首页> 外文期刊>Clinical proteomics. >Syringe-push membrane absorption as a simple rapid method of urine preparation for clinical proteomics
【24h】

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

获取原文
获取原文并翻译 | 示例
           

摘要

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.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. 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健壮,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: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(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。另外,从SPMA程序收获的硝化纤维素上吸收的蛋白质可以在室温下作为干燥膜保存至少1个月,而不会发生蛋白质降解或修饰。结论:SPMA是制备尿液用于下游蛋白质组学分析的简单快速方法。由于它易于访问且存储时间长,因此该技术对于大规模多中心研究以及基于尿蛋白质组学分析的临床研究的未来发展具有潜在的好处。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号