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A Sensitive Microbead-Based Organic Media-Assisted Method for Proteomics Sample Preparation from Dilute and Denaturing Solutions

机译:一种敏感的微珠基有机介质辅助方法,用于稀释和变性溶液的蛋白质组学样品制备

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We developed a robust and sensitive sample preparation method for proteomics termed microbead-based and organic-media-assisted proteolysis strategy (BOPs). BOPs combines two advantages of current techniques, (1) unbiased binding of reversed-phase polymeric microbeads to any type of protein and (2) enhanced trypsin digestion efficiency in CH3CN aqueous solvent systems, into a single-tube workflow. Compared with conventional techniques, this method effectively"concentrates proteins and improves proteolytic digestion, and can, be used with submicromolar protein samples in dilute or denaturing solutions, such as 70% formic acid, 8 M urea, or. 7 M guanidine hydrochloride without any sample pretreatment. Proteome analysis of single Caenorhabditis elegans organisms demonstrates that BOPs has the sensitivity, reproducibility, and unbiasednesS required to characterize worm proteins at a single organism level. We also show that, by simply incorporating an acetone washing step for detergent removal; BOPs is applicable to low concentration samples contaminated with a variety of detergents, including sodium dodecyl sulfate, with negligible protein loss. Moreover, the utility of this modification has also been demonstrated through proteomic characterization of 2000 human (HEK293T) cells lysed using 1% Triton X-100. The simplicity and availability of the present BOPs make it especially attractive for next-stage proteomics of rare and sample-limited systems.
机译:我们开发了一种稳健且敏感的蛋白质组学样品制备方法,其称为微珠基和有机介质辅助蛋白水解策略(BOPS)。 BOPS结合了电流技术的两个优点,(1)将反相聚合物微珠的任何类型的蛋白质和(2)胰蛋白酶水溶液中的胰蛋白酶消化效率的无偏,进入单管工作流程中的胰蛋白酶消化效率。与常规技术相比,该方法有效地“浓缩蛋白质并改善蛋白水解消化,并且可以与稀释剂或变性溶液中的亚微粒摩尔蛋白样品一起使用,例如70%甲酸,8米尿素或。盐酸盐7m胍盐酸盐。没有任何样品预处理。单个caenorhabdis的蛋白叶杆菌生物的蛋白质组分析表明,在单一的生物体水平中表征蠕虫蛋白所需的敏感性,再现性和无偏见。我们还表明,通过简单地掺入丙酮洗涤步骤以进行洗涤剂去除; BOPS是适用于含有各种洗涤剂的低浓度样品,包括十二烷基硫酸钠,具有可忽略的蛋白质损失。此外,通过使用1%Triton X-裂解的2000人(HEK293T)细胞的蛋白质表征,还证明了这种改性的效用。 100.目前的简单性和可用性使其特别是attrac对罕见和样品限制系统的下一阶段蛋白质组学的影响。

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