Yakubovich Daniel, Rishal Ida, Dascal Nathan
Department of Physiology and Pharmacology, Sackler School of Medicine, Tel Aviv University, Ramat Aviv 69978, Israel.
J Mol Neurosci. 2005;25(1):7-19. doi: 10.1385/JMN:25:1:007.
G protein-activated K(+)(GIRK) channels are activated by numerous neurotransmitters that act on Gi/o proteins, via a direct interaction with the Gbetagamma subunit of G proteins. In addition, GIRK channels are positively regulated by intracellular Na(+) via a direct interaction (fast pathway) and via a GGbetagamma-dependent mechanism (slow pathway). The slow modulation has been proposed to arise from the recently described phenomenon of Na(+)-induced reduction of affinity of interaction between GalphaGDP and Gbetagamma subunits of G proteins. In this scenario, elevated Na(+) enhances basal dissociation of G protein heterotrimers, elevating free cellular Gbetagamma and activating GIRK. However, it is not clear whether this hypothesis can account for the quantitative and kinetic aspects of the observed regulation. Here, we report the development of a quantitative model of slow, Na(+)-dependent, G protein-mediated activation of GIRK. Activity of GIRK1F137S channels, which are devoid of direct interaction with Na(+), was measured in excised membrane patches and used as an indicator of free GGbetagamma levels. The change in channel activity was used to calculate the Na(+)-dependent change in the affinity of G protein subunit interaction. Under a wide range of initial conditions, the model predicted that a relatively small decrease in the affinity of interaction of GalphaGDP and GGbetagamma (about twofold under most conditions) accounts for the twofold activation of GIRK induced by Na(+), in agreement with biochemical data published previously. The model also correctly described the slow time course of Na(+) effect and explained the previously observed enhancement of Na(+)-induced activation of GIRK by coexpressed Galphai3. This is the first quantitative model that describes the basal equilibrium between free and bound G protein subunits and its consequences on regulation of a GGbetagamma effector.
G蛋白激活的钾离子(GIRK)通道可被多种作用于Gi/o蛋白的神经递质激活,通过与G蛋白的Gβγ亚基直接相互作用来实现。此外,GIRK通道受细胞内钠离子正向调节,通过直接相互作用(快速途径)和依赖Gβγ的机制(缓慢途径)。有人提出,缓慢调节源于最近描述的钠离子诱导G蛋白的GαGDP与Gβγ亚基之间相互作用亲和力降低的现象。在这种情况下,升高的钠离子增强了G蛋白异源三聚体的基础解离,提高了游离细胞Gβγ水平并激活了GIRK。然而,尚不清楚该假说是否能解释所观察到的调节的定量和动力学方面。在此,我们报告了一种关于缓慢的、钠离子依赖性的、G蛋白介导的GIRK激活的定量模型的建立。在切除的膜片上测量了与钠离子无直接相互作用的GIRK1F137S通道的活性,并将其用作游离Gβγ水平的指标。通道活性的变化用于计算G蛋白亚基相互作用亲和力的钠离子依赖性变化。在广泛的初始条件下,该模型预测GαGDP与Gβγ相互作用亲和力相对较小的降低(大多数情况下约为两倍)可解释钠离子诱导的GIRK两倍激活,这与先前发表的生化数据一致。该模型还正确描述了钠离子效应的缓慢时间进程,并解释了先前观察到的共表达Gαi3增强钠离子诱导的GIRK激活现象。这是第一个描述游离和结合的G蛋白亚基之间基础平衡及其对Gβγ效应器调节后果的定量模型。