Ganapathy V, Ganapathy M E, Tiruppathi C, Miyamoto Y, Mahesh V B, Leibach F H
Department of Cell and Molecular Biology, Medical College of Georgia, Augusta 30912.
Biochem J. 1988 Jan 1;249(1):179-84. doi: 10.1042/bj2490179.
Brush-border membrane vesicles isolated from normal human term placentas were shown to accumulate succinate transiently against a concentration gradient, when an inward-directed Na+ gradient was imposed across the membrane. This uptake was almost totally due to transport into intravesicular space, non-specific binding to the membranes being negligible. The dependence of the initial uptake rate of succinate on Na+ concentration exhibited sigmoidal kinetics, indicating interaction of more than one Na+ ion with the carrier system. The Hill coefficient for this ion was calculated to be 2.7. The Na+-dependent uptake of succinate was electrogenic, resulting in the transfer of positive charge across the membrane. Kinetic analysis showed that succinate uptake in these vesicles occurred via a single transport system, with an apparent affinity constant of 4.8 +/- 0.2 microM and a maximal velocity of 274 +/- 4 pmol/20 s per mg of protein. Uptake of succinate was strongly inhibited by various C4 or C5 dicarboxylic acids, whereas monocarboxylic acids, amino acids and glucose showed little or no effect. Li+ and K+ could not substitute for Na+ in the uptake process. Instead, Li+ was found to have a significant inhibitory effect on the Na+-dependent uptake of succinate.
从正常足月人胎盘中分离出的刷状缘膜囊泡,当跨膜施加内向的Na⁺梯度时,会显示出短暂地逆浓度梯度积累琥珀酸。这种摄取几乎完全是由于转运到囊泡内空间,与膜的非特异性结合可忽略不计。琥珀酸的初始摄取速率对Na⁺浓度的依赖性呈现S形动力学,表明不止一个Na⁺离子与载体系统相互作用。该离子的希尔系数经计算为2.7。琥珀酸的Na⁺依赖性摄取是生电的,导致正电荷跨膜转移。动力学分析表明,这些囊泡中琥珀酸的摄取通过单一转运系统发生,表观亲和常数为4.8±0.2微摩尔,最大速度为每毫克蛋白质274±4皮摩尔/20秒。琥珀酸的摄取受到各种C4或C5二羧酸的强烈抑制,而单羧酸、氨基酸和葡萄糖的影响很小或没有影响。Li⁺和K⁺在摄取过程中不能替代Na⁺。相反,发现Li⁺对琥珀酸的Na⁺依赖性摄取有显著抑制作用。