异性抗体免疫沉淀PSD蛋白来评估NMDA受体亚基与CaMKII的关联:CaMKII与NR2A/B和NR1共沉淀,但不与其他谷氨酸离子型受体亚基共沉淀,如GluR1和GluR2-3。使用32P-自磷酸化的CaMKII或32P-NR2A/B的覆盖实验以及通过交联剂辛二酸二琥珀酰亚胺酯评估CaMKII-NR2A/B复合物的形成,进一步证实了CaMKII与NR2A/B亚基之间的直接关联。这些数据证明了突触后区室中NMDA受体复合物与CaMKII之间的关联,表明这种共定位可能与突触可塑性相关。

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