Weinman E J, Shenolikar S, Cragoe E J, Dubinsky W P
Department of Internal Medicine, Pharmacology, and Physiology, University of Texas Medical School, Houston 77225.
J Membr Biol. 1988;101(1):1-9. doi: 10.1007/BF01872814.
In order to permit future characterization and possible isolation of the Na+-H+ exchanger from the apical membrane of proximal tubular cells, studies were performed to solubilize and reconstitute this transporter. Rabbit brush border membranes were prepared by a magnesium aggregation method, solubilized with the detergent octyl glucoside, and reconstituted into artificial phospholipid vesicles. In the presence of a pH gradient (pHin 6.0, pHout 8.0), the uptake of 1 mM 22Na+ into the proteoliposomes was five- to sevenfold higher than into liposomes. Amiloride (2 mM) inhibited proton gradient-stimulated uptake of sodium by 50%. As compared to proton gradient conditions, the uptake of sodium was lower in the absence of a pH gradient but was significantly higher when the outside and inside pH was 6.0 than 8.0. The Ka for sodium in reconstituted proteoliposomes studied under pH gradient conditions was 4 mM. The uptake of sodium in proteoliposomes prepared from heat-denatured membrane proteins was significantly decreased. These studies demonstrate that proteoliposomes prepared from octyl glucoside-solubilized brush border membrane proteins and asolectin exhibit proton gradient-stimulated, amiloride-inhibitable, electroneutral uptake of sodium. The ability to solubilize and reconstitute the Na+-H+ exchanger from the apical membrane of the proximal tubule will be of value in isolating and characterizing this transporter.
为了便于将来对近端肾小管细胞顶端膜上的钠氢交换体进行特性分析并可能将其分离出来,开展了相关研究以溶解并重组这种转运体。兔刷状缘膜通过镁聚集法制备,用去污剂辛基葡糖苷溶解,然后重组到人工磷脂囊泡中。在存在pH梯度(内部pH 6.0,外部pH 8.0)的情况下,蛋白脂质体对1 mM 22Na+的摄取比脂质体高五到七倍。氨氯地平(2 mM)抑制质子梯度刺激的钠摄取达50%。与质子梯度条件相比,在没有pH梯度时钠摄取较低,但当外部和内部pH为6.0时比pH为8.0时显著更高。在pH梯度条件下研究的重组蛋白脂质体中钠的Ka为4 mM。由热变性膜蛋白制备的蛋白脂质体中钠的摄取显著降低。这些研究表明,由辛基葡糖苷溶解的刷状缘膜蛋白和大豆卵磷脂制备的蛋白脂质体表现出质子梯度刺激的、氨氯地平抑制的、电中性的钠摄取。从近端小管顶端膜溶解并重组钠氢交换体的能力对于分离和表征这种转运体将具有价值。