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Syringe-push membrane absorption as a simple rapid method of urine preparation for clinical proteomics

机译:注射器推入式膜吸收作为临床蛋白质组学尿液制备的简单快速方法

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Background: The analysis of urinary proteome might reveal biomarkers of clinical value. However, current method of urine preparation for down-stream proteomic analysis are complicated, time-consuming, and/or expensive. This study aims to develop a robust, simple, inexpensive and readily accessible urine preparation method to facilitate clinical proteomic workflow.Result: Syringe-push membrane absorption (SPMA) was successfully developed by a combination of 5-ml medical syringe and protein-absorbable membrane. Comparing three membranes i.e., nitrocellulose, polyvinylidene difluoride (PVDF) and Whatman no.1, nitrocellulose combined with SPMA (nitrocellulose-SPMA) provided the greatest quality of proteome profile as demonstrated by 2-DE. The quality of the proteome profile and the performance of nitrocellulose-SPMA were systematically compared with three current methods of urine preparation (i.e., ultrafiltration, dialysis/ lyophilization and precipitation). While different methods of urine preparation provided comparable proteome quality, nitrocellulose-SPMA had better working performance due to acceptable recovery yield, less workload, short working time, high accessibility and low unit cost.
机译:背景:尿蛋白的分析可能揭示具有临床价值的生物标志物。然而,用于下游蛋白质组学分析的当前尿液制备方法复杂,费时和/或昂贵。这项研究旨在开发一种鲁棒,简单,廉价且易于使用的尿液制备方法,以促进临床蛋白质组学工作流程。结果:结合5 ml医用注射器和蛋白质可吸收膜成功开发了注射器推膜吸收(SPMA) 。比较三层膜,即硝酸纤维素膜,聚偏二氟乙烯(PVDF)和Whatman No.1,硝酸纤维素膜与SPMA(硝酸纤维素膜-SPMA)的结合提供了最优质的蛋白质组图谱,如2-DE所示。系统地将蛋白质组图谱的质量和硝酸纤维素SPMA的性能与三种当前的尿液制备方法(即超滤,透析/冻干和沉淀)进行了比较。尽管不同的尿液制备方法可提供可比的蛋白质组质量,但硝酸纤维素SPMA的回收率高,工作量少,工作时间短,可及性高且单位成本低,因此具有更好的工作性能。

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