Kumar Sunil, Punekar Narayan S
Biotechnology Group, Department of Biosciences and Bioengineering, Indian Institute of Technology Bombay, Mumbai, India.
Methods Mol Biol. 2014;1129:53-65. doi: 10.1007/978-1-62703-977-2_6.
Dye-ligand-based chromatography has become popular after Cibacron Blue, the first reactive textile dye, found application for protein purification. Many other textile dyes have since been successfully used to purify a number of proteins and enzymes. While the exact nature of their interaction with target proteins is often unclear, dye-ligands are thought to mimic the structural features of their corresponding substrates, cofactors, etc. The dye-ligand affinity matrices are therefore considered pseudo-affinity matrices. In addition, dye-ligands may simply bind with proteins due to electrostatic, hydrophobic, and hydrogen-bonding interactions. Because of their low cost, ready availability, and structural stability, dye-ligand affinity matrices have gained much popularity. Choice of a large number of dye structures offers a range of matrices to be prepared and tested. When presented in the high-throughput screening mode, these dye-ligand matrices provide a formidable tool for protein purification. One could pick from the list of dye-ligands already available or build a systematic library of such structures for use. A high-throughput screen may be set up to choose best dye-ligand matrix as well as ideal conditions for binding and elution, for a given protein. The mode of operation could be either manual or automated. The technology is available to test the performance of dye-ligand matrices in small volumes in an automated liquid-handling workstation. Screening a systematic library of dye-ligand structures can help establish a structure-activity relationship. While the origins of dye-ligand chromatography lay in exploiting pseudo-affinity, it is now possible to design very specific biomimetic dye structures. High-throughput screening will be of value in this endeavor as well.
自从第一种活性纺织染料汽巴蓝被用于蛋白质纯化后,基于染料配体的色谱法开始流行起来。此后,许多其他纺织染料也成功用于纯化多种蛋白质和酶。虽然它们与目标蛋白质相互作用的确切性质往往尚不清楚,但染料配体被认为能够模拟其相应底物、辅因子等的结构特征。因此,染料配体亲和基质被视为假亲和基质。此外,染料配体可能仅因静电、疏水和氢键相互作用而与蛋白质结合。由于成本低、易于获得且结构稳定,染料配体亲和基质广受欢迎。大量染料结构可供选择,这使得一系列基质得以制备和测试。当以高通量筛选模式呈现时,这些染料配体基质为蛋白质纯化提供了一个强大的工具。人们可以从现有的染料配体列表中挑选,也可以构建这样的结构系统库以供使用。可以设置高通量筛选来为给定蛋白质选择最佳的染料配体基质以及理想的结合和洗脱条件。操作模式可以是手动的,也可以是自动的。该技术可用于在自动液体处理工作站中以小体积测试染料配体基质的性能。筛选染料配体结构的系统库有助于建立构效关系。虽然染料配体色谱法起源于利用假亲和性,但现在有可能设计出非常特异的仿生染料结构。高通量筛选在这一努力中也将具有价值。