磷酸蛋白质组学
再现性
工作流程
串联质谱法
软件
数据挖掘
计算机科学
磷酸化
质谱法
磷酸肽
色谱法
化学
数据库
蛋白质磷酸化
操作系统
蛋白激酶A
生物化学
作者
Ana Martínez-Val,Dorte B. Bekker-Jensen,Alexander Hogrebe,Jesper V. Olsen
出处
期刊:Methods in molecular biology
日期:2021-01-01
卷期号:: 95-107
被引量:35
标识
DOI:10.1007/978-1-0716-1641-3_6
摘要
Data-independent acquisition (DIA) for liquid chromatography tandem mass spectrometry (LC-MS/MS) can improve the depth and reproducibility of the acquired proteomics datasets. DIA solves some limitations of the conventional data-dependent acquisition (DDA) strategy, for example, bias in intensity-dependent precursor selection and limited dynamic range. These advantages, together with the recent developments in speed, sensitivity, and resolution in MS technology, position DIA as a great alternative to DDA. Recently, we demonstrated that the benefits of DIA are extendable to phosphoproteomics workflows, enabling increased depth, sensitivity, and reproducibility of our analysis of phosphopeptide-enriched samples. However, computational data analysis of phospho-DIA samples have some specific challenges and requirements to the software and downstream processing workflows. A step-by-step guide to analyze phospho-DIA raw data using either spectral libraries or directDIA in Spectronaut is presented here. Furthermore, a straightforward protocol to perform differential phosphorylation site analysis using the output results from Spectronaut is described.
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