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1
Target size of the adenosine Ri receptor.腺苷 Ri 受体的靶标大小。
Biochem J. 1986 Apr 15;235(2):621-4. doi: 10.1042/bj2350621.
2
Hydrodynamic properties of adenosine Ri receptors solubilized from rat cerebral-cortical membranes.从大鼠大脑皮层膜中溶解出的腺苷 Ri 受体的流体动力学特性。
Biochem J. 1987 Dec 15;248(3):635-42. doi: 10.1042/bj2480635.
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Two affinity states of Ri adenosine receptors in brain membranes. Analysis of guanine nucleotide and temperature effects on radioligand binding.脑膜中Ri腺苷受体的两种亲和状态。鸟嘌呤核苷酸和温度对放射性配体结合影响的分析。
Mol Pharmacol. 1984 Jul;26(1):1-9.
4
Magnesium ion exerts a central role in the regulation of inhibitory adenosine receptors.镁离子在抑制性腺苷受体的调节中发挥核心作用。
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Chronic caffeine ingestion sensitizes the A1 adenosine receptor-adenylate cyclase system in rat cerebral cortex.长期摄入咖啡因会使大鼠大脑皮层中的A1腺苷受体-腺苷酸环化酶系统敏感化。
J Clin Invest. 1986 Jan;77(1):222-7. doi: 10.1172/JCI112280.
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Guanine nucleotide sensitivity of [125I]-Iodo NTyr somatostatin binding in rat adenohypophysis and cerebral cortex.大鼠腺垂体和大脑皮质中[125I]-碘酪氨生长抑素结合的鸟嘌呤核苷酸敏感性
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Solubilization of A1 adenosine receptor from pig brain: characterization and evidence of the role of the cell membrane on the coexistence of high- and low-affinity states.
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Phosphorylated adenosine derivatives as low-affinity adenosine-receptor agonists. Methodological implications for the adenylate cyclase assay.磷酸化腺苷衍生物作为低亲和力腺苷受体激动剂。腺苷酸环化酶测定的方法学意义。
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Evidence for an A2-like adenosine receptor on cerebral cortical neurons.大脑皮质神经元上存在A2样腺苷受体的证据。
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Distinctions in beta-adrenergic receptor interactions with the magnesium-guanine nucleotide coupling proteins in turkey erythrocyte and S49 lymphoma membranes.火鸡红细胞和S49淋巴瘤细胞膜中β-肾上腺素能受体与镁-鸟嘌呤核苷酸偶联蛋白相互作用的差异。
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2
Heteromeric association creates a P2Y-like adenosine receptor.异源缔合产生一种P2Y样腺苷受体。
Proc Natl Acad Sci U S A. 2001 Jun 19;98(13):7617-22. doi: 10.1073/pnas.121587098. Epub 2001 Jun 5.
3
Hydrodynamic properties of adenosine Ri receptors solubilized from rat cerebral-cortical membranes.从大鼠大脑皮层膜中溶解出的腺苷 Ri 受体的流体动力学特性。
Biochem J. 1987 Dec 15;248(3):635-42. doi: 10.1042/bj2480635.

本文引用的文献

1
Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
J Biol Chem. 1951 Nov;193(1):265-75.
2
Size determination of an equilibrium enzymic system by radiation inactivation: theoretical considerations.通过辐射失活法测定平衡酶系统的大小:理论思考
Biochem J. 1982 Sep 1;205(3):477-83. doi: 10.1042/bj2050477.
3
Size of acetylcholine receptors in the membrane. An improved version of the radiation inactivation method.膜中乙酰胆碱受体的大小。辐射失活法的改进版本。
Biochemistry. 1982 Apr 27;21(9):2210-7. doi: 10.1021/bi00538a033.
4
Muscarinic cholinergic receptor structure. Receptor size, membrane orientation, and absence of major phylogenetic structural diversity.毒蕈碱型胆碱能受体结构。受体大小、膜取向以及主要系统发育结构多样性的缺失。
J Biol Chem. 1983 Apr 25;258(8):4842-8.
5
Simulation of an inhibitory equilibrium system. Aberrant proteinic target sizes as obtained by radiation inactivation.抑制性平衡系统的模拟。通过辐射失活获得的异常蛋白质靶标大小。
Biochem J. 1984 Aug 15;222(1):273-6. doi: 10.1042/bj2220273.
6
[3H]5'-N-ethylcarboxamide adenosine binds to both Ra and Ri adenosine receptors in rat striatum.[3H]5'-N-乙基羧酰胺腺苷与大鼠纹状体中的Ra和Ri腺苷受体均有结合。
Naunyn Schmiedebergs Arch Pharmacol. 1984 Mar;325(3):218-25. doi: 10.1007/BF00495947.
7
Molecular properties of the slow inward calcium channel. Molecular weight determinations by radiation inactivation and covalent affinity labeling.
J Biol Chem. 1983 Aug 10;258(15):9344-8.
8
Agonist and antagonist affinities for inhibitory adenosine receptors are reciprocally affected by 5'-guanylylimidodiphosphate or N-ethylmaleimide.激动剂和拮抗剂对抑制性腺苷受体的亲和力会受到5'-鸟苷酰亚胺二磷酸或N-乙基马来酰亚胺的相互影响。
J Biol Chem. 1983 Feb 25;258(4):2334-9.
9
Adenosine receptors in fat cells. Identification by (-)-N6-[3H]phenylisopropyladenosine binding.脂肪细胞中的腺苷受体。通过(-)-N6-[3H]苯异丙基腺苷结合进行鉴定。
Mol Pharmacol. 1981 Mar;19(2):228-35.
10
Ligand: a versatile computerized approach for characterization of ligand-binding systems.配体:一种用于表征配体结合系统的通用计算机化方法。
Anal Biochem. 1980 Sep 1;107(1):220-39. doi: 10.1016/0003-2697(80)90515-1.

腺苷 Ri 受体的靶标大小。

Target size of the adenosine Ri receptor.

作者信息

Frame L T, Yeung S M, Venter J C, Cooper D M

出版信息

Biochem J. 1986 Apr 15;235(2):621-4. doi: 10.1042/bj2350621.

DOI:10.1042/bj2350621
PMID:3017310
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1146730/
Abstract

The adenosine receptor of rat cerebral-cortical membranes was examined by radiation inactivation. In control membranes the receptor is distributed between high- and low-affinity states, that can be preferentially expressed by Mg2+ ions and guanine nucleotides respectively. Upon exposure to increasing doses of radiation, the high-affinity receptor decayed linearly as a function of radiation dose. This decay rate corresponded to a target size of 63,000 Da, when compared with the decay of the muscarinic cholinergic receptor that was also measured in these membranes.

摘要

通过辐射失活法检测大鼠大脑皮层膜中的腺苷受体。在对照膜中,该受体分布于高亲和力和低亲和力状态之间,分别可由Mg2+离子和鸟嘌呤核苷酸优先表达。随着辐射剂量增加,高亲和力受体随辐射剂量呈线性衰减。与同样在这些膜中测量的毒蕈碱型胆碱能受体的衰减相比,这种衰减速率对应于63,000 Da的靶标大小。