Engl J, Moule M, Yip C C
Banting and Best Department of Medical Research, University of Toronto, Ontario, Canada.
Biochem Biophys Res Commun. 1994 Jun 30;201(3):1439-44. doi: 10.1006/bbrc.1994.1864.
Autophosphorylation of insulin receptors from human placental membranes prepared with iodoacetamide was more than double that of control receptors prepared without iodoacetamide. Dithiothreitol (DTT) treatment of control receptors prepared without iodoacetamide resulted in increased autophosphorylation. However, DTT was without effect on insulin receptors prepared with iodoacetamide. Phosphopeptide analysis showed that while 32P-labeling of all of the phosphopeptides was increased in insulin receptors from membranes prepared with iodoacetamide, two additional phosphopeptides were detected and identified as deriving from the juxtamembrane domain, containing tyrosine residue 960. Similar results were produced by DTT treatment of control insulin receptors. These observations suggest that a thiol(s) may be involved in insulin receptor autophosphorylation in the juxtamembrane domain.
用碘乙酰胺制备的人胎盘膜胰岛素受体的自磷酸化程度是未用碘乙酰胺制备的对照受体的两倍多。用二硫苏糖醇(DTT)处理未用碘乙酰胺制备的对照受体,会导致自磷酸化增加。然而,DTT对用碘乙酰胺制备的胰岛素受体没有影响。磷酸肽分析表明,在用碘乙酰胺制备的膜的胰岛素受体中,所有磷酸肽的32P标记都增加了,同时还检测到另外两个磷酸肽,并确定它们来自含有酪氨酸残基960的近膜结构域。对对照胰岛素受体进行DTT处理也产生了类似的结果。这些观察结果表明,一个或多个巯基可能参与胰岛素受体近膜结构域的自磷酸化。