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脑肽YY受体:在整个脊椎动物进化过程中的高度保守特征。

Brain peptide YY receptors: highly conserved characteristics throughout vertebrate evolution.

作者信息

Okita M, Inui A, Hirosue Y, Miura M, Nakajima M, Kasuga M

机构信息

Second Department of Internal Medicine, Kobe University School of Medicine, Japan.

出版信息

Endocrinology. 1991 Nov;129(5):2512-20. doi: 10.1210/endo-129-5-2512.

Abstract

We have shown previously that peptide YY (PYY) receptors are uniquely distributed in various mammalian brains and also have identified the receptor from porcine hippocampal membranes as a protein of 50,000 mol wt. To extend these observations, both the characteristics of PYY-receptor interaction and the structure of the receptor have been examined and compared with those of its sister peptide, neuropeptide Y (NPY), in the brains of various vertebrates including mammals (human, dog, guinea pig, rat, and mouse), birds (chicken), reptiles (snapping turtle), amphibians (bullfrog), and fish (yellowtail fish). The affinities and relative potencies of PYY as well as NPY receptors for pancreatic polypeptide (PP) family peptides were about the same in all species examined except for chickens. PYY and NPY bound to both the PYY and NPY receptors with high affinities, but porcine and avian PPs did not. In chicken brain, however, PYY, NPY, porcine PP, and avian PP all bound to the receptors with high affinity. Analysis of the equilibrium binding data for PYY receptors produced curvilinear Scatchard plots in all of the species, suggesting the existence of high and low affinity binding sites. Affinity cross-linking using disuccinimidyl suberate followed by electrophoretic analysis of ligand-receptor complexes characterized the molecular size of PYY and NPY receptors. [125I]PYY was cross-linked to a protein of 50,000 mol wt without sulfhydryl-bonded subunits on mammalian hippocampal membranes. A receptor protein with the same mol wt was identified in other brain areas, including hypothalamus and pituitary, PYY receptors in other vertebrate brains were similar in size to those of mammalian species except in chicken brain, where a receptor protein of 67,000 mol wt was observed. In addition, we also have demonstrated that the NPY receptor is a monomeric 50,000 and 55,000 mol wt protein in mammalian and fish brains, respectively. These findings indicate that brain PYY and NPY receptors in most vertebrate species from fish to man are pharmacologically and structurally similar and have been well conserved over a period of evolution of 400 million yr. The divergence of the receptors observed in chicken brain may reflect some change in their function.

摘要

我们之前已经表明,肽YY(PYY)受体在各种哺乳动物大脑中具有独特的分布,并且还从猪海马膜中鉴定出该受体是一种分子量为50,000的蛋白质。为了扩展这些观察结果,我们研究了PYY受体相互作用的特征以及受体的结构,并将其与包括哺乳动物(人类、狗、豚鼠、大鼠和小鼠)、鸟类(鸡)、爬行动物(鳄龟)、两栖动物(牛蛙)和鱼类(黄尾鱼)在内的各种脊椎动物大脑中的姐妹肽神经肽Y(NPY)进行了比较。除鸡外,在所有检测的物种中,PYY以及NPY受体对胰多肽(PP)家族肽的亲和力和相对效力大致相同。PYY和NPY以高亲和力与PYY和NPY受体结合,但猪和禽PP则不结合。然而,在鸡脑中,PYY、NPY、猪PP和禽PP都以高亲和力与受体结合。对PYY受体的平衡结合数据进行分析,在所有物种中均产生曲线型Scatchard图,表明存在高亲和力和低亲和力结合位点。使用辛二酸二琥珀酰亚胺酯进行亲和交联,随后对配体 - 受体复合物进行电泳分析,确定了PYY和NPY受体的分子大小。[125I]PYY在哺乳动物海马膜上与一种分子量为50,000且无巯基结合亚基的蛋白质交联。在包括下丘脑和垂体在内的其他脑区也鉴定出了具有相同分子量的受体蛋白。除鸡脑外,其他脊椎动物脑中的PYY受体大小与哺乳动物物种相似,在鸡脑中观察到一种分子量为67,000的受体蛋白。此外,我们还证明,在哺乳动物和鱼类大脑中,NPY受体分别是分子量为50,000和55,000的单体蛋白。这些发现表明,从鱼类到人类的大多数脊椎动物物种的脑PYY和NPY受体在药理学和结构上相似,并且在4亿年的进化过程中得到了很好的保守。在鸡脑中观察到的受体差异可能反映了其功能的某些变化。

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