Li Ciming, Capendeguy Oihana, Geering Käthi, Horisberger Jean-Daniel
Department of Pharmacology and Toxicology, Faculty of Biology and Medicine, University of Lausanne, Bugnon 27, CH-1005 Lausanne, Switzerland.
Proc Natl Acad Sci U S A. 2005 Sep 6;102(36):12706-11. doi: 10.1073/pnas.0505980102. Epub 2005 Aug 25.
The sodium pump, or Na,K-ATPase, exports three intracellular sodium ions in exchange for two extracellular potassium ions. In the high resolution structure of the related calcium pump, two cation-binding sites have been identified. The two corresponding sites in the sodium pump are expected to be alternatively occupied by sodium and potassium. The position of a third sodium-specific site is still hypothetical. Here, we report the large effects of single residue substitutions on the voltage-dependent kinetics of the release of sodium to the extracellular side of the membrane. These mutations also alter the apparent affinity for intracellular sodium while one of them does not affect the intrinsic affinity for potassium. These results enable us to locate the third sodium-specific site of the sodium pump in a space between the fifth, sixth, and ninth transmembrane helices of the alpha-subunit and provide an experimental validation of the model proposed by Ogawa and Toyoshima [Ogawa, H. & Toyoshima, C. (2002) Proc. Natl. Acad. Sci. USA 99, 15977-15982].
钠泵,即Na,K - ATP酶,将三个细胞内钠离子输出,以交换两个细胞外钾离子。在相关钙泵的高分辨率结构中,已确定了两个阳离子结合位点。钠泵中的两个相应位点预计会被钠和钾交替占据。第三个钠特异性位点的位置仍然是假设性的。在此,我们报告了单个残基取代对膜外侧钠离子释放的电压依赖性动力学的巨大影响。这些突变还改变了对细胞内钠的表观亲和力,而其中一个突变不影响对钾的固有亲和力。这些结果使我们能够将钠泵的第三个钠特异性位点定位在α亚基的第五、第六和第九个跨膜螺旋之间的空间中,并为小川和丰岛提出的模型提供了实验验证[小川,H. & 丰岛,C. (2002) 《美国国家科学院院刊》99, 15977 - 15982]。