G Gaslini Children Hospital, Laboratory of Pathophysiology of Uremia, Genoa, Italy.
Proteomics. 2012 Feb;12(4-5):509-15. doi: 10.1002/pmic.201100404. Epub 2012 Jan 19.
In this review, we report the evolution on experimental conditions for the analysis of normal urine based on combinatorial peptide ligand library (CPLL) treatment and successive 2-DE and 2-DE/MS analysis. The main topics are (i) definition of the urine sample requirements, (ii) optimization of the urine/ligand ratio, (iii) essay conditions, (iv) en bloc elution. Overall, normal urine protein composition as studied by 2-DE includes over 2600 spots. Relevant data on inter and intraessay reproducibility obtained by the analysis of different normal urines repeated several times are also here presented. We found a 73% reproducibility upon analysis of the same sample and 68% correspondence of protein composition among different normal urine samples. Based on the above results, we are completing the characterization with LC-MS of 249 spots. The composition of normal urine proteins after CPLLs is finally shown with the indication of those spots which are currently under identification. This map will be completed in a near future; in the meantime this would represent the basic reference sample for newly developed studies on human diseases.
在这篇综述中,我们报告了基于组合肽配体文库 (CPLL) 处理和连续 2-DE 和 2-DE/MS 分析的正常尿液分析实验条件的演变。主要主题包括:(i) 尿液样本要求的定义,(ii) 尿液/配体比例的优化,(iii) 实验条件,(iv) 整块洗脱。总的来说,通过 2-DE 研究的正常尿液蛋白质组成包括超过 2600 个斑点。通过对多次重复的不同正常尿液的分析获得的关于内和内实验可重复性的相关数据也在此呈现。我们发现对同一样本进行分析时的可重复性为 73%,而不同正常尿液样本之间蛋白质组成的对应性为 68%。基于上述结果,我们正在用 LC-MS 对 249 个斑点进行特征描述。CPLLs 处理后的正常尿液蛋白质组成最终通过指示当前正在鉴定的那些斑点来表示。该图谱将在不久的将来完成;在此期间,这将成为新的人类疾病研究的基本参考样本。