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

机译:注射器 - 推动膜吸收作为临床蛋白质组学尿液制剂的简单快速方法

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Background: The analysis of urinary proteome might reveal biomarkers of clinical value. However, current methods 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. , 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. In addition, protein absorbed on nitrocellulose harvested from the SPMA procedure could be stored as a dried membrane at room temperature for at least 1-month without protein degradation or modification. Conclusions: SPMA is a simple rapid method of preparing urine for downstream proteomic analysis. Because of it is highly accessible and has long storage duration, this technique holds potential benefit for large-scale multi-center research and future development of clinical investigation based upon urinary proteomic analysis.
机译:背景:尿蛋白质组的分析可能揭示临床价值的生物标志物。然而,目前的尿液制剂用于下游蛋白质组学分析的方法是复杂的,耗时的和/或昂贵的。本研究旨在开发一种稳健,简单,廉价且易于可获得的尿液制备方法,以促进临床蛋白质组学工作流程。结果:通过5-mL医用注射器和蛋白质可吸收膜的组合成功开发了注射器 - 推膜吸收(SPMS)。比较三个膜I.,硝酸纤维素,聚偏二氟化乙烯(PVDF)和Whatman NO。 ,硝酸纤维素与SPMA(硝酸纤维素-PMMS)联合,提供了最大的蛋白质组型材的质量,如2-de所示。与三种电流尿制剂方法(即超滤,透析/冻干和沉淀)系统地进行蛋白质组型材的质量和硝化纤维素-SPMS的性能。虽然不同的尿液制剂方法提供了可相当的蛋白质组质量,但硝化纤维素-PMMS由于可接受的回收率,工作量减少,工作时间短,高可访问性和低单位成本而具有更好的工作性能。此外,在从SPMA程序收获的硝酸纤维素上吸收的蛋白质可以在室温下作为干燥的膜储存至少1个月而没有蛋白质降解或改性。结论:SPMA是一种制备下游蛋白质组学分析尿液的简单快速方法。由于它是高度访问,并且存储持续时间长,因此基于泌尿蛋白质组学分析,该技术对大规模的多中心研究和未来发展的潜在益处。

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