Kalaiselvi P, Udayapriya K L, Selvam R
Department of Medical Biochemistry, Dr ALM Post Graduate Institute of Basic Medical Sciences, University of Madras, Chennai, India.
BJU Int. 1999 Jun;83(9):919-23. doi: 10.1046/j.1464-410x.1999.00084.x.
To study the effect of urinary uric acid-binding proteins of controls and stone formers on calcium oxalate crystal nucleation and aggregation.
Urine samples were collected over 24 h from 20 stone formers and from 20 age-matched normal controls. Uric acid crystallization was induced by adding equal volumes of 2.5 mmol/L uric acid. The bound proteins were separated on a cellulose column, and by sodium dodecyl sulphate-polyacrylamide gel electrophoresis. The effect of the separated fractions on calcium oxalate crystal nucleation and aggregation was assessed.
The protein bound to unit mass of uric acid crystals was higher in hyperoxaluric urine than in control urine. On cellulose-column separation, the uric acid-crystal binding proteins produced three major protein peaks, i.e. fraction I (buffer), fraction II (0.05 mol/L sodium chloride in Tris-HCl buffer) and fraction III (0.3 mol/L sodium chloride in buffer), with a minor peak obtained on elution with increasing concentrations of sodium chloride in Tris-HCl buffer (pH 7.0). Fraction I derived from either stone formers or controls promoted calcium oxalate crystallization. Fraction II from the control samples was a strong inhibitor, whereas hyperoxaluric fraction II was less inhibitory.
Uric acid-binding proteins isolated either from the urine of stone formers or controls modulated calcium oxalate crystal growth. Proteins isolated from stone formers were less inhibitory of crystal nucleation and aggregation. These proteins may act as a bridge, leading to the epitaxial deposition of calcium oxalate over a urate core.
研究对照组和结石形成者尿液中尿酸结合蛋白对草酸钙晶体成核和聚集的影响。
从20名结石形成者和20名年龄匹配的正常对照者中收集24小时尿液样本。通过加入等体积的2.5 mmol/L尿酸诱导尿酸结晶。结合蛋白在纤维素柱上分离,并通过十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳分离。评估分离组分对草酸钙晶体成核和聚集的影响。
高草酸尿中与单位质量尿酸晶体结合的蛋白高于对照尿液。在纤维素柱分离中,尿酸晶体结合蛋白产生三个主要蛋白峰,即组分I(缓冲液)、组分II(Tris - HCl缓冲液中的0.05 mol/L氯化钠)和组分III(缓冲液中的0.3 mol/L氯化钠),在Tris - HCl缓冲液(pH 7.0)中用浓度递增的氯化钠洗脱时获得一个小峰。来自结石形成者或对照者的组分I促进草酸钙结晶。对照样本的组分II是一种强抑制剂,而高草酸尿组分II的抑制作用较小。
从结石形成者或对照者尿液中分离的尿酸结合蛋白调节草酸钙晶体生长。从结石形成者中分离的蛋白对晶体成核和聚集的抑制作用较小。这些蛋白可能充当桥梁,导致草酸钙在尿酸盐核心上的外延沉积。