Peleg Sagit, Varon Dalia, Ivanina Tatiana, Dessauer Carmen W, Dascal Nathan
Department of Physiology and Pharmacology, Sackler School of Medicine, Tel Aviv University, Ramat Aviv, 69978, Israel.
Neuron. 2002 Jan 3;33(1):87-99. doi: 10.1016/s0896-6273(01)00567-0.
GIRK (Kir3) channels are activated by neurotransmitters coupled to G proteins, via a direct binding of G(beta)(gamma). The role of G(alpha) subunits in GIRK gating is elusive. Here we demonstrate that G(alpha)(i) is not only a donor of G(beta)(gamma) but also regulates GIRK gating. When overexpressed in Xenopus oocytes, GIRK channels show excessive basal activity and poor activation by agonist or G(beta)(gamma). Coexpression of G(alpha)(i3) or G(alpha)(i1) restores the correct gating parameters. G(alpha)(i) acts neither as a pure G(beta)(gamma) scavenger nor as an allosteric cofactor for G(beta)(gamma). It inhibits only the basal activity without interfering with G(beta)(gamma)-induced response. Thus, GIRK is regulated, in distinct ways, by both arms of the G protein. G(alpha)(i) probably acts in its GDP bound form, alone or as a part of G(alpha)(beta)(gamma) heterotrimer.
GIRK(Kir3)通道可通过Gβγ的直接结合,被与G蛋白偶联的神经递质激活。Gα亚基在GIRK门控中的作用尚不清楚。在此,我们证明Gαi不仅是Gβγ的供体,还调节GIRK门控。当在非洲爪蟾卵母细胞中过表达时,GIRK通道表现出过高的基础活性,且对激动剂或Gβγ的激活作用不佳。共表达Gαi3或Gαi1可恢复正确的门控参数。Gαi既不作为纯粹的Gβγ清除剂,也不作为Gβγ的变构辅因子。它仅抑制基础活性,而不干扰Gβγ诱导的反应。因此,GIRK受到G蛋白两条臂的不同方式调节。Gαi可能以其结合GDP的形式单独起作用,或作为Gαβγ异源三聚体的一部分起作用。