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来自大鼠肝脏的胰岛素和胰高血糖素刺激的“致密囊泡”高亲和力环磷酸腺苷磷酸二酯酶。纯化、特性鉴定及抑制剂敏感性

The insulin- and glucagon-stimulated 'dense-vesicle' high-affinity cyclic AMP phosphodiesterase from rat liver. Purification, characterization and inhibitor sensitivity.

作者信息

Pyne N J, Cooper M E, Houslay M D

出版信息

Biochem J. 1987 Feb 15;242(1):33-42. doi: 10.1042/bj2420033.

Abstract

The hormone-stimulated 'dense-vesicle' cyclic AMP phosphodiesterase was solubilized as a proteolytically 'clipped' species, and purified to apparent homogeneity from rat liver with a 2000-3000-fold purification and a 13-18% yield. It appeared to be a dimer (Mr 112,000), of two Mr-57,000 subunits. Solubilization of either a liver or a hepatocyte membrane fraction, with sodium cholate in the presence of the protein inhibitor benzamidine, identified three protein bands which could be immunoprecipitated by a polyclonal antibody raised against the pure enzyme. The major band at Mr 62,000 is suggested to be the native 'dense-vesicle' enzyme, having a Mr-5000 extension which serves to anchor this enzyme to the membrane and which is cleaved off during proteolytic solubilization; the Mr-200,000 band is an aggregate of the Mr-62,000 species, and the Mr-63,000 species is possibly a precursor. The purified 'clipped' enzyme hydrolysed cyclic AMP with kinetics indicative of apparent negative co-operativity, with a Hill coefficient (h) of 0.43 and limiting kinetic constants of Km1 = 0.3 +/- 0.05 microM, Km2 = 29 +/- 6 microM, Vmax.1 = 0.114 +/- 0.015 unit/mg of protein and Vmax.2 = 0.633 +/- 0.054 unit/mg of protein. It hydrolysed cyclic GMP with Michaelis kinetics, Km = 10 +/- 1 microM and Vmax. = 4.1 +/- 0.2 units/mg of protein. Cyclic GMP was a potent inhibitor of cyclic AMP hydrolysis, with an IC50 (concn. giving 50% inhibition) of 0.20 +/- 0.01 microM-cyclic GMP when assayed at 0.1 microM-cyclic AMP. This enzyme was inhibited potently by several drugs known to exert positive inotropic effects on the heart, was extremely thermolabile, with a half-life of 4.5 +/- 0.5 min at 40 degrees C, and was shown to be distinct from the rat liver insulin-stimulated peripheral-plasma-membrane cyclic AMP phosphodiesterase [Marchmont, Ayad & Houslay (1981) Biochem. J. 195, 645-652].

摘要

激素刺激的“致密囊泡”环磷酸腺苷磷酸二酯酶以蛋白水解“剪切”形式溶解,并从大鼠肝脏中纯化至表观均一,纯化倍数为2000 - 3000倍,产率为13 - 18%。它似乎是一个二聚体(Mr 112,000),由两个Mr - 57,000亚基组成。在蛋白质抑制剂苯甲脒存在下,用胆酸钠溶解肝脏或肝细胞膜部分,鉴定出三条可被针对纯酶产生的多克隆抗体免疫沉淀的蛋白带。Mr 62,000处的主要条带被认为是天然的“致密囊泡”酶,具有一个Mr - 5000的延伸部分,用于将该酶锚定在膜上,在蛋白水解溶解过程中被切割掉;Mr - 200,000条带是Mr - 62,000物种的聚集体,Mr - 63,000物种可能是前体。纯化的“剪切”酶水解环磷酸腺苷,动力学表现出明显的负协同性,希尔系数(h)为0.43,极限动力学常数为Km1 = 0.3 ± 0.05 microM,Km2 = 29 ± 6 microM,Vmax.1 = 0.114 ± 0.015单位/毫克蛋白,Vmax.2 = 0.633 ± 0.054单位/毫克蛋白。它以米氏动力学水解环磷酸鸟苷,Km = 10 ± 1 microM,Vmax. = 4.1 ± 0.2单位/毫克蛋白。环磷酸鸟苷是环磷酸腺苷水解的有效抑制剂,在0.1 microM环磷酸腺苷测定时,IC50(产生50%抑制的浓度)为0.20 ± 0.01 microM环磷酸鸟苷。该酶被几种已知对心脏有正性肌力作用的药物强烈抑制,极不耐热,在40℃下半衰期为4.5 ± 0.5分钟,并且被证明与大鼠肝脏胰岛素刺激的外周质膜环磷酸腺苷磷酸二酯酶不同[Marchmont,Ayad & Houslay(1981)Biochem. J. 195,645 - 652]。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/141f/1147660/7d639755974e/biochemj00261-0047-a.jpg

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