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使用自动工作站进行质谱分析的血浆样品制备

A Plasma Sample Preparation for Mass Spectrometry using an Automated Workstation.

作者信息

Fu Qin, Johnson Casey W, Wijayawardena Bhagya K, Kowalski Michael P, Kheradmand Miranda, Van Eyk Jennifer E

机构信息

Advanced Clinical Biosystems Institute, Smidt Heart institute, Cedars Sinai Medical Center.

Beckman Coulter Life Sciences.

出版信息

J Vis Exp. 2020 Apr 24(158). doi: 10.3791/59842.

DOI:10.3791/59842
PMID:32391810
Abstract

Sample preparation for mass spectrometry analysis in proteomics requires enzymatic cleavage of proteins into a peptide mixture. This process involves numerous incubation and liquid transfer steps in order to achieve denaturation, reduction, alkylation, and cleavage. Adapting this workflow onto an automated workstation can increase efficiency and reduce coefficients of variance, thereby providing more reliable data for statistical comparisons between sample types. We previously described an automated proteomic sample preparation workflow. Here, we report the development of a more efficient and better controlled workflow with the following advantages: 1) The number of liquid transfer steps is reduced from nine to six by combining reagents; 2) Pipetting time is reduced by selective tip pipetting using a 96-position pipetting head with multiple channels; 3) Potential throughput is increased by the availability of up to 45 deck positions; 4) Complete enclosure of the system provides improved temperature and environmental control and reduces the potential for contamination of samples or reagents; and 5) The addition of stable isotope labeled peptides, as well as β-galactosidase protein, to each sample makes monitoring and quality control possible throughout the entire process. These hardware and process improvements provide good reproducibility and improve intra-assay and inter-assay precision (CV of less than 20%) for LC-MS based protein and peptide quantification. The entire workflow for digesting 96 samples in a 96-well plate can be completed in approximately 5 hours.

摘要

蛋白质组学中用于质谱分析的样品制备需要将蛋白质酶解为肽混合物。这个过程涉及许多孵育和液体转移步骤,以实现变性、还原、烷基化和酶解。将此工作流程应用于自动化工作站可以提高效率并降低变异系数,从而为不同样品类型之间的统计比较提供更可靠的数据。我们之前描述了一种自动化蛋白质组学样品制备工作流程。在此,我们报告一种更高效且控制更好的工作流程的开发,其具有以下优点:1)通过合并试剂,液体转移步骤从九个减少到六个;2)使用具有多个通道的96孔移液器头进行选择性吸头移液器操作,减少了移液时间;3)多达45个台面位置的可用性提高了潜在通量;4)系统的完全封闭提供了更好的温度和环境控制,并降低了样品或试剂被污染的可能性;5)向每个样品中添加稳定同位素标记的肽以及β-半乳糖苷酶蛋白,使得在整个过程中进行监测和质量控制成为可能。这些硬件和流程改进提供了良好的重现性,并提高了基于液相色谱-质谱的蛋白质和肽定量分析的批内和批间精密度(变异系数小于20%)。在96孔板中消化96个样品的整个工作流程大约可在5小时内完成。

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