Mitulovic Goran, Mechtler Karl
Research Institute of Molecular Pathology, Dr. Bohrgasse 7, A-1030 Wien, Austria.
Brief Funct Genomic Proteomic. 2006 Dec;5(4):249-60. doi: 10.1093/bfgp/ell034. Epub 2006 Nov 22.
Due to the complex nature of the proteome, instrumentation and methods development for sample cleanup, fractionation, preconcentration, chromatographic separation and detection becomes urgent for the identification of peptides and proteins. Newly developed techniques and equipment for separation and detection, such as nano-HPLC and multidimensional HPLC for protein and peptide separation, enabled proteomics to experience dynamic growth during the past few years. In any proteomic analysis the most important and sometimes most difficult task is the separation of the complex mixture of proteins or peptides. This review describes some aspects and limitations of HPLC, both multidimensional and one-dimensional, in proteomics research without attempting to discuss all available HPLC methods, which would need far more space than available here.
由于蛋白质组的复杂性,用于样品净化、分级分离、预浓缩、色谱分离和检测的仪器及方法开发对于肽和蛋白质的鉴定变得十分迫切。新开发的分离和检测技术与设备,如用于蛋白质和肽分离的纳米高效液相色谱(nano-HPLC)和多维高效液相色谱,使得蛋白质组学在过去几年中得到了蓬勃发展。在任何蛋白质组学分析中,最重要且有时最困难的任务是分离蛋白质或肽的复杂混合物。本综述描述了多维和一维高效液相色谱在蛋白质组学研究中的一些方面及局限性,而不试图讨论所有可用的高效液相色谱方法,因为这需要比此处更多的篇幅。