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Autopilot: An Online Data Acquisition Control System for the Enhanced High-Throughput Characterization of Intact Proteins

机译:自动驾驶仪:在线数据采集控制系统,用于增强完整蛋白的高通量表征

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The ability to study organisms by direct analysis of their proteomes without digestion via mass spectrometry has benefited greatly from recent advances in separation techniques, instrumentation, and bioinformatics. However, improvements to data acquisition logic have lagged in comparison. Past workflows for Top Down Proteomics (TDPs) have focused on high throughput at the expense of maximal protein coverage and characterization. This mode of data acquisition has led to enormous overlap in the identification of highly abundant proteins in subsequent LC-MS injections. Furthermore, a wealth of data is left underutilized by analyzing each newly targeted species as unique, rather than as part of a collection of fragmentation events on a distinct proteoform. Here, we present a major advance in software for acquisition of TDP data that incorporates a fully automated workflow able to detect intact masses, guide fragmentation to achieve maximal identification and characterization of intact protein species, and perform database search online to yield real-time protein identifications. On Pseudomonas aeruginosa, the software combines fragmentation events of the same precursor with previously obtained fragments to achieve improved characterization of the target form by an average of 42 orders of magnitude in confidence. When HCD fragmentation optimization was applied to intact proteins ions, there was an 18.5 order of magnitude gain in confidence. These improved metrics set the stage for increased proteome coverage and characterization of higher order organisms in the future for sharply improved control over MS instruments in a project- and lab-wide context.
机译:通过分离技术,仪器仪表和生物信息学的最新进展,极大地受益于通过直接分析其蛋白质组而无需通过质谱进行消化来研究生物的能力。但是,相比之下,数据采集逻辑的改进滞后了。过去的自上而下蛋白质组学(TDP)的工作流程专注于高通量,但以最大程度的蛋白质覆盖和表征为代价。这种数据采集模式已导致在随后的LC-MS进样中鉴定高度丰富的蛋白质时出现了巨大的重叠。此外,通过将每个新靶向物种分析为独特的,而不是将其作为独特蛋白形式的片段化事件集合的一部分来分析,从而使大量数据未被充分利用。在这里,我们介绍了用于采集TDP数据的软件方面的重大进展,该软件结合了能够检测完整质量,指导片段化以最大程度鉴定和鉴定完整蛋白种类并在线进行数据库搜索以产生实时蛋白的全自动工作流程标识。在铜绿假单胞菌上,该软件将同一前体的碎片事件与先前获得的碎片结合在一起,从而以平均42个数量级的置信度实现了目标形式的改进表征。当HCD碎片优化应用于完整的蛋白质离子时,置信度提高了18.5个数量级。这些改进的指标为将来增加蛋白质组覆盖率和表征高阶生物奠定了基础,以便在项目和实验室范围内显着改善对MS仪器的控制。

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