Suzuki M, Takahashi K, Ikeda M, Hayakawa H, Ogawa A, Kawaguchi Y, Sakai O
Department of Pharmacology, Jichi Medical School, Tochigi, Japan.
Nature. 1994 Feb 17;367(6464):642-5. doi: 10.1038/367642a0.
The mammalian renal collecting ducts are responsible for secreting potassium ions into the urine and are a major regulatory site for potassium homeostasis, in which a voltage-independent pH-sensitive K+ channel in the apical membrane plays a central role. Here we describe a complementary DNA encoding a novel K+ channel from rabbit renal cortical collecting tubule cells (RACTK1). RACTK1 has the functional characteristics of the apical K(+)-permeable channel and consists of 284 amino acids, putatively with two transmembrane segments. The sequence of RACTK1, however, shows no homology to known voltage-dependent or -independent K+ channels, and has a different K(+)-driving path and regulatory sites. The study of this protein should provide insight into K+ homeostasis and diseases of K+ metabolism.
哺乳动物的肾集合管负责将钾离子分泌到尿液中,是钾离子稳态的主要调节部位,其中顶端膜上的一种电压非依赖性pH敏感钾通道起着核心作用。在此,我们描述了一种来自兔肾皮质集合管细胞的新型钾通道(RACTK1)的互补DNA。RACTK1具有顶端钾离子通透通道的功能特性,由284个氨基酸组成,推测有两个跨膜区段。然而,RACTK1的序列与已知的电压依赖性或非依赖性钾通道没有同源性,并且具有不同的钾离子驱动途径和调节位点。对这种蛋白质的研究将有助于深入了解钾离子稳态及钾代谢疾病。