RECONSTITUTION OF SOLUBILIZED ATRIAL CHOLINERGIC MUSCARINIC RECEPTORS IN LIPOSOMES

被引:7
作者
AGUILAR, JS [1 ]
OCHOA, ELM [1 ]
DEROBERTIS, E [1 ]
机构
[1] FAC MED BUENOS AIRES, INST BIOL CELULAR, RA-1121 BUENOS AIRES, DF, ARGENTINA
关键词
D O I
10.1007/BF00971369
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 > methyl-atropine > scopolamine > pirenzepine oxotremorine > gallamine > carbamylcholine > 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.
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页码:83 / 91
页数:9
相关论文
共 57 条
[2]  
AGUILAR JS, 1984, 4 BIOCH PAN C
[3]  
ARONSTAM RS, 1978, LIFE SCI, V23, P1377
[4]  
ARONSTAM RS, 1978, MOL PHARMACOL, V14, P575
[5]   GUANINE-NUCLEOTIDES MODULATE MUSCARINIC RECEPTOR-BINDING IN THE HEART [J].
BERRIE, CP ;
BIRDSALL, NJM ;
BURGEN, ASV ;
HULME, EC .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1979, 87 (04) :1000-1005
[6]  
BERRIE CP, 1986, TRENDS PHARM SCI S, V7, P8
[7]  
BIRDSALL NJM, 1978, MOL PHARMACOL, V14, P723
[8]   MUSCARINIC RECEPTOR SUBCLASSES [J].
BIRDSALL, NJM ;
HULME, EC .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1983, 4 (11) :459-463
[9]  
BROWN JH, 1984, FED PROC, V43, P2613
[10]  
BROWN JH, 1984, J BIOL CHEM, V259, P3777