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Cost-effective generation of precise label-free quantitative proteomes in high-throughput by microLC and data-independent acquisition

机译:通过Microolc和Data-Insworation的高吞吐量在高吞吐量中经济高效地产生精确的无标签定量蛋白质

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Quantitative proteomics is key for basic research, but needs improvements to satisfy an increasing demand for large sample series in diagnostics, academia and industry. A switch from nanoflowrate to microflowrate chromatography can improve throughput and reduce costs. However, concerns about undersampling and coverage have so far hampered its broad application. We used a QTOF mass spectrometer of the penultimate generation (TripleTOF5600), converted a nanoLC system into a microflow platform, and adapted a SWATH regime for large sample series by implementing retention time- and batch correction strategies. From 3?μg to 5?μg of unfractionated tryptic digests that are obtained from proteomics-typical amounts of starting material, microLC-SWATH-MS quantifies up to 4000 human or 1750 yeast proteins in an hour or less. In the acquisition of 750 yeast proteomes, retention times varied between 2% and 5%, and quantified the typical peptide with 5–8% signal variation in replicates, and below 20% in samples acquired over a five-months period. Providing precise quantities without being dependent on the latest hardware, our study demonstrates that the combination of microflow chromatography and data-independent acquisition strategies has the potential to overcome current bottlenecks in academia and industry, enabling the cost-effective generation of precise quantitative proteomes in large scale.
机译:定量蛋白质组学是基础研究的关键,但需要改进,以满足对诊断,学术界和工业的大型样品系列的日益增长的需求。从纳米酚转换为微氟化色谱的切换可以提高产量并降低成本。然而,对欠采样和覆盖范围的担忧迄今为止阻碍了其广泛的应用。我们使用倒数第二发电(Tripletof5600)的QTOF质谱仪,将NANOLC系统转换为微射线平台,并通过实现保留时间和批量校正策略来调整大型样品系列的SWATH制度。从3?μg到5?μg从蛋白质组学的起始材料中获得的未分压胰蛋白酶消化,Microolc-swath-ms在一小时或更短的时间内量化高达4000名人或1750酵母蛋白。在750酵母蛋白质组的采集中,保留次数在2%和5%之间变化,并且量化了典型的肽,在五个月内获得的样品中的5-8%的信号变异,低于20%。我们的研究提供了精确的数量而不依赖于最新的硬件,我们的研究表明,微射线色谱和数据无关的采集策略的组合有可能克服学术界和工业中的当前瓶颈,使大量的精确定量蛋白质产生的经济有效地产生规模。

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