Lin Yu-Wen, Jia Taiping, Weinsoft Anne M, Shyng Show-Ling
Center for Research on Occupational and Environmental Toxicology, Oregon Health & Science University, Portland, OR 97239, USA.
J Gen Physiol. 2003 Aug;122(2):225-37. doi: 10.1085/jgp.200308822.
ATP-sensitive potassium (KATP) channels are formed by the coassembly of four Kir6.2 subunits and four sulfonylurea receptor subunits (SUR). The cytoplasmic domains of Kir6.2 mediate channel gating by ATP, which closes the channel, and membrane phosphoinositides, which stabilize the open channel. Little is known, however, about the tertiary or quaternary structures of the domains that are responsible for these interactions. Here, we report that an ion pair between glutamate 229 and arginine 314 in the intracellular COOH terminus of Kir6.2 is critical for maintaining channel activity. Mutation of either residue to alanine induces inactivation, whereas charge reversal at positions 229 and 314 (E229R/R314E) abolishes inactivation and restores the wild-type channel phenotype. The close proximity of these two residues is demonstrated by disulfide bond formation between cysteine residues introduced at the two positions (E229C/R314C); disulfide bond formation abolishes inactivation and stabilizes the current. Using Kir6.2 tandem dimer constructs, we provide evidence that the ion pair likely forms by residues from two adjacent Kir6.2 subunits. We propose that the E229/R314 intersubunit ion pairs may contribute to a structural framework that facilitates the ability of other positively charged residues to interact with membrane phosphoinositides. Glutamate and arginine residues are found at homologous positions in many inward rectifier subunits, including the G-protein-activated inwardly rectifying potassium channel (GIRK), whose cytoplasmic domain structure has recently been solved. In the GIRK structure, the E229- and R314-corresponding residues are oriented in opposite directions in a single subunit such that in the tetramer model, the E229 equivalent residue from one subunit is in close proximity of the R314 equivalent residue from the adjacent subunit. The structure lends support to our findings in Kir6.2, and raises the possibility that a homologous ion pair may be involved in the gating of GIRKs.
ATP敏感性钾(KATP)通道由四个Kir6.2亚基和四个磺脲类受体亚基(SUR)共同组装而成。Kir6.2的胞质结构域介导通道的门控,ATP可使通道关闭,而膜磷酸肌醇则使开放的通道稳定。然而,对于负责这些相互作用的结构域的三级或四级结构,人们了解甚少。在此,我们报告Kir6.2细胞内COOH末端的谷氨酸229和精氨酸314之间的离子对对于维持通道活性至关重要。将这两个残基中的任何一个突变为丙氨酸都会诱导失活,而在位置229和314处的电荷反转(E229R/R314E)则会消除失活并恢复野生型通道表型。通过在这两个位置引入的半胱氨酸残基之间形成二硫键,证明了这两个残基的紧密接近;二硫键的形成消除了失活并稳定了电流。使用Kir6.2串联二聚体构建体,我们提供证据表明该离子对可能由两个相邻的Kir6.2亚基的残基形成。我们提出E229/R314亚基间离子对可能有助于形成一个结构框架,促进其他带正电荷的残基与膜磷酸肌醇相互作用的能力。在许多内向整流亚基中,包括最近其胞质结构域结构已被解析的G蛋白激活的内向整流钾通道(GIRK),在同源位置发现了谷氨酸和精氨酸残基。在GIRK结构中,与E229和R314对应的残基在单个亚基中呈相反方向排列,因此在四聚体模型中,一个亚基的E229等效残基与相邻亚基的R314等效残基紧密相邻。该结构支持了我们在Kir6.2中的发现,并增加了同源离子对可能参与GIRK门控的可能性。