Department of Biological Sciences, Ohio University, Athens, OH 45701, USA.
J Membr Biol. 2010 Jul;236(2):203-14. doi: 10.1007/s00232-010-9293-y. Epub 2010 Aug 10.
The Na(+)/K(+)-ATPase exports 3Na(+) and imports 2K(+) at the expense of the hydrolysis of 1 ATP. In the absence of K(+), it carries on electroneutral, Na(+)-dependent transient charge movement (also known as "electroneutral Na(+)/Na(+) exchange mode") and produces a transient current containing faster and slower components in response to a sudden voltage step. Components with different speeds represent sequential release of Na(+) ions from three binding sites. The effect of holding potential on slow charge movement was studied in the presence of different concentrations of ADP(i), Na (i) (+) and Na (o) (+) with the intention of improving our understanding of Na (i) (+) binding. However, the manipulation of ADP and Na(+) did not cause as pronounced changes as predicted in the magnitude of charge movement (Q (tot)), which indicated that our experimental conditions were not able to backwardly drive reaction across the energy barrier to Na (i) (+) release/rebinding steps. On the contrary, lowering Na(+) caused evident dependence of Q (tot) on holding potential, with characteristics suggesting that pumps were escaping from E2P through the uncoupled Na(+) efflux activity.
钠钾-ATP 酶以消耗 1 分子 ATP 的水解为代价,将 3 个钠离子泵出细胞外,同时将 2 个钾离子泵入细胞内。在没有钾离子的情况下,它会进行电中性的、钠离子依赖的暂态电荷移动(也称为“电中性的钠离子/钠离子交换模式”),并产生一个暂态电流,当突然施加电压阶跃时,该电流包含快和慢两个成分。具有不同速度的成分代表三个结合位点中钠离子的顺序释放。本研究旨在通过改变维持电位来研究 ADP(i)、Na(i)(+)和 Na(o)(+) 不同浓度对慢电荷移动的影响,以加深对 Na(i)(+)结合的理解。然而,与预测的电荷移动幅度(Q(tot))相比,ADP和Na(+)的操纵并没有引起如此明显的变化,这表明我们的实验条件不足以将反应逆向驱动穿过能量障碍,从而导致钠离子释放/再结合步骤。相反,降低Na(+)会导致 Q(tot)对维持电位的明显依赖性,其特征表明泵通过非耦合的钠离子外流活性从 E2P 逃逸。