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大鼠肝脏血管加压素(V1)受体的纯化与特性分析。

Purification and characterization of the rat liver vasopressin (V1) receptor.

作者信息

Fishman J B, Dickey B F, Fine R E

机构信息

Department of Biochemistry, Boston University Medical School, Massachusetts.

出版信息

J Biol Chem. 1987 Oct 15;262(29):14049-55.

PMID:2958456
Abstract

Utilizing a proteoliposome reconstitution system, we have purified the rat liver V1 vasopressin receptor to near homogeneity. The receptor was purified approximately 21,000-fold from rat liver membranes, using differential detergent solubilization, size exclusion gel filtration, lectin affinity, and ion-exchange chromatography. The purified receptor exhibits a Kd of 6 nM, when, prior to solubilization, the membranes were exposed to 1 microM vasopressin. This resulted in the association of a pertussis toxin-insensitive guanine nucleotide-binding protein with the receptor during most of the purification procedure. In the absence of this association, the receptor had a Kd of approximately 30 nM. Association of the receptor with a G-protein was confirmed by the ability of vasopressin to stimulate the hydrolysis of [gamma-32P]GTP. The specific activity of the vasopressin-stimulated hydrolysis was 25 nmol/min/mg, approximately 8,000-fold higher than values obtained with crude reconstituted receptor preparations. Cross-linking of 125I-vasopressin to a partially purified preparation of receptor demonstrated that the receptor had a molecular weight of approximately 68,000 under reducing conditions, and 58,000 under nonreducing conditions. The purification procedure may prove useful in purifying a number of small peptide hormone receptors (e.g. bradykinin, angiotensin II) and perhaps their associated G-proteins as well.

摘要

利用蛋白脂质体重组系统,我们已将大鼠肝脏V1血管加压素受体纯化至接近均一的状态。通过差示去污剂增溶、尺寸排阻凝胶过滤、凝集素亲和层析和离子交换层析,该受体从大鼠肝膜中纯化了约21,000倍。当在增溶前将膜暴露于1 μM血管加压素时,纯化后的受体表现出6 nM的解离常数(Kd)。这导致在大部分纯化过程中,一种对百日咳毒素不敏感的鸟嘌呤核苷酸结合蛋白与受体结合。在没有这种结合的情况下,受体的Kd约为30 nM。血管加压素刺激[γ-32P]GTP水解的能力证实了受体与G蛋白的结合。血管加压素刺激水解的比活性为25 nmol/min/mg,比用粗制重组受体制剂获得的值高约8,000倍。将125I-血管加压素与部分纯化的受体制剂交联表明,该受体在还原条件下的分子量约为68,000,在非还原条件下为58,000。该纯化程序可能有助于纯化多种小肽激素受体(如缓激肽、血管紧张素II),或许还能纯化它们相关的G蛋白。

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