Zick Y, Rees-Jones R W, Taylor S I, Gorden P, Roth J
J Biol Chem. 1984 Apr 10;259(7):4396-400.
Four polyclonal antisera directed against the insulin receptor were tested for their capability to activate the tyrosine-specific protein kinase associated with the receptor. All four antisera were shown to inhibit insulin binding to the receptor in cultured human lymphoblastoid cells and to stimulate lipogenesis in isolated rat adipocytes. Although two antisera (B-d, B-8) stimulated the activity of the tyrosine kinase of partially purified receptor preparations from rat liver, two other antisera (B-2 and B-10) failed to do so. This failure could not be explained by lack of antibody binding to receptor, by interference with the receptor as a substrate for the kinase, or by blocking of the enzyme's active site. We conclude that these two antireceptor antibodies bind to the receptor but fail to activate the kinase. The simplest interpretation of these observations is that activation of the tyrosine-specific protein kinase might not be an obligatory step in coupling insulin binding to insulin action. However, it is also possible that the mechanism by which polyclonal antireceptor antisera mimic insulin's bioactivity may differ from the mechanism of action of insulin itself.
检测了四种针对胰岛素受体的多克隆抗血清激活与该受体相关的酪氨酸特异性蛋白激酶的能力。结果显示,所有四种抗血清均能抑制胰岛素与培养的人淋巴母细胞样细胞中受体的结合,并刺激分离的大鼠脂肪细胞中的脂肪生成。尽管两种抗血清(B-d、B-8)能刺激大鼠肝脏部分纯化的受体制剂中酪氨酸激酶的活性,但另外两种抗血清(B-2和B-10)却不能。这种失败不能用抗体与受体结合不足、对作为激酶底物的受体的干扰或酶活性位点的阻断来解释。我们得出结论,这两种抗受体抗体与受体结合,但未能激活激酶。对这些观察结果最简单的解释是,酪氨酸特异性蛋白激酶的激活可能不是胰岛素结合与胰岛素作用偶联的必要步骤。然而,多克隆抗受体抗血清模拟胰岛素生物活性的机制也可能与胰岛素本身的作用机制不同。