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四氢蝶呤干扰盘基网柄菌中的G蛋白信号通路。

Tetrahydropterins interfere with the G protein pathway in Dictyostelium discoideum.

作者信息

Ziegler I, Gütlich M

机构信息

GSF-Institut für Klinische Molekularbiologie und Tumorgenetik, München, Germany.

出版信息

Biochem Biophys Res Commun. 1996 Apr 16;221(2):368-73. doi: 10.1006/bbrc.1996.0602.

Abstract

The cellular slime mold Dictyostelium discoideum produces tetrahydrodictyopterin, the D-threo-isomer of tetrahydrobiopterin. During cyclic AMP coordinated aggregation, the G protein linked signalling pathway is involved in the regulation of the initial enzyme GTP cyclohydrolase I [M. Gütlich et al., Biochem. J. 314, 95-101 (1996)]. We now find that cyclic AMP stimulated binding of GTPgammaS to the membrane fraction is inhibited by tetrahydrodictyopterin and tetrahydrobiopterin. Inhibition was a function of GTPgammaS concentration and the analysis of the kinetic data pointed to a competitive type of inhibition. The inhibition of G protein activation was accompanied by a loss of adenylyl cyclase activation. Because the GTPgammaS- and G protein-dependent reduction of receptor affinity for cyclic AMP was also attenuated, we conclude that tetrahydrodictyopterin and tetrahydrobiopterin interfere with activation of G proteins by inhibiting GDP-GTP exchange.

摘要

细胞黏菌盘基网柄菌能产生四氢蝶啶,即四氢生物蝶呤的D-苏式异构体。在环磷酸腺苷(cAMP)协调的聚集过程中,G蛋白偶联信号通路参与了初始酶GTP环化水解酶I的调节[M. Gütlich等人,《生物化学杂志》314, 95 - 101 (1996)]。我们现在发现,四氢蝶啶和四氢生物蝶呤可抑制cAMP刺激的GTPγS与膜组分的结合。抑制作用是GTPγS浓度的函数,动力学数据分析表明这是一种竞争性抑制类型。G蛋白激活的抑制伴随着腺苷酸环化酶激活的丧失。由于GTPγS和G蛋白依赖的受体对cAMP亲和力的降低也被减弱,我们得出结论,四氢蝶啶和四氢生物蝶呤通过抑制GDP - GTP交换来干扰G蛋白的激活。

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