Central Clinical School, Department of Neurology, University of Sydney, Sydney, NSW, Australia.
Proteomics. 2011 Feb;11(4):513-34. doi: 10.1002/pmic.201000394. Epub 2011 Jan 17.
The identification, quantitation and global characterisation of all proteins within a given proteome are extremely challenging. This is due to the absolute detection limits of technology as well as the dynamic range in expression of proteins; and the extreme diversity and heterogeneity of the proteome. To overcome such issues, the use of separation technologies has played a critical role in reducing sample complexity. To date, a plethora of chromatographic and electrophoretic fractionation tools have evolved over the years assisting in simplifying complex protein and peptide mixtures. Here, we review a range of these technologies highlighting the challenges of protein and peptide analysis in the context of proteome research and some of the advantages and disadvantages of present techniques.
在给定的蛋白质组中鉴定、定量和全面描述所有蛋白质极具挑战性。这是由于技术的绝对检测限以及蛋白质表达的动态范围;以及蛋白质组的极端多样性和异质性。为了克服这些问题,分离技术的使用在降低样品复杂性方面发挥了关键作用。迄今为止,多年来已经开发出了大量的色谱和电泳分离工具,有助于简化复杂的蛋白质和肽混合物。在这里,我们回顾了其中的一些技术,强调了蛋白质组研究中蛋白质和肽分析的挑战,以及现有技术的一些优点和缺点。