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未偶联的S49淋巴瘤刺激性GTP结合蛋白中病变的鉴定。

Identification of the lesion in the stimulatory GTP-binding protein of the uncoupled S49 lymphoma.

作者信息

Rall T, Harris B A

机构信息

Merrell Dow Research Institute, Strasbourg, France.

出版信息

FEBS Lett. 1987 Nov 30;224(2):365-71. doi: 10.1016/0014-5793(87)80486-6.

Abstract

The stimulatory GTP-binding protein (Gs) of the uncoupled mutant of S49 lymphoma cells is deficient in its ability to transduce hormonal signals from ligand-bound beta-adrenergic receptors to the catalytic component of adenylate cyclase. In order to define the genetic defect in the Gs of uncoupled S49 cells, a complementary DNA clone encoding the alpha-subunit of Gs was analyzed and the deduced primary structure of the defective subunit compared to that of the wild-type subunit. A single nucleotide transversion was found that coded for a proline rather than an arginine at residue 389. The results indicate a domain of the alpha-subunit of Gs that specifically interacts with hormone receptors.

摘要

S49淋巴瘤细胞解偶联突变体的刺激性GTP结合蛋白(Gs)在将激素信号从配体结合的β-肾上腺素能受体转导至腺苷酸环化酶催化成分的能力方面存在缺陷。为了确定解偶联S49细胞Gs中的基因缺陷,分析了编码Gsα亚基的互补DNA克隆,并将缺陷亚基的推导一级结构与野生型亚基进行比较。发现一个单核苷酸颠换,该颠换在第389位残基处编码脯氨酸而非精氨酸。结果表明Gsα亚基存在一个与激素受体特异性相互作用的结构域。

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