4.7 Article

Preparation of phenylboronic acid functionalized cation-exchange monolithic columns for protein separation and refolding

Journal

TALANTA
Volume 81, Issue 3, Pages 856-864

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.talanta.2010.01.029

Keywords

Surface functionalization; Phenylboronic acid; Cation-exchange chromatography; Protein separation; Refolding

Funding

  1. National Basic Research Program of China [2007CB914100]
  2. 863 program [2007AA10Z432, 2006AA10Z438]
  3. National Natural Science Foundation of China [20935001, 20675040, 20875050]

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In this study, we described a simple and effective modification procedure to prepare poly (methacrylate-co-ethylene glycol dimethacrylate) monolithic columns functionalized with 3-aminophenylboronic acid. The column morphology, pore size and specific surface area of the fabricated monolith were characterized by scanning electron microscopy, X-ray photoelectron spectroscopy, thermogravimetric analysis, and mercury intrusion porosimeter, respectively. The frontal analysis was carried out for dynamic loading capacity of the model protein on the modified column. The chromatographic performance of the cation-exchange monolith was evaluated through separating a mixture of five proteins such as lysozyme, cytochrome c, ribonuclease A, trypsin and bovine serum albumin and one-step purification of lysozyme from egg whites, and the expected results were obtained. In addition, the functionalized column was used to refold ribonuclease A and cytochrome c. and this procedure was monitored by circular dichroism and fluorescence spectroscopy. Compared with the conventional dilution refolding method, the ion-exchange chromatography refolding method developed here is more effective for specific bioactivity recovery. (C) 2010 Elsevier B.V. All rights reserved.

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