Takenawa T, Wada E, Tsumita T
Biochim Biophys Acta. 1977 Jan 4;464(1):108-17. doi: 10.1016/0005-2736(77)90374-1.
Using hypotonically treated brush border membranes, binding and transport of myo-inositol were examined. By hypotonic treatment, both total and non-specific uptake decreased significantly, but specific uptake was not affected. myo-Inositol release from membranes preloaded by incubation for 2 min was very rapid and about 98% of preloaded myo-inositol was released in 5 min of incubation. However, myo-inositol release from membranes preloaded by incubation for 20 min was fairly slow and 50% of myo-inositol remained in the membranes even after 10 min of incubation. Uptake of myo-inositol decreased by the increase of osmolarity in the medium. However, effect of osmolarity on the uptake was less significant when myo-inositol concentration was lower. Under conditions in which mainly binding occurred, myo-inositol binding to the membranes was measured. Two binding systems were demonstrated and high affinity site could bind 22 pmol/mg protein at most and the apparent Km value was 8.3 muM. Both binding and transport processes were dependent on Na+ and enhanced by Na+-gradient.
使用经低渗处理的刷状缘膜,检测了肌醇的结合和转运情况。通过低渗处理,总摄取量和非特异性摄取量均显著降低,但特异性摄取不受影响。经2分钟孵育预加载的膜中肌醇的释放非常迅速,在孵育5分钟内约98%的预加载肌醇被释放。然而,经20分钟孵育预加载的膜中肌醇的释放相当缓慢,即使在孵育10分钟后仍有50%的肌醇保留在膜中。培养基渗透压的升高会降低肌醇的摄取。然而,当肌醇浓度较低时,渗透压对摄取的影响较小。在主要发生结合的条件下,测定了肌醇与膜的结合情况。证明了两种结合系统,高亲和力位点最多可结合22 pmol/mg蛋白质,表观Km值为8.3 μM。结合和转运过程均依赖于Na+,并由Na+梯度增强。