Institut de Biologie Structurale (IBS), Univ. Grenoble Alpes, CEA, CNRS, LabEx ICST, 71, avenue des Martyrs, CS10090, F-38044 Grenoble, France.
Department of Chemistry, King's College London, Britannia House, 7 Trinity Street, London SE1 1DB, UK.
Biochim Biophys Acta Biomembr. 2017 Oct;1859(10):2144-2153. doi: 10.1016/j.bbamem.2017.07.015. Epub 2017 Jul 28.
Ion channel-coupled receptors (ICCRs) are original man-made ligand-gated ion channels created by fusion of G protein-coupled receptors (GPCRs) to the inward-rectifier potassium channel Kir6.2. GPCR conformational changes induced by ligand binding are transduced into electrical current by the ion channel. This functional coupling is closely related to the length of the linker region formed by the GPCR C-terminus (C-ter) and Kir6.2N-terminus (N-ter). Manipulating the GPCR C-ter length allows to finely tune the channel regulation, both in amplitude and sign (opening or closing Kir6.2). In this work, we demonstrate that the primary sequence of the channel N-terminal domain is an additional parameter for the functional coupling with GPCRs. As for all Kir channels, a cluster of basic residues is present in the N-terminal domain of Kir6.2 and is composed of 5 arginines which are proximal to the GPCR C-ter in the fusion proteins. Using a functional mapping approach, we demonstrate the role of specific arginines (R27 and R32) for the function of ICCRs, indicating that the position and not the cluster of positively-charged arginines is critical for the channel regulation by the GPCR. Following observations provided by molecular dynamics simulation, we explore the hypothesis of interaction of these arginines with acidic residues, and using site-directed mutagenesis, we identified aspartate D307 and glutamate E308 residues as critical for the function of ICCRs. These results demonstrate the critical role of the N-terminal and C-terminal charged residues of Kir6.2 for its allosteric regulation by the fused GPCR.
离子通道偶联受体(ICCRs)是通过将 G 蛋白偶联受体(GPCR)与内向整流钾通道 Kir6.2 融合而产生的原始人工配体门控离子通道。配体结合引起的 GPCR 构象变化通过离子通道转导为电流。这种功能偶联与 GPCR C 端(C 端)和 Kir6.2N 端(N 端)形成的连接区的长度密切相关。操纵 GPCR C 端的长度可以精细调节通道的调节,无论是在幅度还是符号(打开或关闭 Kir6.2)上。在这项工作中,我们证明了通道 N 端结构域的一级序列是与 GPCR 进行功能偶联的另一个参数。与所有 Kir 通道一样,Kir6.2 的 N 端结构域存在一个碱性残基簇,由融合蛋白中靠近 GPCR C 端的 5 个精氨酸组成。使用功能映射方法,我们证明了特定精氨酸(R27 和 R32)在 ICCRs 功能中的作用,表明带正电荷的精氨酸的位置而不是簇对于通道由 GPCR 调节是关键的。根据分子动力学模拟的观察结果,我们探讨了这些精氨酸与酸性残基相互作用的假设,并通过定点突变,确定天冬氨酸 D307 和谷氨酸 E308 残基是 ICCRs 功能的关键。这些结果表明 Kir6.2 的 N 端和 C 端带电残基在其由融合 GPCR 进行变构调节中的关键作用。