Ion exchange chromatography of proteins—prediction of elution curves and operating conditions. I. Theoretical considerations
- 1 June 1983
- journal article
- research article
- Published by Wiley in Biotechnology & Bioengineering
- Vol. 25 (6), 1465-1483
- https://doi.org/10.1002/bit.260250605
Abstract
A mathematical model is proposed for the elution of proteins on ion exchange columns by a linear gradient increase and stepwise increase of ionic strength in order to predict relationships between the elution characteristics (the peak position, the peak width, etc.) and the operating conditions (the flow rate, the slope of gradient, etc). This model is in principle based on the continuous‐flow plate theory, in which the protein concentration and ionic strength dependent distibution coefficient between proteins and ion exchangers and zone sperading effects are taken into consideration. The advantage of this model is its simplicity since it requires only two parameters: The distribution coefficient and the number of plates. Since the distribution coefficient of proteins depends on both the protein concentration and ionic strength of the elution buffer, the number of plates should vary with time. However, it is extremely difficult to take into consideration the time‐dependent number of plates. Therefore, we assume that the number of plates is constant and related to that number derived from a mass balance model which includes longitudinal dispersion and gel phase diffusion. On the basis of these assumptions, a method for determining the number of plates by the moment method is presented. Although the dependencies of the peak position and peak width on the slope of linear gradient are predictable by numerical calculations of the present model, simpler methods for prediction of these dependencies are desirable. A graphical method is proposed for prediction of the peak position. For prediction of the peak width, an asymptotic solution is derived from a quasi‐steady‐state model.This publication has 30 references indexed in Scilit:
- Ion exchange chromatography of proteins—predictions of elution curves and operating conditions. II. Experimental verificationBiotechnology & Bioengineering, 1983
- Analysis of dispersion mechanism in gel chromatography. IV. Operational conditions for gel chromatography - Prediction of elution curves.Agricultural and Biological Chemistry, 1979
- Continuous Flow Equilibrium Staged Model for Cycling Zone AdsorptionIndustrial & Engineering Chemistry Fundamentals, 1978
- Kinetics of glucoamylase immobilized by ionic linkage and analysis of its adsorption and desorption processes.Agricultural and Biological Chemistry, 1978
- Analysis of dispersion mechanism in gel chromatography.Agricultural and Biological Chemistry, 1977
- Moment analysis of experiments in gel permeation chromatographyAIChE Journal, 1973
- Chromatography of proteins and peptides on sephadex ion‐exchangers: Dependence of the resolution on the elution scheduleFEBS Letters, 1971
- Investigations on the resolving power of hydroxyapatite columnsBiopolymers, 1970
- Ion Exchange as a Separations Method. IX. Gradient Elution Theory1Journal of the American Chemical Society, 1955
- The Theory of ChromatographyJournal of the American Chemical Society, 1943