Department of Molecular Systems Biology, University of Vienna, Vienna, Austria.
Nat Protoc. 2013 Mar;8(3):595-601. doi: 10.1038/nprot.2013.013. Epub 2013 Feb 28.
Recently, new software tools have been developed for improved protein quantification using mass spectrometry (MS) data. However, there are still limitations especially in high-sample-throughput quantification methods, and most of these relate to extensive computational calculations. The mass accuracy precursor alignment (MAPA) strategy has been shown to be a robust method for relative protein quantification. Its major advantages are high resolution, sensitivity and sample throughput. Its accuracy is data dependent and thus best suited for precursor mass-to-charge precision of ∼1 p.p.m. This protocol describes how to use a software tool (ProtMAX) that allows for the automated alignment of precursors from up to several hundred MS runs within minutes without computational restrictions. It comprises features for 'ion intensity count' and 'target search' of a distinct set of peptides. This procedure also includes the recommended MS settings for complex quantitative MAPA analysis using ProtMAX (http://www.univie.ac.at/mosys/software.html).
最近,已经开发出了新的软件工具,用于使用质谱 (MS) 数据进行改进的蛋白质定量。然而,特别是在高通量定量方法中,仍然存在局限性,而且大多数与广泛的计算计算有关。质量精度前体对齐 (MAPA) 策略已被证明是一种用于相对蛋白质定量的稳健方法。其主要优点是高分辨率、灵敏度和样品通量。其准确性是数据依赖性的,因此最适合于前体质荷比精度约为 1 p.p.m。本协议描述了如何使用软件工具 (ProtMAX),该工具允许在几分钟内自动对齐多达数百个 MS 运行的前体,而不受计算限制。它包含用于“离子强度计数”和“目标搜索”一组独特肽的功能。此过程还包括使用 ProtMAX 进行复杂定量 MAPA 分析的推荐 MS 设置 (http://www.univie.ac.at/mosys/software.html)。