Immobilized pH gradient

General Structure of Immobiline. ^[1]

Immobilized pH gradient (IPG) gels are the acrylamide gel matrix co-polymerized with the pH gradient, which result in completely stable gradients except the most alkaline (>12) pH values. The immobilized pH gradient is obtained by the continuous change in the ratio of Immobilines. An Immobiline is a weak acid or base defined by its pK value.^[2] Immobilized pH gradients (IPG) are made by mixing two kinds of acrylamide mixure, one with Immobiline having acidic buffering property and other with basic buffering property.^[3] The concentrations of the buffers in the two solutions define the range and shape of the pH gradient produced. Both solutions contain acrylamide monomers and catalysts. During polymerization, the acrylamide portion of the buffers co polymerize with the acrylamide and bisacrylamide monomers to form a polyacrylamide gel. These polymerised gels are backed with plastic based backing that allow ease in handling and improve IPG's performance. The gel is then washed to remove catalysts and unpolymerized monomers, which interfere with isoelectric separation. IPG increased reproducibility^[4][5] of Isoelectric focusing and 2D-Gel Electrophoresis. Other advantages are increased resolution,^[6] reproducible separation of alkaline proteins^[7] and increased loading capacity (up to 10 mg).^[8]

This alternative method eliminates the problems of gradient instability and poor sample loading capacity associated with carrier ampholyte pH gradient.^[9] Commercial precast IPG gels are available.

References

1. ↑ Görg, Angelika; Weiss, Walter; Dunn, Michael J. (2004-12-01). "Current two-dimensional electrophoresis technology for proteomics". Proteomics. 4 (12): 3665–3685. doi:10.1002/pmic.200401031. ISSN 1615-9853. PMID 15543535. 
2. ↑ Barnes et al., Electrophoresis in Practice: A Guide to theory and Practice. Page 44. VCH Publishers Inc, 1993 (USA)
3. ↑ Görg, Angelika; Weiss, Walter; Dunn, Michael J. (2004-12-01). "Current two-dimensional electrophoresis technology for proteomics". Proteomics. 4 (12): 3665–3685. doi:10.1002/pmic.200401031. ISSN 1615-9853. PMID 15543535. 
4. ↑ Corbett, J. M.; Dunn, M. J.; Posch, A.; Görg, A. (1994-09-01). "Positional reproducibility of protein spots in two-dimensional polyacrylamide gel electrophoresis using immobilised pH gradient isoelectric focusing in the first dimension: an interlaboratory comparison". Electrophoresis. 15 (8-9): 1205–1211. ISSN 0173-0835. PMID 7532129. 
5. ↑ Blomberg, A.; Blomberg, L.; Norbeck, J.; Fey, S. J.; Larsen, P. M.; Larsen, M.; Roepstorff, P.; Degand, H.; Boutry, M. (1995-10-01). "Interlaboratory reproducibility of yeast protein patterns analyzed by immobilized pH gradient two-dimensional gel electrophoresis". Electrophoresis. 16 (10): 1935–1945. ISSN 0173-0835. PMID 8586069. 
6. ↑ Wildgruber, R.; Harder, A.; Obermaier, C.; Boguth, G.; Weiss, W.; Fey, S. J.; Larsen, P. M.; Görg, A. (2000-07-01). "Towards higher resolution: two-dimensional electrophoresis of Saccharomyces cerevisiae proteins using overlapping narrow immobilized pH gradients". Electrophoresis. 21 (13): 2610–2616. doi:10.1002/1522-2683(20000701)21:13<2610::AID-ELPS2610>3.0.CO;2-H. ISSN 0173-0835. PMID 10949137. 
7. ↑ Wildgruber, Robert; Reil, Gerold; Drews, Oliver; Parlar, Harun; Görg, Angelika (2002-06-01). "Web-based two-dimensional database of Saccharomyces cerevisiae proteins using immobilized pH gradients from pH 6 to pH 12 and matrix-assisted laser desorption/ionization-time of flight mass spectrometry". Proteomics. 2 (6): 727–732. doi:10.1002/1615-9861(200206)2:6<727::AID-PROT727>3.0.CO;2-2. ISSN 1615-9853. PMID 12112855. 
8. ↑ Görg, A.; Postel, W.; Friedrich, C.; Kuick, R.; Strahler, J. R.; Hanash, S. M. (1991-09-01). "Temperature-dependent spot positional variability in two-dimensional polypeptide patterns". Electrophoresis. 12 (9): 653–658. doi:10.1002/elps.1150120910. ISSN 0173-0835. PMID 1752246. 
9. ↑ Wilkins et al., Proteome Research: New Frontiers in Functional Genomics. Page 14. Springer, 1997 (Germany)