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脂肪细胞富含高尔基体部分中葡萄糖转运活性的部分特性

Partial characterization of the glucose transport activity in the Golgi-rich fraction of fat cells.

作者信息

Smith M M, Robinson F W, Watanabe T, Kono T

出版信息

Biochim Biophys Acta. 1984 Aug 22;775(2):121-8. doi: 10.1016/0005-2736(84)90162-7.

Abstract

The glucose transport activity solubilized from the basal and plus insulin forms of the Golgi-rich fraction of adipocytes was partially characterized, and the results were compared with those of the activity obtained from the plus insulin form of the plasma membrane-rich fraction. The transport activity was determined in a cell-free, reconstituted, system. Prior to reconstitution, the activities in the three preparations were all (a) stable at 0 degrees C for at least 4 h, but not at 37 degrees C or above; (b) most stable at pH 7-9, and (c) less stable in Tes than in Tris buffer. After reconstitution, the three activities were all (d) stable at 0 degrees C, (e) most active at pH 5.5, (f) mildly stimulated by divalent cations, (g) unaffected by insulin or 1 mM of several SH-blocking agents, (h) inhibited by heavy metal ions, 10-100 mM of monovalent salts, organic solvents, several sugar isomers, and specific sugar-transport inhibitors. The rates of D-glucose uptake by the three liposome preparations were all inhibited more strongly by 2-deoxy-D-glucose or 3-O-methyl-D-glucose than by D-glucose. These data indicate that the general properties of the glucose transport activity in the Golgi-rich fraction are similar to those of the activity in the plasma membrane-rich fraction.

摘要

对从富含高尔基体的脂肪细胞组分的基础形式和加胰岛素形式中溶解的葡萄糖转运活性进行了部分表征,并将结果与从富含质膜的组分的加胰岛素形式中获得的活性结果进行了比较。在无细胞的重组系统中测定转运活性。在重组之前,三种制剂中的活性均:(a) 在0℃至少4小时稳定,但在37℃或更高温度下不稳定;(b) 在pH 7-9时最稳定,并且(c) 在Tes缓冲液中比在Tris缓冲液中稳定性更低。重组后,三种活性均:(d) 在0℃稳定,(e) 在pH 5.5时最活跃,(f) 受到二价阳离子的轻度刺激,(g) 不受胰岛素或1 mM几种SH阻断剂的影响,(h) 受到重金属离子、10-100 mM单价盐、有机溶剂、几种糖异构体和特定糖转运抑制剂的抑制。三种脂质体制剂对D-葡萄糖的摄取速率均受到2-脱氧-D-葡萄糖或3-O-甲基-D-葡萄糖的抑制比受到D-葡萄糖的抑制更强。这些数据表明,富含高尔基体的组分中葡萄糖转运活性的一般特性与富含质膜的组分中活性的一般特性相似。

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