首页> 外文期刊>Biochimica et biophysica acta. Biomembranes >Reconstitution into liposomes of the B degrees -like glutamine-neutral amino acid transporter from renal cell plasma membrane.
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Reconstitution into liposomes of the B degrees -like glutamine-neutral amino acid transporter from renal cell plasma membrane.

机译:从肾细胞质膜重构为B度样谷氨酰胺中性氨基酸转运蛋白的脂质体。

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摘要

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.
机译:在脂质体内K +存在的情况下,在溶解有大鼠肾刷缘的脂质体中发现了Na +依赖性的[3H]谷氨酰胺摄取。相对于循环去污剂去除程序的关键参数,即用于增溶的去污剂,蛋白质浓度,去污剂/磷脂比率和通过单个Amberlite柱的通过次数,对重构系统进行了优化。时间依赖性[3H]谷氨酰胺在脂质体中的积累仅在存在外部Na +和内部K +的情况下发生。如果对Na +或K +替代其他阳离子有任何容忍度,则转运蛋白显示为低。 Valinomycin强烈刺激了转运,表明它是电动的。脂质体内谷氨酰胺没有作用。从传输速率对Na +浓度协同指数的依赖性得出接近于1的结果,表明1 Na +应与谷氨酰胺共转运。转运的电原性源自Na +转运。在50 mM脂质体内K-葡萄糖酸盐存在下,最佳摄取0.1 mM [3H]谷氨酰胺的速率。在较高的葡萄糖酸钾浓度下,转运速率降低。重组转运蛋白的活性取决于pH,在pH 6.5-7.0范围内具有最佳功能。 [3H]谷氨酰胺(和[3H]亮氨酸)的摄取被所有中性的抑制,但不被带正电或带负电的氨基酸抑制。巯基试剂HgCl2,巯基,对羟基巯基苯甲酸酯和底物类似物2-氨基双环[2,2,1]庚烷-2-羧酸盐强烈抑制转运蛋白,而氨基酸类似物α-(甲基氨基)异丁酸酯则没有作用。底物的存在保护了巯基的抑制作用。根据Na +依赖性,电迁移方式和对氨基酸的特异性,将重构的转运蛋白分类为B度样。

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