Müllner Carmen, Yakubovich Daniel, Dessauer Carmen W, Platzer Dieter, Schreibmayer Wolfgang
Institute for Medical Physics and Biophysics, Graz University, Austria.
Biophys J. 2003 Feb;84(2 Pt 1):1399-409. doi: 10.1016/S0006-3495(03)74954-6.
G-Protein activated, inwardly rectifying potassium channels (GIRKs) are important effectors of G-protein beta/gamma-subunits, playing essential roles in the humoral regulation of cardiac activity and also in higher brain functions. G-protein activation of channels of the GIRK1/GIRK4 heterooligomeric composition is controlled via phosphorylation by cyclic AMP dependent protein kinase (PKA) and dephosphorylation by protein phosphatase 2A (PP(2)A). To study the molecular mechanism of this unprecedented example of G-protein effector regulation, single channel recordings were performed on isolated patches of plasma membranes of Xenopus laevis oocytes. Our study shows that: (i) The open probability (P(o)) of GIRK1/GIRK4 channels, stimulated by coexpressed m(2)-receptors, was significantly increased upon addition of the catalytic subunit of PKA to the cytosolic face of an isolated membrane patch. (ii) At moderate concentrations of recombinant G(beta1/gamma2), used to activate the channel, P(o) was significantly reduced in patches treated with PP(2)A, when compared to patches with PKA-cs. (iii) Several single channel gating parameters, including modal gating behavior, were significantly different between phosphorylated and dephosphorylated channels, indicating different gating behavior between the two forms of the protein. Most of these changes were, however, not responsible for the marked difference in P(o) at moderate G-protein concentrations. (iv) An increase of the frequency of openings (f(o)) and a reduction of dwell time duration of the channel in the long-lasting C(5) state was responsible for facilitation of GIRK1/GIRK4 channels by protein phosphorylation. Dephosphorylation by PP(2)A led to an increase of G(beta1/gamma2) concentration required for full activation of the channel and hence to a reduction of the apparent affinity of GIRK1/GIRK4 for G(beta1/gamma2). (v) Although possibly not directly the target of protein phosphorylation/dephosphorylation, the last 20 C-terminal amino acids of the GIRK1 subunit are required for the reduction of apparent affinity for the G-protein by PP(2)A, indicating that they constitute an essential part of the off-switch.
G蛋白激活的内向整流钾通道(GIRKs)是G蛋白β/γ亚基的重要效应器,在心脏活动的体液调节以及高级脑功能中发挥着重要作用。G蛋白对GIRK1/GIRK4异源寡聚体通道的激活是通过环磷酸腺苷依赖性蛋白激酶(PKA)的磷酸化作用以及蛋白磷酸酶2A(PP(2)A)的去磷酸化作用来控制的。为了研究这种前所未有的G蛋白效应器调节例子的分子机制,我们在非洲爪蟾卵母细胞的分离质膜片上进行了单通道记录。我们的研究表明:(i)共表达的m(2)受体刺激的GIRK1/GIRK4通道的开放概率(P(o)),在向分离膜片的胞质面添加PKA催化亚基后显著增加。(ii)在用于激活通道的重组G(beta1/gamma2)的中等浓度下,与用PKA催化亚基处理的膜片相比,用PP(2)A处理的膜片中P(o)显著降低。(iii)包括模态门控行为在内的几个单通道门控参数,在磷酸化和去磷酸化通道之间有显著差异,表明该蛋白的两种形式之间门控行为不同。然而,这些变化大多与中等G蛋白浓度下P(o)的显著差异无关。(iv)开放频率(f(o))的增加以及通道在持久C(5)状态下停留时间的缩短是蛋白磷酸化促进GIRK1/GIRK4通道的原因。PP(2)A的去磷酸化导致通道完全激活所需的G(beta1/gamma2)浓度增加,从而降低了GIRK1/GIRK4对G(beta1/gamma2)的表观亲和力。(v)尽管可能不是蛋白磷酸化/去磷酸化的直接靶点,但GIRK1亚基的最后20个C末端氨基酸对于PP(2)A降低对G蛋白的表观亲和力是必需的,这表明它们构成了关闭开关的重要部分。