Recent advances in 2D electrophoresis: an array of possibilities

被引:39
作者
Van den Bergh, G [1 ]
Arckens, L [1 ]
机构
[1] Katholieke Univ Leuven, Dept Biol, Lab Neuroplast & Neuroproteom, B-3000 Louvain, Belgium
关键词
2D-DIGE; 2D-PAGE; fluorescence; functional proteomics; glycosylation; isotope-coded 2D maps; phophorylation; ProQ diamond; ProQ emerald; protein prefractionation;
D O I
10.1586/14789450.2.2.243
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
2D electrophoresis is currently the most widespread technique used for performing functional proteomics (i.e., the large-scale analysis of alterations in protein expression levels). Nevertheless, several limitations inherent to this technology have restricted the full potential of this protein differential display methodology for years. This has even led to the abandonment of 2D electrophoresis by several groups that switched to performing gel-free functional proteomics analyses based on liquid chromatography and mass spectrometry. Meanwhile, important recent advances in 2D electrophoresis, such as the introduction of fluorescent 2D difference gel electrophoresis and numerous protein prefractionation techniques, have thoroughly modernized 2D electrophoresis, making it again one of the preferred methods for the analysis of protein expression differences in many laboratories.
引用
收藏
页码:243 / 252
页数:10
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