Laboratory of Enzyme Technology, Department of Biotechnology, School of Applied Biology and Biotechnology, Agricultural University of Athens, Athens, Greece.
Methods Mol Biol. 2021;2178:201-215. doi: 10.1007/978-1-0716-0775-6_15.
Dye-ligand affinity chromatography is a widely used technique in protein purification. The utility of the reactive dyes as affinity ligands results from their unique chemistry, which confers wide specificity toward a large number of proteins. They are commercially available, inexpensive, stable and can easily be immobilized. Significant factors that contribute to the successful operation of a dye-ligand chromatography include matrix type, dye-ligand density, adsorption along with elution conditions and flow rate. The present chapter provides protocols for the synthesis of dye-ligand affinity adsorbents as well as protocols for screening, selection, and optimization of a given dye-ligand purification step. The purification of the glutathione transferases from Phaseolus vulgaris on Cibacron Blue 3GA-Sepharose affinity adsorbent is given as an example.
染料配体亲和层析是一种广泛应用于蛋白质纯化的技术。反应染料作为亲和配体的应用源于其独特的化学性质,使其对大量蛋白质具有广泛的特异性。它们是商业上可获得的、廉价的、稳定的,并且可以很容易地固定化。有助于染料配体层析成功运行的重要因素包括基质类型、染料配体密度、吸附以及洗脱条件和流速。本章提供了合成染料配体亲和吸附剂的方案,以及筛选、选择和优化给定染料配体纯化步骤的方案。以 Cibacron Blue 3GA-Sepharose 亲和吸附剂从菜豆中纯化谷胱甘肽转移酶为例。