Mazur Paulina, Dumnicka Paulina, Tisończyk Joanna, Ząbek-Adamska Anna, Drożdż Ryszard
Department of Medical Diagnostics, Faculty of Pharmacy, Jagiellonian University Medical College, 30-688 Kraków, Poland.
Department of Diagnostics, University Hospital in Kraków, 30-688 Kraków, Poland.
Diagnostics (Basel). 2023 Apr 23;13(9):1513. doi: 10.3390/diagnostics13091513.
Proteinuria is an important sign of kidney diseases. Different protein patterns in urine associated with glomerular, tubular and overload proteinuria may be differentiated using the immunochemical detection of indicator proteins or via urinary proteins electrophoresis. Our aim was to characterize sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) using commercially available 4-20% gradient gels as a method to detect and differentiate proteinuria. Our laboratory-based study used excess urine samples collected for routine diagnostic purposes from adult patients of a tertiary-care hospital, including patients with albumin/creatinine < 30 mg/g and patients with dipstick proteinuria. The limit of albumin detection was estimated to be 3 mg/L. In 93 samples with albumin/creatinine < 30 mg/g, an albumin fraction was detected in 87% of samples with a minimum albumin concentration of 2.11 mg/L. The separation of 300 urine samples of patients with proteinuria revealed distinct protein patterns differentiated using the molecular weights of the detected proteins: glomerular (albumin and higher molecular weights) and two types of tubular proteinuria ("upper" ≥20 kDa and "lower" with lower molecular weights). These patterns were associated with different values of the glomerular filtration rate (median 66, 71 and 31 mL/min/1.72 m, respectively, = 0.004) and different proportions of multiple myeloma and nephrological diagnoses. As confirmed using tandem mass spectrometry and western blot, the SDS-PAGE protein fractions contained indicator proteins including immunoglobulin G, transferrin (glomerular proteinuria), α1-microglobulin, retinol-binding protein, neutrophil gelatinase-associated lipocalin, cystatin C, and β2-microglobulin (tubular), immunoglobulin light chain, myoglobin, and lysozyme (overflow). SDS-PAGE separation of urine proteins on commercially available 4-20% gradient gels is a reliable technique to diagnose proteinuria and differentiate between its main clinically relevant types.
蛋白尿是肾脏疾病的重要标志。利用指示蛋白的免疫化学检测或通过尿蛋白电泳,可以区分与肾小球性、肾小管性和溢出性蛋白尿相关的不同尿蛋白模式。我们的目的是使用市售的4-20%梯度凝胶表征十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE),作为一种检测和区分蛋白尿的方法。我们基于实验室的研究使用了从一家三级护理医院的成年患者收集的多余尿液样本用于常规诊断目的,包括白蛋白/肌酐<30 mg/g的患者和试纸法蛋白尿患者。白蛋白检测限估计为3 mg/L。在93份白蛋白/肌酐<30 mg/g的样本中,87%的样本检测到白蛋白组分,最低白蛋白浓度为2.11 mg/L。对300份蛋白尿患者的尿液样本进行分离,根据检测到的蛋白质分子量揭示了不同的蛋白模式:肾小球性(白蛋白和更高分子量)和两种类型的肾小管性蛋白尿(“上”≥20 kDa和分子量较低的“下”型)。这些模式与不同的肾小球滤过率值(中位数分别为66、71和31 mL/min/1.72 m²,P = 0.004)以及多发性骨髓瘤和肾脏病诊断的不同比例相关。正如串联质谱和western blot所证实的,SDS-PAGE蛋白组分包含指示蛋白,包括免疫球蛋白G、转铁蛋白(肾小球性蛋白尿)、α1-微球蛋白、视黄醇结合蛋白、中性粒细胞明胶酶相关脂质运载蛋白、胱抑素C和β2-微球蛋白(肾小管性)、免疫球蛋白轻链、肌红蛋白和溶菌酶(溢出性)。在市售的4-20%梯度凝胶上对尿蛋白进行SDS-PAGE分离是一种可靠的技术,可用于诊断蛋白尿并区分其主要临床相关类型。