Phillips Carolyn I, Bogyo Matthew
Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, CA 94305-5324, USA.
Cell Microbiol. 2005 Aug;7(8):1061-76. doi: 10.1111/j.1462-5822.2005.00554.x.
The availability of complete genome sequences for a large number of pathogenic organisms has opened the door for large-scale proteomic studies to dissect both protein expression/regulation and function. This review highlights key proteomic methods including two-dimensional gel electrophoresis, reference mapping, protein expression profiling and recent advances in gel-free separation techniques that have made a significant impact on the resolution of complex proteomes. In addition, we highlight recent developments in the field of chemical proteomics, a branch of proteomics aimed at functionally profiling a proteome. These techniques include the development of activity-based probes and activity-based protein profiling methods as well as the use of synthetic small molecule libraries to screen for pharmacological tools to perturb basic biological processes. This review will focus on the applications of these technologies to the field of microbiology.
大量致病生物全基因组序列的可得性,为大规模蛋白质组学研究打开了大门,以剖析蛋白质表达/调控及功能。本综述重点介绍了关键的蛋白质组学方法,包括二维凝胶电泳、参考图谱绘制、蛋白质表达谱分析,以及无凝胶分离技术的最新进展,这些进展对复杂蛋白质组的分辨率产生了重大影响。此外,我们还重点介绍了化学蛋白质组学领域的最新发展,化学蛋白质组学是蛋白质组学的一个分支,旨在对蛋白质组进行功能分析。这些技术包括基于活性的探针和基于活性的蛋白质谱分析方法的开发,以及使用合成小分子文库筛选干扰基本生物学过程的药理学工具。本综述将聚焦于这些技术在微生物学领域的应用。