Ferguson P Lee, Smith Richard D
Biological Sciences Division, Pacific Northwest National Laboratory, Richland, Washington 99352, USA.
Annu Rev Biophys Biomol Struct. 2003;32:399-424. doi: 10.1146/annurev.biophys.32.110601.141854. Epub 2003 Jan 28.
The coupling of high-performance mass spectrometry instrumentation with highly efficient chromatographic and electrophoretic separations has enabled rapid qualitative and quantitative analysis of thousands of proteins from minute samples of biological materials. Here, we review recent progress in the development and application of mass spectrometry-based techniques for the qualitative and quantitative analysis of global proteome samples derived from whole cells, tissues, or organisms. Techniques such as multidimensional peptide and protein separations coupled with mass spectrometry, accurate mass measurement of peptides from global proteome digests, and mass spectrometric characterization of intact proteins hold great promise for characterization of highly complex protein mixtures. Advances in chemical tagging and isotope labeling techniques have enabled quantitative analysis of proteomes, and highly specific isolation strategies have been developed aimed at selective analysis of posttranslationally modified proteins.
高性能质谱仪器与高效色谱及电泳分离技术的联用,已能够对来自微量生物材料样本中的数千种蛋白质进行快速定性和定量分析。在此,我们综述了基于质谱技术在全细胞、组织或生物体来源的整体蛋白质组样本定性和定量分析方面的最新进展。诸如多维肽和蛋白质分离与质谱联用、对整体蛋白质组消化产生的肽段进行精确质量测量以及对完整蛋白质进行质谱表征等技术,在表征高度复杂的蛋白质混合物方面具有巨大潜力。化学标记和同位素标记技术的进展已实现对蛋白质组的定量分析,并且已开发出高度特异性的分离策略,旨在对翻译后修饰的蛋白质进行选择性分析。