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使用新型福斯可林光亲和标记物对人红细胞葡萄糖转运体进行衍生化。

Derivatization of the human erythrocyte glucose transporter using a novel forskolin photoaffinity label.

作者信息

Wadzinski B E, Shanahan M F, Ruoho A E

机构信息

Department of Pharmacology, University of Wisconsin Medical School, Madison 53706.

出版信息

J Biol Chem. 1987 Dec 25;262(36):17683-9.

PMID:3693367
Abstract

An iodinated photoaffinity label for the glucose transporter, 3-iodo-4-azidophenethylamido-7-O-succinyldeacetyl-forskolin (IAPS-forskolin), has been synthesized, purified, and characterized. The I50 for inhibition of 3-O-methylglucose transport in red blood cells by IAPS-forskolin was found to be 0.05 microM. The carrier free radioiodinated label is a highly specific photoaffinity label for the human erythrocyte glucose transporter. Photolysis of erythrocyte membranes (ghosts) and purified glucose transporter preparations with 1-2 nM [125I]IAPS-forskolin and analysis by sodium dodecyl sulfate-polyacrylamide gel electrophoresis showed specific derivatization of a broad band with an apparent molecular mass of 40-70 kDa. Photoincorporation into erythrocyte membranes using 2 nM [125I]IAPS-forskolin was protected with D-glucose (I50 400 mM), cytochalasin B (I50 0.5 microM), and forskolin (I50 10 microM). No protection was observed with L-glucose (600 mM). Endo-beta-galactosidase digestion of [125I] IAPS-forskolin-labeled ghosts and purified transporter resulted in a dramatic sharpening of the specifically radiolabeled transporter to 40 kDa. Trypsinization of [125I]IAPS-forskolin-labeled ghosts and purified transporter reduced the specifically radiolabeled transporter to a sharp peak at 18 kDa. [125I]IAPS-forskolin will be a useful tool to study the structural aspects of the glucose transporter.

摘要

一种用于葡萄糖转运蛋白的碘化光亲和标记物,即3-碘-4-叠氮苯乙酰胺基-7-O-琥珀酰去乙酰佛司可林(IAPS-佛司可林),已被合成、纯化和表征。发现IAPS-佛司可林抑制红细胞中3-O-甲基葡萄糖转运的I50为0.05微摩尔。无载体放射性碘化标记物是人类红细胞葡萄糖转运蛋白的一种高度特异性光亲和标记物。用1-2纳摩尔[125I]IAPS-佛司可林对红细胞膜(空泡)和纯化的葡萄糖转运蛋白制剂进行光解,并通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳分析,结果显示一条表观分子量为40-70 kDa的宽带发生了特异性衍生化。使用2纳摩尔[125I]IAPS-佛司可林对红细胞膜进行光掺入可被D-葡萄糖(I50 400毫摩尔)、细胞松弛素B(I50 0.5微摩尔)和佛司可林(I50 10微摩尔)保护。L-葡萄糖(600毫摩尔)未观察到保护作用。用内切β-半乳糖苷酶消化[125I]IAPS-佛司可林标记的空泡和纯化的转运蛋白,导致特异性放射性标记的转运蛋白显著锐化至分子量40 kDa。用胰蛋白酶处理[125I]IAPS-佛司可林标记的空泡和纯化的转运蛋白,使特异性放射性标记的转运蛋白减少至18 kDa的尖锐峰。[125I]IAPS-佛司可林将成为研究葡萄糖转运蛋白结构方面的有用工具。

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