Ciuffo G M, Heemskerk F M, Saavedra J M
Section on Pharmacology, National Institute of Mental Health, National Institutes of Health, Bethesda, MD 20892.
Proc Natl Acad Sci U S A. 1993 Dec 1;90(23):11009-13. doi: 10.1073/pnas.90.23.11009.
Angiotensin II (Ang II) AT2 receptors were purified 40,000-fold to a nearly homogeneous state after solubilization from neonatal rat kidney membranes with 3-[(3-cholamidopropyl)dimethylammonio]-2-hydroxy-1-propane-sulfonic acid. Comparable IC50 values for the soluble extract (0.32 nM) and membranes (0.31 nM) were obtained by competition curves with 125I-labeled CGP42112, a selective AT2 ligand. Binding to AT2 receptors in the soluble extract was not sensitive to dithiothreitol. AT2 receptors were further purified by gel filtration and a CGP42112 Sepharose affinity column. Ang II AT2 receptors were selectively eluted with 5 microM CGP42112 at 4 degrees C, and a single band with an apparent molecular mass of 71 kDa was obtained after SDS/PAGE. Two-dimensional electrophoresis confirmed the purity of the protein and an isoelectric point of 5.3-5.5 was obtained. A highly selective elution of the AT2 receptors from the affinity column was performed with 5 nM 125I-labeled CGP42112 at room temperature after the column was treated with 1 microM losartan in the presence of high salt. After cross-linking, a major labeled protein with similar molecular mass and isoelectric point was obtained. Dissociation of the radiolabeled protein was insensitive to losartan but was enhanced by CGP42112, PD123177, Ang II, and [Sar1]Ang II. In summary, Ang II AT2 receptors were purified by CGP42112 affinity chromatography and selective elution and retain the pharmacological specificity of particulate receptors.
用3-[(3-胆酰胺丙基)二甲基铵基]-2-羟基-1-丙烷磺酸从新生大鼠肾膜中溶解后,血管紧张素II(Ang II)AT2受体被纯化了40,000倍,达到近乎同质的状态。通过与125I标记的CGP42112(一种选择性AT2配体)的竞争曲线,获得了可溶性提取物(0.32 nM)和膜(0.31 nM)相当的IC50值。可溶性提取物中与AT2受体的结合对二硫苏糖醇不敏感。AT2受体通过凝胶过滤和CGP4211琼脂糖亲和柱进一步纯化。在4℃下用5μM CGP421将Ang II AT2受体选择性洗脱,SDS/PAGE后得到一条表观分子量为71 kDa的单带。二维电泳证实了该蛋白质的纯度,并获得了5.3 - 5.5的等电点。在高盐存在下用1μM氯沙坦处理柱子后,在室温下用5 nM 125I标记的CGP42112对AT2受体进行从亲和柱的高选择性洗脱。交联后,获得了一种具有相似分子量和等电点的主要标记蛋白质。放射性标记蛋白质的解离对氯沙坦不敏感,但被CGP42112、PD123177、Ang II和[Sar1]Ang II增强。总之,Ang II AT2受体通过CGP42112亲和色谱和选择性洗脱进行了纯化,并保留了颗粒受体的药理学特异性。