Kasanicki M A, Cairns M T, Davies A, Gardiner R M, Baldwin S A
Department of Biochemistry and Chemistry, Royal Free Hospital, London, U.K.
Biochem J. 1987 Oct 1;247(1):101-8. doi: 10.1042/bj2470101.
The glucose-transport protein from bovine cerebral-cortex microvessels has been identified and characterized by virtue of its ability to bind the ligand [4-3H]cytochalasin B. Microvessel membranes were found to contain a single set of glucose-inhibitable high-affinity cytochalasin B-binding sites [113 +/- 16 (S.E.M.) pmol/mg of membrane protein], with an association constant of 6.8 +/- 1.8 (S.E.M.) micron-1. D-Glucose inhibited the binding to these sites with a Ki of 31 mM. The transport protein was identified by photoaffinity labelling with [4-3H]cytochalasin B and was found to migrate as a broad band of apparent Mr 55,000 on SDS/polyacrylamide gels. Labelling was inhibited by D-glucose, but not by L-glucose. Treatment with endoglycosidase F yielded a sharper band of apparent Mr 46,000, indicating that the transport protein is glycosylated. However, in contrast with the human erythrocyte glucose transporter, digestion with endo-beta-galactosidase had little effect on the electrophoretic mobility of the microvessel protein. Tryptic digestion of the photolabelled protein yielded a radioactive fragment of apparent Mr 18,000, similar to that of the fragment produced by digestion of the labelled human erythrocyte glucose transporter. In addition, a protein of Mr identical with that of the photolabelled transporter was labelled on Western blots of microvessel membranes by antisera raised against the intact erythrocyte transporter and against synthetic peptides corresponding to its N- and C-terminal regions. It is concluded that the glucose-transport protein of bovine cerebral-cortex microvessel endothelial cells shows structural homology with the human erythrocyte glucose transporter.
通过牛脑皮质微血管中葡萄糖转运蛋白结合配体[4-³H]细胞松弛素B的能力,已对其进行了鉴定和特性分析。发现微血管膜含有一组单一的葡萄糖可抑制的高亲和力细胞松弛素B结合位点[113±16(标准误)pmol/mg膜蛋白],结合常数为6.8±1.8(标准误)μmol⁻¹。D-葡萄糖以31 mM的Ki值抑制与这些位点的结合。通过用[4-³H]细胞松弛素B进行光亲和标记鉴定出转运蛋白,发现在SDS/聚丙烯酰胺凝胶上它迁移为一条表观分子量为55,000的宽带。标记受D-葡萄糖抑制,但不受L-葡萄糖抑制。用内切糖苷酶F处理产生一条表观分子量为46,000的更清晰条带,表明转运蛋白是糖基化的。然而,与人类红细胞葡萄糖转运体不同,用内切β-半乳糖苷酶消化对微血管蛋白的电泳迁移率影响很小。对光标记蛋白进行胰蛋白酶消化产生一个表观分子量为18,000的放射性片段,类似于标记的人类红细胞葡萄糖转运体消化产生的片段。此外,在微血管膜的蛋白质印迹上,与光标记转运体分子量相同的一种蛋白质被针对完整红细胞转运体及其N端和C端区域相应合成肽产生的抗血清所标记。结论是,牛脑皮质微血管内皮细胞的葡萄糖转运蛋白与人红细胞葡萄糖转运体显示出结构同源性。