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Multi-mode acquisition (MMA): An MS/MS acquisition strategy for maximizing selectivity, specificity and sensitivity of DIA product ion spectra

机译:多模式采集(MMA):一种MS / MS采集策略,用于最大化D​​IA产物离子谱的选择性,特异性和灵敏度

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摘要

In proteomics studies, it is generally accepted that depth of coverage and dynamic range is limited in data-directed acquisitions. The serial nature of the method limits both sensitivity and the number of precursor ions that can be sampled. To that end, a number of data-independent acquisition (DIA) strategies have been introduced with these methods, for the most part, immune to the sampling issue; nevertheless, some do have other limitations with respect to sensitivity. The major limitation with DIA approaches is interference, i.e., MS/MS spectra are highly chimeric and often incapable of being identified using conventional database search engines. Utilizing each available dimension of separation prior to ion detection, we present a new multi-mode acquisition (MMA) strategy multiplexing both narrowband and wideband DIA acquisitions in a single analytical workflow. The iterative nature of the MMA workflow limits the adverse effects of interference with minimal loss in sensitivity. Qualitative identification can be performed by selected ion chromatograms or conventional database search strategies.
机译:在蛋白质组学研究中,普遍接受的是,数据定向采集的覆盖深度和动态范围是有限的。该方法的串行性质限制了灵敏度和可以采样的前体离子的数量。为此,采用这些方法引入了许多数据独立获取(DIA)策略,大部分情况下不受采样问题的影响。但是,有些在灵敏度方面确实存在其他限制。 DIA方法的主要局限性是干扰,即MS / MS光谱是高度嵌合的,通常无法使用常规数据库搜索引擎进行识别。利用离子检测之前分离的每个可用维度,我们提出了一种新的多模式采集(MMA)策略,可在单个分析工作流程中对窄带和宽带DIA采集进行多路复用。 MMA工作流程的迭代性质以最小的灵敏度损失限制了干扰的不利影响。定性鉴定可以通过选择的离子色谱图或常规数据库搜索策略进行。

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