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Determining the electrophoretic mobility and translational diffusion coefficients of DNA molecules in free solution
Author(s) -
Stellwagen Earle,
Stellwagen Nancy C.
Publication year - 2002
Publication title -
electrophoresis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.666
H-Index - 158
eISSN - 1522-2683
pISSN - 0173-0835
DOI - 10.1002/1522-2683(200208)23:16<2794::aid-elps2794>3.0.co;2-y
Subject(s) - chemistry , dna , diffusion , electrophoresis , molecule , counterion , persistence length , capillary electrophoresis , analytical chemistry (journal) , base pair , chromatography , biophysics , ion , biochemistry , organic chemistry , biology , thermodynamics , physics
The free solution mobility of DNA molecules of different molecular weights, the sequence dependence of the mobility, and the diffusion coefficients of small single‐ and double‐stranded DNA (ss‐ and dsDNA) molecules can be measured accurately by capillary zone electrophoresis, using coated capillaries to minimize the electroosmotic flow (EOF) of the solvent. Very small differences in mobility between various analytes can be quantified if a mobility marker is used to correct for small differences in EOF between successive experiments. Using mobility markers, the molecular weight at which the free solution mobility of dsDNA becomes independent of molecular weight is found to be ∼ 170 bp in 40 m M Tris‐acetate‐EDTA buffer. A DNA fragment containing 170 bp has a contour length of ∼ 58 nm, close to the persistence length of DNA under these buffer conditions. Hence, the approach of the free solution mobility of DNA to a plateau value may be associated with the transition from a rod‐like to a coil‐like conformation in solution. Markers have also been used to determine that the free solution mobilities of ss‐ and dsDNA oligomers are sequence‐dependent. Double‐stranded 20‐bp oligomers containing runs of three or more adenine residues in a row (A‐tracts) migrate somewhat more slowly than 20‐mers without A‐tracts, suggesting that somewhat larger numbers of counterions are condensed in the ion atmospheres of A‐tract DNAs, decreasing their net effective charge. Single‐stranded 20‐mers with symmetric sequences migrate ∼ 1% faster than their double‐stranded counterparts, and faster than single‐stranded 20‐mers containing A 5 ‐ or T 5 ‐tracts. Interestingly, the average mobility of two complementary single‐stranded 20‐mers is equal to the mobility of the double‐stranded oligomer formed upon annealing. Finally, the stopped migration method has been used to measure the diffusion coefficients of single‐ and double‐stranded oligomers. The diffusion coefficients of ssDNA oligomers containing 20 nucleotides are ∼ 50% larger than those of double‐stranded DNA oligomers of the same size, reflecting the greater flexibility of ssDNA molecules. The methods used to carry out these experiments are also described in detail.