Thongboonkerd Visith, Mungdee Siriwan, Chiangjong Wararat
Medical Proteomics Unit, Office for Research and Development, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
J Proteome Res. 2009 Jun;8(6):3206-11. doi: 10.1021/pr900127x.
The urine has become one of the most widely used clinical samples for biomarker discovery. The pH of human urine may vary largely from 4.5 to 8.0. Previously, it was questionable whether the urine pH would affect proteome analysis and whether the urine pH needed to be adjusted prior to proteome analysis remained unclear. We therefore performed a systematic analysis of the effect of urine pH on proteome profile. Midstream second morning and random afternoon urine samples were collected from 5 males and 5 females who were healthy and had no recent medication. After removal of cells and debris by low-speed centrifugation, pH levels of individual samples were measured and urinary proteins were isolated by 75% ethanol precipitation. Equally loaded 100 microg of proteins from individual samples were resolved in 2-DE (linear pH 3-10) and visualized with SYPRO Ruby fluorescence stain. There was no significant correlation between difference in the morning versus afternoon urine pH (DeltapH) and %match of protein spots derived from morning versus afternoon urine samples in individual samples (Pearson's r = 0.074; p = 0.839). In parallel, all individual samples with equal volume were pooled. The pH of the pooled urine was adjusted to 4-10 and urinary proteome profiles were analyzed as for individual samples. ANOVA with Tukey's posthoc multiple comparisons showed no significant differences in total number of detected spots and %match among various pH levels. Our data suggest that the urine pH has no significant effects on urinary proteome profile and thus needs no adjustment prior to gel-based proteome analysis.
尿液已成为生物标志物发现中使用最广泛的临床样本之一。人体尿液的pH值在4.5至8.0之间变化很大。以前,尿液pH值是否会影响蛋白质组分析以及在蛋白质组分析之前是否需要调整尿液pH值尚不清楚。因此,我们对尿液pH值对蛋白质组图谱的影响进行了系统分析。从5名健康且近期未用药的男性和5名女性中收集晨尿中段和随机下午尿液样本。通过低速离心去除细胞和碎片后,测量各个样本的pH值,并通过75%乙醇沉淀分离尿液蛋白质。将来自各个样本的等量100微克蛋白质在2-DE(线性pH 3-10)中进行分离,并用SYPRO Ruby荧光染色进行可视化。在各个样本中,晨尿与下午尿pH值的差异(ΔpH)与晨尿和下午尿样本中蛋白质斑点的匹配百分比之间没有显著相关性(Pearson相关系数r = 0.074;p = 0.839)。同时,将所有等体积的个体样本合并。将合并尿液的pH值调整至4-10,并像分析个体样本一样分析尿液蛋白质组图谱。采用Tukey事后多重比较的方差分析显示,在不同pH水平下,检测到的斑点总数和匹配百分比没有显著差异。我们的数据表明,尿液pH值对尿液蛋白质组图谱没有显著影响,因此在基于凝胶的蛋白质组分析之前无需调整。