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The Optimized Workflow for Sample Preparation in LC-MS/MS-Based Urine Proteomics

机译:基于LC-MS / MS的尿液蛋白质组学中样品制备的优化工作流程

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摘要

The sample condition is an important factor in urine proteomics with stability and accuracy. However, a general protocol of urine protein preparation in mass spectrometry analysis has not yet been established. Here, we proposed a workflow for optimized sample preparation based on methanol/chloroform (M/C) precipitation and in-solution trypsin digestion in LC-MS/MS-based urine proteomics. The urine proteins prepared by M/C precipitation showed around 80% of the protein recovery rate. The samples showed the largest number of identified proteins, which were over 1000 on average compared with other precipitation methods in LC-MS/MS-based urine proteomics. For further improvement of the workflow, the essences were arranged in protein dissolving and trypsin digestion step for the extraction of urine proteins. Addition of Ethylene diamine tetraacetic acid (EDTA) dramatically enhanced the dissolution of protein and promoted the trypsin activity in the digestion step because the treatment increased the number of identified proteins with less missed cleavage sites. Eventually, an optimized workflow was established by a well-organized strategy for daily use in the LC-MS/MS-based urine proteomics. The workflow will be of great help for several aims based on urine proteomics approaches, such as diagnosis and biomarker discovery.
机译:样品状况是尿液蛋白质组学稳定且准确的重要因素。但是,尚未建立质谱分析中尿蛋白制备的一般方案。在这里,我们提出了一种基于LC / MS / MS的尿蛋白质组学中基于甲醇/氯仿(M / C)沉淀和溶液中胰蛋白酶消化的优化样品制备的工作流程。通过M / C沉淀制备的尿蛋白显示出约80%的蛋白回收率。样品显示出鉴定出的最大数量的蛋白质,与基于LC-MS / MS的尿液蛋白质组学中的其他沉淀方法相比,平均超过1000种。为了进一步改善工作流程,将精华液安排在蛋白质溶解和胰蛋白酶消化步骤中以提取尿液蛋白质。乙二胺四乙酸(EDTA)的添加显着增强了蛋白质在消化步骤中的溶解并提高了胰蛋白酶的活性,因为这种处理增加了鉴定出的蛋白质的数量,减少了错位。最终,通过一种组织良好的策略为基于LC-MS / MS的尿液蛋白质组学的日常使用建立了优化的工作流程。该工作流程对于基于尿液蛋白质组学方法的多个目标(例如诊断和生物标志物发现)将有很大帮助。

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