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Plasma Membrane Vesicles of Opposite Sidedness from Soybean Hypocotyls by Preparative Free-Flow Electrophoresis

机译:通过制备自由流电泳从大豆下胚轴相反的质膜膜囊泡

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摘要

Absolute orientations (sidedness) of plasma membrane vesicles obtained in highly purified fractions by preparative free-flow electrophoresis and by aqueous two-phase partition were determined based on ATPase latency and morphological criteria. Free-flow electrophoresis yielded two plasma membrane fractions. One, the least electronegative and designated fraction `E,' was pure plasma membrane. The other, more electronegative and designated fraction `C,' was heavily contaminated by various other cellular membranes. Plasma membrane vesicles from both fraction C and fraction E partitioned into the upper phase with aqueous two-phase partitioning. Purified plasma membrane obtained from microsomes by two-phase partition (upper phase) when subjected to free-flow electrophoresis also yielded two fractions, one fraction co-migrated with fraction C and another fraction co-migrated with fraction E. Both fractions exhibited an ATPase activity sensitive to vanadate and insensitive to nitrate and azide. ATPase activity was used as a structure-linked latency marker for the inner membrane surface. Concanavalin A binding (linked to peroxidase) was used as an imposed electron microscope marker for the outer membrane surface. Fraction E vesicles showed low ATPase latency (two-fold or less) and weak reactivity with concanavalin A peroxidase. In contrast, fraction C vesicles were characterized by much greater latencies upon detergent treatment (sevenfold) and a strong reaction with concanavalin A peroxidase. Two-phase partition as the initial procedure for plasma membrane isolation, yielded mixtures of vesicles of both inside out and right-side out orientation. Free-flow electrophoresis resolved the plasma membrane isolates into vesicles from fraction C which were right-side out (cytoplasmic side in), and vesicles from fraction E which were wrong-side out (cytoplasmic side out). Therefore, the two methods used in series, provided highly purified membrane preparations of apparently homogenous vesicles of opposite known absolute orientations.
机译:基于ATPase潜伏期和形态学标准,确定了通过制备性自由流电泳和水两相分配在高纯度级分中获得的质膜囊泡的绝对方向(侧面)。自由流动电泳产生两个质膜级分。一个,具有最小负电性和指定分数“ E”的是纯质膜。另一个负电性更高的分数“ C”被各种其他细胞膜严重污染。来自馏分C和馏分E的质膜囊泡通过水两相分配分配到上层相中。在进行自由流动电泳时,通过两相分配(上层)从微粒体中获得的纯化质膜还产生了两个馏分,一个馏分与馏分C共迁移,另一个馏分与馏分E共迁移。两个馏分均显示ATPase对钒酸盐敏感,对硝酸盐和叠氮化物不敏感。 ATPase活性用作内膜表面的结构相关潜伏期标记。伴刀豆球蛋白A结合(连接至过氧化物酶)用作外膜表面的电子显微镜标记。级分E囊泡显示低ATPase潜伏期(两倍或更少),并且与伴刀豆球蛋白A过氧化物酶的反应性较弱。相反,级分C囊泡的特征在于在去污剂处理后的潜伏期大得多(七倍),并且与伴刀豆球蛋白A过氧化物酶强烈反应。两相分配作为质膜分离的初始程序,产生了由内而外和朝外的方向的囊泡混合物。自由流电泳将质膜分离物分离成来自C部分的囊泡,其是右侧朝外(胞质侧朝里),和来自E部分的囊泡,其是反面朝外(胞质侧朝外)。因此,串联使用的两种方法提供了具有相反的已知绝对取向的表面均匀的囊泡的高度纯化的膜制剂。

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