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使用5-氨基依酚氯铵作为配体从大鼠脑中亲和分离咪唑啉结合蛋白。

Affinity isolation of imidazoline binding proteins from rat brain using 5-amino-efaroxan as a ligand.

作者信息

Monks L K, Cosgrove K E, Dunne M J, Ramsden C A, Morgan N G, Chan S L

机构信息

Cellular Pharmacology Group, School of Life Sciences, Keele University, Staffordshire, UK.

出版信息

FEBS Lett. 1999 Mar 19;447(1):61-4. doi: 10.1016/s0014-5793(99)00264-1.

Abstract

We have employed an amino derivative of the imidazoline ligand, efaroxan, to isolate imidazoline binding proteins from solubilised extracts of rat brain, by affinity chromatography. A number of proteins were specifically retained on the affinity column and one of these was immunoreactive with an antiserum raised against the ion conducting pore component of the ATP-sensitive potassium channel. Patch clamp experiments confirmed that, like its parent compound, amino-efaroxan blocks ATP-sensitive potassium channels in human pancreatic beta-cells and can stimulate the insulin secretion from these cells. The results reveal that a member of the ion conducting pore component family is strongly associated with imidazoline binding proteins in brain and in the endocrine pancreas.

摘要

我们已使用咪唑啉配体的氨基衍生物依酚氯铵,通过亲和色谱法从大鼠脑的可溶性提取物中分离咪唑啉结合蛋白。一些蛋白质特异性地保留在亲和柱上,其中一种与针对ATP敏感性钾通道的离子传导孔成分产生的抗血清发生免疫反应。膜片钳实验证实,氨基依酚氯铵与其母体化合物一样,可阻断人胰岛β细胞中的ATP敏感性钾通道,并能刺激这些细胞分泌胰岛素。结果表明,离子传导孔成分家族的一个成员与脑和内分泌胰腺中的咪唑啉结合蛋白密切相关。

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