Abstract
The free solution electrophoretic mobility of DNA differs significantly in different buffers, suggesting that DNA-buffer interactions are present in certain buffer systems. Here, capillary and gel electrophoresis data are combined to show that the Tris ions in Tris-acetate-EDTA (TAE) buffers are associated with the DNA helix to approximately the same extent as sodium ions. The borate ions in Tris-borate-EDTA (TBE) buffers interact with DNA to form highly charged DNA-borate complexes, which are stable both in free solution and in polyacrylamide gels. DNA-borate complexes are not observed in agarose gels, because of the competition of the agarose gel fibers for the borate residues. The resulting agarose-borate complexes increase the negative charge of the agarose gel fibers, leading to an increased electroendosmotic flow of the solvent in agarose-TBE gels. The combined results indicate that the buffers in which DNA is studied cannot automatically be assumed to be innocuous. (C) 2000 John Wiley and Sons, Inc.
Original language | English |
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Pages (from-to) | 137-142 |
Number of pages | 6 |
Journal | Biopolymers |
Volume | 54 |
Issue number | 2 |
DOIs | |
Publication status | Published - 2000 |
Keywords
- Agarose gels
- DNA
- DNA capillary electrophoresis
- DNA gel electrophoresis
- DNA-borate complexes
- Electroendosmotic flow
ASJC Scopus subject areas
- Biochemistry, Genetics and Molecular Biology(all)
- Biochemistry
- Biophysics