Bauer H, Nagel J, Wierer D, Brunner H, Franz H E
Uremia Invest. 1985;9(2):269-75. doi: 10.3109/08860228509088219.
Urinary proteins were studied in patients after kidney transplantation during various functional states (normal function, acute rejection, chronic rejection) by two-dimensional polyacrylamide gel electrophoresis. In the first dimension, the proteins were separated according to their electric charge by isoelectric focusing, and in the second dimension according to their molecular weight by sodium dodecyl sulfate polyacrylamide gel electrophoresis. After electrophoresis the proteins were visualized using a highly sensitive silver stain technique. The combination of these methods allowed the discrimination of up to 250 protein spots in human urine, most of them unidentified up to now. Functional changes of the kidney transplants were accompanied by complex changes of the protein pattern in urine. These changes cannot be simply compared to the tubular and glomerular pattern of proteinuria which can be identified by one-dimensional sodium dodecyl sulfate electrophoresis. The 2D electrophoresis of urinary proteins may develop into a useful tool in localizing of kidney damage and in the evaluation of renal disease.
通过二维聚丙烯酰胺凝胶电泳对肾移植术后处于不同功能状态(正常功能、急性排斥反应、慢性排斥反应)的患者尿液蛋白质进行了研究。在第一维中,蛋白质通过等电聚焦根据其电荷进行分离,在第二维中通过十二烷基硫酸钠聚丙烯酰胺凝胶电泳根据其分子量进行分离。电泳后,使用高灵敏度银染技术使蛋白质可视化。这些方法的结合能够区分出人类尿液中多达250个蛋白质斑点,其中大多数至今尚未鉴定。肾移植的功能变化伴随着尿液中蛋白质图谱的复杂变化。这些变化不能简单地与通过一维十二烷基硫酸钠电泳鉴定的蛋白尿的肾小管和肾小球模式相比较。尿液蛋白质的二维电泳可能会发展成为一种用于定位肾损伤和评估肾脏疾病的有用工具。