首页> 美国卫生研究院文献>Biochemical Journal >Photoaffinity-labelling of the calcium-channel-associated 14-dihydropyridine and phenylalkylamine receptor in guinea-pig hippocampus. A 195 kDa polypeptide carries both drug receptors and has similarities to the alpha 1 subunit of the purified skeletal-muscle calcium channel.
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Photoaffinity-labelling of the calcium-channel-associated 14-dihydropyridine and phenylalkylamine receptor in guinea-pig hippocampus. A 195 kDa polypeptide carries both drug receptors and has similarities to the alpha 1 subunit of the purified skeletal-muscle calcium channel.

机译:豚鼠海马中钙通道相关的14-二氢吡啶和苯烷基胺受体的光亲和标记。 195 kDa多肽带有两种药物受体与纯化的骨骼肌钙通道的alpha 1亚基相似。

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摘要

This study identifies calcium-antagonist-receptor-carrying polypeptides of calcium channels in guinea-pig hippocampus membranes. The arylazide ligands (-)-[3H]azidopine and [N-methyl-3H]LU49888 [(-)-5-[(3-azidophenethyl) [N-methyl-3H]methylamino]-2-(3,4,5-trimethoxyphenyl-2- isopropylvaleronitrile] were used to selectively label 1,4-dihydropyridine and phenylalkylamine receptors respectively. In the absence of u.v. light, both ligands reversibly bound to a single class of high-affinity receptors with a calcium-channel-typical pharmacological profile. [N-methyl-3H]LU49888 bound to the extent of 849 +/- 188 fmol/mg of protein (mean +/- S.D., n = 3) with a dissociation constant (Kd) of 1.4 +/- 0.3 nM. Under identical assay conditions (-)-[3H]azidopine labelled to the extent of 562 +/- 132 fmol/mg of protein with a Kd of 0.096 +/- 0.024 nM. After u.v. irradiation of the [N-methyl-3H]LU49888- and (-)-[3H]azidopine-labelled membranes, both photo-affinity probes were found to be incorporated specifically into a 190-195 kDa band as shown by SDS/polyacrylamide-gel electrophoresis (SDS/PAGE). Photoincorporation occurred with a protection profile identical with that produced by reversible binding-inhibition. [N-methyl-3H]LU49888, but not (-)-[3H]-azidopine, specifically labelled an additional 265 kDa band. Both photolabelled bands had an identical electrophoretic mobility on SDS/PAGE, irrespective of pretreatment either with 10 mM-N-ethylmaleimide or 10 mM-dithiothreitol. The electrophoretic properties of the 195 kDa polypeptide and the lability of receptor-incorporated (-)-[3H]azidopine to nucleophilic agents resemble those of the previously described drug-receptor-carrying alpha 1 subunit of the purified skeletal-muscle calcium channel. The data suggest that this polypeptide carries both the high-affinity 1,4-dihydropyridine as well as the phenylalkylamine receptor of neuronal calcium channels in guinea-pig hippocampus and is a component of the L-type calcium channel.
机译:这项研究确定了豚鼠海马膜中钙通道的携带钙拮抗剂受体的多肽。芳基叠氮化物配体(-)-[3H]叠氮平和[N-甲基-3H] LU49888 [(-)-5-[(3-叠氮苯乙基)[N-甲基-3H]甲基氨基] -2-(3,4, [5-三甲氧基苯基-2-异丙基戊腈]分别用于选择性标记1,4-二氢吡啶和苯基烷基胺受体,在不存在紫外线的情况下,两个配体可逆地结合到一类具有钙通道类型的高亲和力受体上[N-甲基-3H] LU49888结合至849 +/- 188 fmol / mg蛋白质(平均+/- SD,n = 3)的程度,解离常数(Kd)为1.4 +/- 0.3 nM。在相同的测定条件下,(-)-[3H]叠氮平标记的蛋白质程度为562 +/- 132 fmol / mg蛋白质,Kd为0.096 +/- 0.024 nM。在[N-甲基-发现3H] LU49888-和(-)-[3H]叠氮平标记的膜,如SDS /聚丙烯酰胺凝胶电泳(SDS / PAGE)所示,两个光亲和探针均被特异性结合到190-195 kDa带中。发生光掺入保护特性与可逆结合抑制所产生的保护特性相同。 [N-甲基-3H] LU49888,但未标记(-)-[3H]-叠氮平,专门标记了另外一个265 kDa带。不论用10 mM-N-乙基马来酰亚胺或10 mM-二硫苏糖醇进行预处理,两个光标记带在SDS / PAGE上均具有相同的电泳迁移率。 195 kDa多肽的电泳特性和掺入受体的(-)-[3H]叠氮平对亲核试剂的不稳定性类似于先前描述的纯化的骨骼肌钙通道的携带药物受体的α1亚基。数据表明,该多肽在豚鼠海马中携带高亲和力的1,4-二氢吡啶以及神经元钙通道的苯烷基胺受体,并且是L型钙通道的组成部分。

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