Tseng L Y, Schwartz G P, Sheikh M, Chen Z Z, Joshi S, Wang J F, Nissley S P, Burke G T, Katsoyannis P G, Rechler M M
National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892.
Biochem Biophys Res Commun. 1987 Dec 16;149(2):672-9. doi: 10.1016/0006-291x(87)90420-7.
Two synthetic insulin-like compounds consisting of the B-chain of insulin linked via disulfide bonds to A chains corresponding to the A-domain or the A- and D-domains of insulin-like growth factor I (IGF-I) have been evaluated for mitogenic activity and for binding to IGF receptors and IGF carrier proteins. Both compounds are 3- to 5-fold more potent mitogens than insulin, and have a comparably increased affinity for the type I IGF receptor that mediates these mitogenic effects in chick embryo fibroblasts. Neither compound interacts with IGF carrier proteins. These results indicate that the A-domain of IGF-I is importantly involved in its growth-promoting properties.
两种合成的胰岛素样化合物已被评估其促有丝分裂活性以及与胰岛素样生长因子I(IGF-I)的IGF受体和IGF载体蛋白的结合能力。这两种化合物由胰岛素的B链通过二硫键与对应于IGF-I的A结构域或A和D结构域的A链相连。两种化合物作为促有丝分裂原的效力均比胰岛素强3至5倍,并且对I型IGF受体的亲和力也相应增加,该受体在鸡胚成纤维细胞中介导这些促有丝分裂作用。两种化合物均不与IGF载体蛋白相互作用。这些结果表明,IGF-I的A结构域对其生长促进特性具有重要作用。