Sorption Effects in Gel Filtration: I. A Survey of Amino Acid Behavior on Sephadex G-10
- 1 January 1967
- journal article
- research article
- Published by Taylor & Francis in Separation Science
- Vol. 2 (4) , 507-550
- https://doi.org/10.1080/01496396708049718
Abstract
Sephadex G-10, as supplied by the manufacturer, behaves as a weak cation exchanger. The cation-exchange capacity can be nearly eliminated by washing the gel with 1 M aqueous pyridine. The behavior of amino acids and other small solutes on pyridine-washed columns under defined conditions is very reproducible. The behavior of a solute on Sephadex G-10 fundamentally depends on its effective molecular size. Charged solutes tend to be excluded in media of low ionic strength, but the effective size and hence the degree of exclusion of such molecules can be decreased substantially by including high concentrations of small electrolytes in the medium. Salt can increase the adsorption of potentially adsorbable charged molecules in a passive way by increasing the amount of gel available to them. Salt might actively promote the adsorption of hydrophobic molecules by causing them to seek out regions within the gel where there is no salt, e.g., in the immediate vicinity of the gel matrix. Any pair of small water-soluble molecules that differ with respect to size, charge, content of delocalized π electrons, or hydrophobic character (e.g., the length of a linear hydrocarbon chain) should be separable on Sephadex G-10. The gel should therefore be very useful for purifying small water-soluble synthetic products.Keywords
This publication has 19 references indexed in Scilit:
- Determination of molecular weights and frictional ratios of proteins in impure systems by use of gel filtration and density gradient centrifugation. Application to crude preparations of sulfite and hydroxylamine reductasesPublished by Elsevier ,2003
- The correlation between molecular weight and elution behaviour in the gel chromatography of proteinsJournal of Chromatography A, 1966
- Molecular-Sieve Chromatography of Proteins on Granulated Polyacrylamide GelsSeparation Science, 1966
- SOLUTE BEHAVIOR IN TIGHTLY CROSS‐LINKED DEXTRAN GELSAnnals of the New York Academy of Sciences, 1965
- THE EFFECT OF SOLUTES ON THE STRUCTURE OF WATER AND ITS IMPLICATIONS FOR PROTEIN STRUCTURE*Annals of the New York Academy of Sciences, 1965
- Handbook of analytical chemistry : Edited by L. Meites, McGraw-Hill Book Company, Inc., New York, 1963, price £ 18.8.0.Journal of Chromatography A, 1964
- Propriétés échangeuses d'ions du gel de dextrane (sephadex): Application à la mise au point d'une technique de rétention réversible des protéines basiques de faible poids moléculaireJournal of Chromatography A, 1962
- The fractionation of histones on Sephadex G-75Biochimica et Biophysica Acta, 1961
- Studies on gel filtration : Sorption properties of the bed material sephadexJournal of Chromatography A, 1960
- Gel Filtration: A Method for Desalting and Group SeparationNature, 1959