Suppr超能文献

GTP结合蛋白Go在脊椎动物和无脊椎动物不同组织中的免疫定位。

Immunological localization of the GTP-binding protein Go in different tissues of vertebrates and invertebrates.

作者信息

Homburger V, Brabet P, Audigier Y, Pantaloni C, Bockaert J, Rouot B

出版信息

Mol Pharmacol. 1987 Apr;31(4):313-9.

PMID:3106786
Abstract

Bovine brain contains two GTP-binding proteins, Gi and Go, which are substrates for ADP ribosylation by pertussis toxin. The Gi protein mediates hormone and GTP inhibition of adenylate cyclase, but the function and the precise tissue distribution of Go are unknown. To immunologically probe the localization of Go, we have purified the Go alpha and G beta, gamma subunits of Go and have raised antibodies against them. The polyclonal anti-Go alpha antibodies obtained were very selective for Go alpha compared to Gi alpha or Gs alpha. The positive Go alpha and G beta, gamma immunoreactivities were investigated in different tissues of vertebrates and invertebrates on immunoblots after gel electrophoresis of the crude membranes. The anti-G beta, gamma antibodies recognized a 35-36-kDa protein in brain of vertebrates such as mammals (rat), avians (pigeon), amphibians (frog), fish (trout), and reptiles (turtle) but not in the invertebrates such as molluscs (snail) and insects (locust). With the anti-Go alpha antibodies a high level of immunoreactivity was detected at molecular weights of 39,000-40,000 in the brain of invertebrates as well as in the central nervous system of vertebrates. Moreover, ADP ribosylation with pertussis toxin occurred in the nervous system of invertebrates. These results suggest that the GTP-binding proteins of invertebrates either are devoid of G beta, gamma subunit or, more probably, possess immunologically different G beta, gamma subunits when compared to those of vertebrates. In the vertebrates, Go alpha immunoreactivity was also present in the peripheral nervous system in areas such as the superior cervical ganglia and sciatic nerve. When examined with the anti-Go alpha antibodies, the neuro-and adenohypophysis exhibited a similar immunoreactivity which was about 6 times lower than in brain. Our antibodies also recognized a 40-kDa protein in human adipocytes but at a concentration 17 times lower than that recognized in brain. Taken together, these data show that the Go alpha subunit is well conserved through evolution and, furthermore, confirm that Go alpha is not strictly limited to the nervous system. This suggests that the protein Go ensures a function required for neuronal activity but also present in some other non-nervous tissues.

摘要

牛脑含有两种GTP结合蛋白,Gi和Go,它们是百日咳毒素进行ADP核糖基化的底物。Gi蛋白介导激素和GTP对腺苷酸环化酶的抑制作用,但Go的功能和确切组织分布尚不清楚。为了通过免疫方法探究Go的定位,我们纯化了Go的α亚基和Gβγ亚基,并制备了针对它们的抗体。与Giα或Gsα相比,所获得的多克隆抗Goα抗体对Goα具有高度选择性。在对粗制膜进行凝胶电泳后,通过免疫印迹法研究了脊椎动物和无脊椎动物不同组织中Goα和Gβγ的阳性免疫反应性。抗Gβγ抗体在哺乳动物(大鼠)、鸟类(鸽子)、两栖动物(青蛙)、鱼类(鳟鱼)和爬行动物(乌龟)等脊椎动物的脑中识别出一种35 - 36 kDa的蛋白质,但在软体动物(蜗牛)和昆虫(蝗虫)等无脊椎动物中未识别出。使用抗Goα抗体,在无脊椎动物的脑中以及脊椎动物的中枢神经系统中,在分子量为39,000 - 40,000处检测到高水平的免疫反应性。此外,百日咳毒素对无脊椎动物的神经系统进行了ADP核糖基化。这些结果表明,无脊椎动物的GTP结合蛋白要么缺乏Gβγ亚基,要么更可能与脊椎动物的Gβγ亚基在免疫上不同。在脊椎动物中,Goα免疫反应性也存在于外周神经系统的某些区域,如颈上神经节和坐骨神经。用抗Goα抗体检测时,神经垂体和腺垂体表现出相似的免疫反应性,其强度比脑中低约6倍。我们的抗体还在人脂肪细胞中识别出一种40 kDa的蛋白质,但其浓度比在脑中识别出的浓度低17倍。综上所述,这些数据表明Goα亚基在进化过程中高度保守,此外,证实Goα并不严格局限于神经系统。这表明Go蛋白确保了神经元活动所需的一种功能,并且也存在于一些其他非神经组织中。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验