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Molecular Sieving of Polystyrene Carboxylate of a Diameter up to 10 μm in Solutions of Uncrosslinked Polyacrylamide of Mr 5 × 106 Using Capillary Zone Electrophoresis

✍ Scribed by S.P. Radko; M.M. Garner; G. Caiafa; A. Chrambach


Publisher
Elsevier Science
Year
1994
Tongue
English
Weight
448 KB
Volume
223
Category
Article
ISSN
0003-2697

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✦ Synopsis


Capillary zone electrophoresis of polystyrene carboxylate (PSC) up to (10 \mu \mathrm{m}) in diameter in 0.1 to (0.9 %) solutions of uncrosslinked polyacrylamide (PA) of (M_{\mathrm{r}} 5) (\times 10^{6}) demonstrates effective molecular sieving in that medium. The reduced mobility, however, is not constant in Tris-borate-EDTA ( (1 \times) TBE) buffer containing the polymer but increases in proportion to the load of PSC and inversely to the concentration of PA unless the TBE concentration is increased 10 -fold or (50 \mathrm{~mm} 3-) [(3-cholamidopropyl)dimethylammonio]propanesulfonic acid is added to the solution or in the absence of PA. Both the Ferguson plots ([\log () mobility) vs PA concentration] of PSC obtained at various PSC loads and the effects of the dissociating conditions, high ionic strength and detergent, signify that the variable mobilities are those of different PSC aggregation states. Thus, only the fully associated or dissociated states of PSC provide mobilities that are constant independently of PSC load. The study shows that the information inherent in Ferguson plots regarding particle and fiber properties can be exploited for particles up to (10 \mu \mathrm{m}) in diameter by capillary zone electrophoresis in polymer solutions even if these particles form various aggregation states. Thus, such an analysis appears feasible in application to biologically relevant and functional complexes such as subcellular-sized particles or DNA-protein complexes, providing that these particles maintain their integrity and functionality under the selected electrophoretic conditions. 1994 Academic Press, Inc.