Lin Ting-Feng, Lin I-Wen, Chen Shu-Ching, Wu Hao-Han, Yang Chi-Sheng, Fang Hsin-Yu, Chiu Mei-Miao, Jeng Chung-Jiuan
Institute of Anatomy and Cell Biology, School of Medicine, and National Yang-Ming University, No. 155, Section 2, Li-Non Street, Taipei 12212, Taiwan.
Department of Medical Research, National Taiwan University Hospital, Taipei 10051, Taiwan.
J Biol Chem. 2014 Aug 15;289(33):22815-22834. doi: 10.1074/jbc.M114.574814. Epub 2014 Jul 9.
A functional voltage-gated K(+) (Kv) channel comprises four pore-forming α-subunits, and only members of the same Kv channel subfamily may co-assemble to form heterotetramers. The ether-à-go-go family of Kv channels (KCNH) encompasses three distinct subfamilies: Eag (Kv10), Erg (Kv11), and Elk (Kv12). Members of different ether-à-go-go subfamilies, such as Eag and Erg, fail to form heterotetramers. Although a short stretch of amino acid sequences in the distal C-terminal section has been implicated in subfamily-specific subunit assembly, it remains unclear whether this region serves as the sole and/or principal subfamily recognition domain for Eag and Erg. Here we aim to ascertain the structural basis underlying the subfamily specificity of ether-à-go-go channels by generating various chimeric constructs between rat Eag1 and human Erg subunits. Biochemical and electrophysiological characterizations of the subunit interaction properties of a series of different chimeric and truncation constructs over the C terminus suggested that the putative C-terminal recognition domain is dispensable for subfamily-specific assembly. Further chimeric analyses over the N terminus revealed that the N-terminal region may also harbor a subfamily recognition domain. Importantly, exchanging either the N-terminal or the C-terminal domain alone led to a virtual loss of the intersubfamily assembly boundary. By contrast, simultaneously swapping both recognition domains resulted in a reversal of subfamily specificity. Our observations are consistent with the notion that both the N-terminal and the C-terminal recognition domains are required to sustain the subfamily-specific assembly of rat Eag1 and human Erg.
一个功能性电压门控钾离子(Kv)通道由四个形成孔道的α亚基组成,并且只有同一Kv通道亚家族的成员才能共同组装形成异源四聚体。Kv通道的去极化激活钾通道家族(KCNH)包括三个不同的亚家族:Eag(Kv10)、Erg(Kv11)和Elk(Kv12)。不同的去极化激活钾通道亚家族成员,如Eag和Erg,不能形成异源四聚体。尽管远端C末端区域的一小段氨基酸序列与亚家族特异性亚基组装有关,但尚不清楚该区域是否作为Eag和Erg的唯一和/或主要亚家族识别结构域。在这里,我们旨在通过在大鼠Eag1和人类Erg亚基之间构建各种嵌合构建体,确定去极化激活钾通道亚家族特异性的结构基础。对一系列不同嵌合和截短构建体在C末端的亚基相互作用特性进行生化和电生理表征表明,推定的C末端识别结构域对于亚家族特异性组装是可有可无的。对N末端进行进一步的嵌合分析表明,N末端区域也可能含有一个亚家族识别结构域。重要的是,单独交换N末端或C末端结构域会导致亚家族间组装边界的实际丧失。相比之下,同时交换两个识别结构域会导致亚家族特异性的逆转。我们的观察结果与以下观点一致,即N末端和C末端识别结构域都是维持大鼠Eag1和人类Erg亚家族特异性组装所必需的。