Tris(hydroxymethyl)aminomethane-functionalized agarose particles: parameters affecting the binding of bovine serum albumin

J Sep Sci. 2012 Jun;35(12):1406-10. doi: 10.1002/jssc.201200118.

Abstract

A new protein adsorbent is introduced based on the coupling of the common buffer ion, tris(hydroxymethyl)aminomethane, to the agarose gel Sepharose HP from GE Healthcare Bio-Sciences AB, Uppsala, Sweden. The article describes the synthesis of the new adsorbent and the use of BSA as a model in a binding study. By optimization of the coupling procedure, a maximum ligand density of 63.5 μmol/mL gel could be obtained. Adsorption equilibria were investigated in the pH range 5.0-8.0 and at salt concentrations of 0-0.4 mol/L. Binding of BSA under different conditions indicated that both electrostatic interaction and hydrogen bonding were involved in the adsorption process where the former played a major role.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adsorption
  • Animals
  • Cattle
  • Chromatography, Gel / instrumentation*
  • Chromatography, Gel / methods
  • Kinetics
  • Protein Binding
  • Sepharose / chemistry
  • Serum Albumin, Bovine / chemistry
  • Serum Albumin, Bovine / isolation & purification*
  • Tromethamine / chemistry*

Substances

  • Tromethamine
  • Serum Albumin, Bovine
  • Sepharose