Yates John R, Ruse Cristian I, Nakorchevsky Aleksey
Department of Chemical Physiology and Cell Biology, The Scripps Research Institute, La Jolla, California 92037, USA.
Annu Rev Biomed Eng. 2009;11:49-79. doi: 10.1146/annurev-bioeng-061008-124934.
Mass spectrometry (MS) is the most comprehensive and versatile tool in large-scale proteomics. In this review, we dissect the overall framework of the MS experiment into its key components. We discuss the fundamentals of proteomic analyses as well as recent developments in the areas of separation methods, instrumentation, and overall experimental design. We highlight both the inherent strengths and limitations of protein MS and offer a rough guide for selecting an experimental design based on the goals of the analysis. We emphasize the versatility of the Orbitrap, a novel mass analyzer that features high resolution (up to 150,000), high mass accuracy (2-5 ppm), a mass-to-charge range of 6000, and a dynamic range greater than 10(3). High mass accuracy of the Orbitrap expands the arsenal of the data acquisition and analysis approaches compared with a low-resolution instrument. We discuss various chromatographic techniques, including multidimensional separation and ultra-performance liquid chromatography. Multidimensional protein identification technology (MudPIT) involves a continuum sample preparation, orthogonal separations, and MS and software solutions. We discuss several aspects of MudPIT applications to quantitative phosphoproteomics. MudPIT application to large-scale analysis of phosphoproteins includes (a) a fractionation procedure for motif-specific enrichment of phosphopeptides, (b) development of informatics tools for interrogation and validation of shotgun phosphopeptide data, and (c) in-depth data analysis for simultaneous determination of protein expression and phosphorylation levels, analog to western blot measurements. We illustrate MudPIT application to quantitative phosphoproteomics of the beta adrenergic pathway. We discuss several biological discoveries made via mass spectrometry pipelines with a focus on cell signaling proteomics.
质谱(MS)是大规模蛋白质组学中最全面、用途最广泛的工具。在本综述中,我们将MS实验的整体框架剖析为其关键组成部分。我们讨论蛋白质组学分析的基本原理以及分离方法、仪器设备和整体实验设计等领域的最新进展。我们强调了蛋白质MS的内在优势和局限性,并根据分析目标提供了选择实验设计的大致指南。我们着重介绍了Orbitrap的多功能性,它是一种新型质量分析器,具有高分辨率(高达150,000)、高质量准确度(2 - 5 ppm)、质荷比范围达6000以及大于10³的动态范围。与低分辨率仪器相比,Orbitrap的高质量准确度扩展了数据采集和分析方法的范围。我们讨论了各种色谱技术,包括多维分离和超高效液相色谱。多维蛋白质鉴定技术(MudPIT)涉及连续的样品制备、正交分离以及MS和软件解决方案。我们讨论了MudPIT在定量磷酸蛋白质组学中的几个应用方面。MudPIT在大规模磷酸化蛋白质分析中的应用包括:(a)用于磷酸肽基序特异性富集的分级分离程序;(b)用于鸟枪法磷酸肽数据查询和验证的信息学工具开发;(c)类似于蛋白质印迹测量的用于同时测定蛋白质表达和磷酸化水平的深入数据分析。我们举例说明了MudPIT在β肾上腺素能途径定量磷酸蛋白质组学中的应用。我们讨论了通过质谱流程取得的几个生物学发现,重点是细胞信号蛋白质组学。