Two-dimensional gel electrophoresis in proteomics: past, present and future
arXiv:1008.2591 · doi:10.1016/j.jprot.2010.05.016
Abstract
Two-dimensional gel electrophoresis has been instrumental in the birth and developments of proteomics, although it is no longer the exclusive separation tool used in the field of proteomics. In this review, a historical perspective is made, starting from the days where two-dimensional gels were used and the word proteomics did not even exist. The events that have led to the birth of proteomics are also recalled, ending with a description of the now well-known limitations of two-dimensional gels in proteomics. However, the often-underestimated advantages of two-dimensional gels are also underlined, leading to a description of how and when to use two-dimensional gels for the best in a proteomics approach. Taking support of these advantages (robustness, resolution, and ability to separate entire, intact proteins), possible future applications of this technique in proteomics are also mentioned.
References in corpus (12)
- Silver staining of proteins in polyacrylamide gels
- Improvement of the solubilization of proteins in two-dimensional electrophoresis with immobilized pH gradients
- Evaluation of nonionic and zwitterionic detergents as membrane protein solubilizers in two-dimensional electrophoresis
- Guidelines for the next 10 years of proteomics
- Membrane proteins and proteomics: Love is possible, but so difficult
- How shall we use the proteomics toolbox for biomarker discovery?
- Power and limitations of electrophoretic separations in proteomics strategies
- Progress in the definition of a reference human mitochondrial proteome
- About the mechanism of interference of silver staining with peptide mass spectrometry
- Sweet silver: A formaldehyde-free silver staining using aldoses as developing agents, with enhanced compatibility with mass spectrometry
- Alterations of the mitochondrial proteome caused by the absence of mitochondrial DNA: A proteomic view
- Ultrafast coelectrophoretic fluorescent staining of proteins with carbocyanines