Sani B P, Singh R K, Reddy L G, Gaub M P
Kettering-Meyer Laboratories, Southern Research Institute, Birmingham, Alabama 35255.
Arch Biochem Biophys. 1990 Nov 15;283(1):107-13. doi: 10.1016/0003-9861(90)90619-a.
Nuclear receptors (RARs) for retinoic acid (RA) are considered to be the ultimate mediators of the action of RA in the control of cell differentiation and inhibition of tumorigenesis. We have isolated and partially purified and characterized RAR from a RA-responsive tissue, chick embryo skin. The purification steps included Affi-Gel blue chromatography, ultrafiltration, size exclusion chromatography, and preparative isoelectric focusing. The electrofocusing of RAR-[3H]RA complex in ampholines (pH 3-10) revealed that the receptors have an isoelectric pH of 7.5. Whereas pronase-digested the RAR-[3H]RA complex completely, DNase showed 20-35% and RNase showed negligible digestive action on the complex. The ligand binding to RAR was completely inhibited by a mercury compound. RAR-alpha- and RAR-beta-specific antibodies, on Western blot analysis, immunoreacted with a protein having a molecular weight of 50,000, presumably RAR. Binding affinity studies revealed that biologically active analogs of RA with a free COOH group (e.g., 13-cis-RA, RO-13-7410, Ch 55, and Am 80) showed, like RA, high binding affinity for RAR, whereas biologically ineffective analogs of RA (e.g., furyl and pyridyl) were poor binders. Other groups of retinoids, in which the COOH group was either lacking or blocked, did not bind to RAR whether or not they were biologically active.
维甲酸(RA)的核受体(RARs)被认为是RA在控制细胞分化和抑制肿瘤发生过程中发挥作用的最终介质。我们已经从一种对RA有反应的组织——鸡胚皮肤中分离、部分纯化并鉴定了RAR。纯化步骤包括Affi-Gel蓝琼脂糖凝胶层析、超滤、尺寸排阻层析和制备性等电聚焦。RAR-[3H]RA复合物在两性电解质(pH 3 - 10)中的电聚焦显示,这些受体的等电点pH为7.5。链霉蛋白酶能完全消化RAR-[3H]RA复合物,而脱氧核糖核酸酶对该复合物有20 - 35%的消化作用,核糖核酸酶对该复合物的消化作用可忽略不计。一种汞化合物能完全抑制配体与RAR的结合。在蛋白质免疫印迹分析中,RAR-α和RAR-β特异性抗体与一种分子量为50,000的蛋白质发生免疫反应,推测该蛋白质为RAR。结合亲和力研究表明,具有游离COOH基团的RA生物活性类似物(如13 - 顺式RA、RO - 13 - 7410、Ch 55和Am 80)与RA一样,对RAR具有高结合亲和力,而RA的生物无效类似物(如呋喃基和吡啶基)则是弱结合剂。其他类视黄醇组,无论其是否具有生物活性,只要COOH基团缺失或被阻断,就不会与RAR结合。