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通过跨膜电泳加速蛋白质中十二烷基硫酸钠的消耗:焦耳热的影响

Accelerated SDS depletion from proteins by transmembrane electrophoresis: Impacts of Joule heating.

作者信息

Unterlander Nicole, Doucette Alan Austin

机构信息

Department of Chemistry, Dalhousie University, Halifax, Nova Scotia, Canada.

出版信息

Electrophoresis. 2018 Jun;39(11):1349-1356. doi: 10.1002/elps.201700410. Epub 2018 Mar 1.

Abstract

SDS plays a key role in proteomics workflows, including protein extraction, solubilization and mass-based separations (e.g. SDS-PAGE, GELFrEE). However, SDS interferes with mass spectrometry and so it must be removed prior to analysis. We recently introduced an electrophoretic platform, termed transmembrane electrophoresis (TME), enabling extensive depletion of SDS from proteins in solution with exceptional protein yields. However, our prior TME runs required 1 h to complete, being limited by Joule heating which causes protein aggregation at higher operating currents. Here, we demonstrate effective strategies to maintain lower TME sample temperatures, permitting accelerated SDS depletion. Among these strategies, the use of a magnetic stir bar to continuously agitate a model protein system (BSA) allows SDS to be depleted below 100 ppm (>98% removal) within 10 min of TME operations, while maintaining exceptional protein recovery (>95%). Moreover, these modifications allow TME to operate without any user intervention, improving throughput and robustness of the approach. Through fits of our time-course SDS depletion curves to an exponential model, we calculate SDS depletion half-lives as low as 1.2 min. This promising electrophoretic platform should provide proteomics researchers with an effective purification strategy to enable MS characterization of SDS-containing proteins.

摘要

十二烷基硫酸钠(SDS)在蛋白质组学工作流程中起着关键作用,包括蛋白质提取、溶解和基于质量的分离(如SDS聚丙烯酰胺凝胶电泳、自由流动电泳)。然而,SDS会干扰质谱分析,因此在分析前必须将其去除。我们最近推出了一种电泳平台,称为跨膜电泳(TME),能够从溶液中的蛋白质中大量去除SDS,且蛋白质产率极高。然而,我们之前的TME运行需要1小时才能完成,这受到焦耳热的限制,焦耳热会在较高的工作电流下导致蛋白质聚集。在此,我们展示了保持较低TME样品温度的有效策略,从而实现加速去除SDS。在这些策略中,使用磁力搅拌棒持续搅拌模型蛋白质系统(牛血清白蛋白),可使SDS在TME操作10分钟内被消耗至100 ppm以下(去除率>98%),同时保持极高的蛋白质回收率(>95%)。此外,这些改进使TME能够在无需任何用户干预的情况下运行,提高了该方法的通量和稳健性。通过将我们的SDS消耗时间进程曲线拟合到指数模型,我们计算出SDS消耗半衰期低至1.2分钟。这个有前景的电泳平台应该为蛋白质组学研究人员提供一种有效的纯化策略,以实现对含SDS蛋白质的质谱表征。

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