Hoshi Naoto, Langeberg Lorene K, Scott John D
Howard Hughes Medical Institute, Vollum Institute, Oregon Health and Science University, 3181 S.W. Sam Jackson Park Road, Portland, OR 97239, USA.
Nat Cell Biol. 2005 Nov;7(11):1066-73. doi: 10.1038/ncb1315.
Specificity in cell signalling can be influenced by the targeting of different enzyme combinations to substrates. The A-kinase anchoring protein AKAP79/150 is a multivalent scaffolding protein that coordinates the subcellular localization of second-messenger-regulated enzymes, such as protein kinase A, protein kinase C and protein phosphatase 2B. We developed a new strategy that combines RNA interference of the endogenous protein with a protocol that selects cells that have been rescued with AKAP79/150 forms that are unable to anchor selected enzymes. Using this approach, we show that AKAP79/150 coordinates different enzyme combinations to modulate the activity of two distinct neuronal ion channels: AMPA-type glutamate receptors and M-type potassium channels. Utilization of distinct enzyme combinations in this manner provides a means to expand the repertoire of cellular events that the same AKAP modulates.
细胞信号传导的特异性可受不同酶组合作用于底物的影响。A激酶锚定蛋白AKAP79/150是一种多价支架蛋白,可协调第二信使调节酶的亚细胞定位,如蛋白激酶A、蛋白激酶C和蛋白磷酸酶2B。我们开发了一种新策略,将内源性蛋白的RNA干扰与一种方案相结合,该方案用于筛选已被无法锚定特定酶的AKAP79/150形式拯救的细胞。使用这种方法,我们表明AKAP79/150协调不同的酶组合来调节两种不同的神经元离子通道的活性:AMPA型谷氨酸受体和M型钾通道。以这种方式利用不同的酶组合提供了一种扩展同一AKAP调节的细胞事件种类的方法。