Yool A J, Schwarz T L
Department of Physiology, University of Arizona College of Medicine, Tucson 85724-5051, USA.
Biophys J. 1996 Nov;71(5):2467-72. doi: 10.1016/S0006-3495(96)79440-7.
Mutagenesis of the H5 region of the Shaker K+ channel has provided strong evidence that these amino acids form a major portion of the ionic pore. We have previously observed that a single-site mutation (T441S) in this region increased the apparent relative permeability of the channel to NH4+. We now report that this increased relative permeability to NH4+ is sensitive to small changes in external K+ in a pattern consistent with an anomalous mole fraction effect. The effect is not apparent in the wild-type channel. These findings, in combination with other studies showing effects of this particular mutation on the binding of tetraethylammonium and hydroxylamine, support the hypothesis that T441S alters the affinity of a putative ion binding site for NH4+ and ammonium derivatives. The mutation T441S alters ionic selectivity and reveals the multi-ion nature of the mutant Shaker K+ channel.
对Shaker钾通道H5区域进行诱变已提供了有力证据,表明这些氨基酸构成了离子孔的主要部分。我们之前观察到,该区域的一个单点突变(T441S)增加了通道对NH4 + 的表观相对通透性。我们现在报告,这种对NH4 + 相对通透性的增加对外部K + 的微小变化敏感,其模式与异常摩尔分数效应一致。在野生型通道中未观察到这种效应。这些发现,与其他显示该特定突变对四乙铵和羟胺结合有影响的研究相结合,支持了T441S改变假定离子结合位点对NH4 + 和铵衍生物亲和力的假说。突变T441S改变了离子选择性,并揭示了突变型Shaker钾通道的多离子性质。