Oppedisano Francesca, Indiveri Cesare
Department of Cell Biology, University of Calabria, Via P. Bucci 4c, 87036 Arcavacata di Rende, Italy.
Biochim Biophys Acta. 2008 Oct;1778(10):2258-65. doi: 10.1016/j.bbamem.2008.05.011. Epub 2008 Jun 3.
Na+ dependent [3H]glutamine uptake was found in liposomes reconstituted with solubilized rat kidney brush border in the presence of intraliposomal K+. The reconstituted system was optimised with respect to the critical parameters of the cyclic detergent removal procedure, i.e., the detergent used for the solubilization, the protein concentration, the detergent/phospholipid ratio and the number of passages through a single Amberlite column. Time dependent [3H]glutamine accumulation in proteoliposomes occurred only in the presence of external Na+ and internal K+. The transporter showed low if there is any tolerance towards the substitution of Na+ or K+ for other cations. Valinomycin strongly stimulated the transport indicating that it is electrogenic. Intraliposomal glutamine had no effect. From the dependence of the transport rate on the Na+ concentration cooperativity index close to 1 was derived, indicating that 1 Na+ should be involved in the cotransport with glutamine. The electrogenicity of the transport originated from the Na+ transport. Optimal rate of 0.1 mM [3H]glutamine uptake was found in the presence of 50 mM intraliposomal K-gluconate. At higher K-gluconate concentrations the transport rate decreased. The activity of the reconstituted transporter was pH dependent with optimal function in the range pH 6.5-7.0. [3H]glutamine (and [3H]leucine) uptake was inhibited by all the neutral but not by the positively or negatively charged amino acids. The sulfhydryl reagents HgCl2, mersalyl, p-hydroxymercuribenzoate and the substrate analogue 2-aminobicyclo[2,2,1]heptane-2-carboxylate strongly inhibited the transporter, whereas the amino acid analogue alpha-(methylamino)isobutyrate had no effect. The inhibition by mersalyl was protected by the presence of the substrate. On the basis of the Na+ dependence, the electrogenic transport mode and the specificity towards the amino acids, the reconstituted transporter was classified as B degrees-like.
在脂质体内存在K⁺的情况下,在用溶解的大鼠肾刷状缘重构的脂质体中发现了Na⁺依赖性的[³H]谷氨酰胺摄取。针对环状去污剂去除程序的关键参数对重构系统进行了优化,即用于溶解的去污剂、蛋白质浓度、去污剂/磷脂比例以及通过单个 Amberlite 柱的次数。仅在存在外部Na⁺和内部K⁺的情况下,蛋白脂质体中才会出现随时间变化的[³H]谷氨酰胺积累。如果用其他阳离子替代Na⁺或K⁺,转运体对其耐受性很低(如果有的话)。缬氨霉素强烈刺激转运,表明其具有电生性。脂质体内的谷氨酰胺没有影响。从转运速率对Na⁺浓度的依赖性得出协同指数接近1,表明1个Na⁺应参与与谷氨酰胺的共转运。转运的电生性源于Na⁺转运。在存在50 mM脂质体内K - 葡萄糖酸盐的情况下,发现0.1 mM [³H]谷氨酰胺摄取的最佳速率。在较高的K - 葡萄糖酸盐浓度下,转运速率降低。重构转运体的活性依赖于pH,在pH 6.5 - 7.0范围内功能最佳。[³H]谷氨酰胺(和[³H]亮氨酸)的摄取受到所有中性氨基酸的抑制,但不受带正电荷或负电荷氨基酸的抑制。巯基试剂HgCl₂、汞撒利、对羟基汞苯甲酸和底物类似物2 - 氨基双环[2,2,1]庚烷 - 2 - 羧酸盐强烈抑制转运体,而氨基酸类似物α - (甲基氨基)异丁酸没有影响。汞撒利的抑制作用可被底物的存在所保护。基于Na⁺依赖性、电生性转运模式和对氨基酸的特异性,重构的转运体被归类为B类样。