Kato M, Nakayama H, Makita Z, Aoki S, Kuroda Y, Misawa K, Yoshida H, Yanagisawa K, Nakagawa S
2nd Department of Internal Medicine, Hokkaido University School of Medicine, Sapporo, Japan.
Horm Metab Res. 1989 May;21(5):245-8. doi: 10.1055/s-2007-1009204.
We have developed a radioimmunoassay (RIA) for nonenzymatically glycated serum proteins. The polyclonal antibodies prepared against reduced glycated human albumin were specific for the glucitollysine residues of serum proteins. Serum proteins from diabetic patients (n = 25) contained 5.3 +/- 2.8 nmoles of glucitollysine/mg protein, compared to 2.0 +/- 0.2 in controls (n = 20). The intra- and inter-assay variables were 3.2-6.2% and 4.4-8.6%, respectively. Results from this assay procedure correlated well with those from the boronate affinity chromatography procedure (r = 0.94; P less than 0.001). The data suggested that diabetic serum proteins contained at least 2.5 times as much immunochemically detectable glucitollysine residures as normal serum proteins after reduction of the proteins with sodium borohydride.
我们已经开发出一种用于非酶糖基化血清蛋白的放射免疫测定法(RIA)。针对还原型糖基化人白蛋白制备的多克隆抗体对血清蛋白的葡糖胺赖氨酸残基具有特异性。糖尿病患者(n = 25)的血清蛋白含有5.3±2.8纳摩尔葡糖胺赖氨酸/毫克蛋白,而对照组(n = 20)为2.0±0.2。测定内和测定间的变量分别为3.2 - 6.2%和4.4 - 8.6%。该测定程序的结果与硼酸酯亲和色谱法的结果相关性良好(r = 0.94;P < 0.001)。数据表明,在用硼氢化钠还原蛋白质后,糖尿病血清蛋白中免疫化学可检测到的葡糖胺赖氨酸残基含量至少是正常血清蛋白的2.5倍。