Fröhlich T, Arnold G J
Laboratory for Functional Genome Analysis (LAFUGA), Gene Center, Ludwig-Maximilians University Munich, Germany.
J Neural Transm (Vienna). 2006 Aug;113(8):973-94. doi: 10.1007/s00702-006-0509-3. Epub 2006 Jul 13.
Recent developments of new generations of mass spectrometers and improvements in the field of chromatography have revolutionized protein analytics. Particularly the combination of liquid chromatography as a separation tool for proteins and peptides with tandem mass spectrometry as an identification tool referred to as LC-MS/MS has generated a powerful and broadly used technique in the field of proteomics. The resolution and sensitivity of state-of-the-art LC-MS/MS systems has reached dimensions allowing not only the analysis of individual proteins but also investigations on the level of complete proteomes. However, the enormous complexity and the extreme concentration range of proteins within typical eukaryotic proteomes are still the major challenge of this technique. This review gives an overview of modern LC-MS/MS based proteomics, describing state-of-the-art chromatography and modern mass spectrometry. Strategies to perform quantitative proteomics will be presented and capabilities as well as current limitations of this innovative methodology will be discussed.
新一代质谱仪的最新进展以及色谱领域的改进彻底改变了蛋白质分析方法。特别是液相色谱作为蛋白质和肽的分离工具与串联质谱作为鉴定工具相结合,即所谓的LC-MS/MS,已在蛋白质组学领域产生了一种强大且广泛应用的技术。最先进的LC-MS/MS系统的分辨率和灵敏度已达到不仅能够分析单个蛋白质,还能对完整蛋白质组水平进行研究的程度。然而,典型真核生物蛋白质组中蛋白质的巨大复杂性和极端浓度范围仍然是该技术的主要挑战。本综述概述了基于现代LC-MS/MS的蛋白质组学,描述了最先进的色谱法和现代质谱法。将介绍进行定量蛋白质组学的策略,并讨论这种创新方法的能力以及当前的局限性。