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脂质体中溶解的心房胆碱能毒蕈碱受体的重组。

Reconstitution of solubilized atrial cholinergic muscarinic receptors in liposomes.

作者信息

Aguilar J S, Ochoa E L, De Robertis E

出版信息

Neurochem Res. 1987 Jan;12(1):83-91. doi: 10.1007/BF00971369.

Abstract

The reconstitution of solubilized bovine atrial cholinergic muscarinic receptor into liposomes made of exogenous lipids has been achieved by polyethyleneglycol precipitation. Of the different lipid mixtures used, soybean lecithins were shown to be the best on the basis of receptor recovery. The receptor reconstituted into soybean lecithins liposomes exhibited ligand binding properties very similar to those of the native receptor. The dissociation constant of [3H]-N-methyl-scopolamine ([3H]NMS) was 0.46 and 0.30 nM as determined by equilibrium and kinetics experiments respectively. The potency of a range of muscarinic ligands in displacing [3H]NMS binding was atropine greater than methyl-atropine greater than scopolamine greater than pirenzepine oxotremorine greater than gallamine greater than carbamylcholine greater than pilocarpine bethanechol. The Hill slopes of the displacement curves were near 1 for the antagonists and smaller than 1 for the agonists and for gallamine. The agonist binding may be modulated by guanine nucleotides. These results indicate that soybean lecithins fulfill the lipid requirements for the reconstitution of the atrial muscarinic receptor.

摘要

通过聚乙二醇沉淀法已成功将溶解的牛心房胆碱能毒蕈碱受体重组成由外源性脂质制成的脂质体。在所使用的不同脂质混合物中,基于受体回收率,大豆卵磷脂被证明是最佳的。重组成大豆卵磷脂脂质体的受体表现出与天然受体非常相似的配体结合特性。通过平衡实验和动力学实验分别测定,[³H]-N-甲基东莨菪碱([³H]NMS)的解离常数为0.46和0.30 nM。一系列毒蕈碱配体置换[³H]NMS结合的效力顺序为:阿托品>甲基阿托品>东莨菪碱>哌仑西平>氧化震颤素>加拉明>氨甲酰胆碱>毛果芸香碱>氨甲酰甲胆碱。拮抗剂置换曲线的希尔斜率接近1,激动剂和加拉明的置换曲线希尔斜率小于1。激动剂结合可能受鸟嘌呤核苷酸调节。这些结果表明,大豆卵磷脂满足心房毒蕈碱受体重组的脂质要求。

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