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可溶性β-肾上腺素能受体在细胞膜中的功能性植入。

Functional implantation of a solubilized beta-adrenergic receptor in the membrane of a cell.

作者信息

Eimerl S, Neufeld G, Korner M, Schramm M

出版信息

Proc Natl Acad Sci U S A. 1980 Feb;77(2):760-4. doi: 10.1073/pnas.77.2.760.

Abstract

When the beta-adrenergic receptor of turkey erythrocytes was solubilized by deoxycholate, it retained its potential to activate an adenylate cyclase system. Electron microscopy showed that true solubilization had apparently been achieved; no residual membrane or vesicle structure was found. After removal of deoxycholate and addition of phospholipid, the reprecipitated beta-adrenergic receptor was implanted in the cell membrane of Friend erythroleukemia cells by using a chemical fusion method recently developed. Membranes prepared from the cells demonstrated 30-fold stimulation of the Friend cell adenylate cyclase by the implanted beta-adrenergic receptor. The function of the indigenous prostaglandin E(1) receptor of the Friend cells was not much affected by the implantation of large amounts of the foreign receptor. Activity mediated by the beta-adrenergic receptor reached 60% of the activity obtained with fluoride. The implanted receptor is therefore considered to be efficiently coupled to the adenylate cyclase system. The major difficulties hitherto preventing solubilization of hormone receptors and subsequent reconstitution of their function have been overcome by the approach developed in the present work. Conditions of solubilization need preserve only the receptor because all other components, even those unidentified as yet, can be supplied in excess by the adenylate cyclase system of the cell in which the receptor will be implanted. Subsequent recoupling of the receptor to the adenylate cyclase is performed in the native insoluble state of these molecules. Thus, the components need not be subjected to the hazards of solubilization in a common detergent as is usually required in reconstitution procedures. The importance of using implantation as an assay for a functional receptor in the course of purification and the likelihood that the procedure can be adapted to other receptors for hormones and neurotransmitters are discussed.

摘要

当火鸡红细胞的β-肾上腺素能受体用脱氧胆酸盐增溶时,它保留了激活腺苷酸环化酶系统的能力。电子显微镜显示显然已实现了真正的增溶;未发现残留的膜或囊泡结构。去除脱氧胆酸盐并添加磷脂后,通过最近开发的化学融合方法将再沉淀的β-肾上腺素能受体植入弗瑞德红白血病细胞的细胞膜中。用植入的β-肾上腺素能受体制备的细胞膜对弗瑞德细胞腺苷酸环化酶的刺激作用提高了30倍。大量植入外源受体对弗瑞德细胞自身前列腺素E(1)受体的功能影响不大。由β-肾上腺素能受体介导的活性达到用氟化物获得的活性的60%。因此,植入的受体被认为能有效地与腺苷酸环化酶系统偶联。目前这项工作所采用的方法克服了迄今为止阻碍激素受体增溶及其功能重建的主要困难。增溶条件只需保留受体,因为所有其他成分,即使是那些尚未明确的成分,都可以由将要植入受体的细胞的腺苷酸环化酶系统过量提供。随后受体与腺苷酸环化酶的重新偶联是在这些分子的天然不溶状态下进行的。因此,这些成分不必像重建程序通常要求的那样经受在普通去污剂中增溶的风险。文中讨论了在纯化过程中使用植入法作为功能性受体检测方法的重要性,以及该程序适用于其他激素和神经递质受体的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7116/348360/d297bfec4515/pnas00665-0076-a.jpg

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