Lubec G, Pollak A
Ren Physiol. 1980;3(1-6):4-8. doi: 10.1159/000172733.
Glomerular basement membrane (GBM) preparations were enzymatically glucosylated and applied to proteolytic degradation by several enzymes. The split products were then characterized and quantitatively estimated by high pressure liquid chromatography. For this purpose, GBMs were isolated by a sieving and sonication method, incubated with glucose and digested with the proteases trypsin, chymotrypsin, papain, pepsin and a lysosomal preparation. Comparison of the concentrations of split products obtained by proteolytic degradation of normal and nonenzymatically glucosylated membranes showed a remarkable reduced susceptibility of the nonenzymatically glucosylated membranes, possibly due to steric hindrance or altered electrical charge of the glucosylated membrane proteins. This could be interpreted as an additional factor for accumulation of basement membrane material in the diabetic state, that not only increased basement membrane synthesis may occur but also reduced catabolism could possibly contribute to the diabetic changes.
肾小球基底膜(GBM)制剂经酶促糖基化处理后,再用几种酶进行蛋白水解降解。然后通过高压液相色谱对裂解产物进行表征和定量评估。为此,采用筛分和超声处理方法分离GBM,将其与葡萄糖一起孵育,并用蛋白酶胰蛋白酶、糜蛋白酶、木瓜蛋白酶、胃蛋白酶和溶酶体制剂进行消化。对正常膜和非酶促糖基化膜经蛋白水解降解后获得的裂解产物浓度进行比较,结果显示非酶促糖基化膜的敏感性显著降低,这可能是由于糖基化膜蛋白的空间位阻或电荷改变所致。这可以解释为糖尿病状态下基底膜物质积累的一个额外因素,即不仅可能发生基底膜合成增加,而且分解代谢减少也可能导致糖尿病性改变。