Kaneda Masaki, Sadakane Yutaka, Hatanaka Yasumaru
Faculty of Pharmaceutical Sciences, Toyama Medical and Pharmaceutical University, 2630 Sugitani, Toyama 930-0194, Japan.
Bioconjug Chem. 2003 Sep-Oct;14(5):849-52. doi: 10.1021/bc0340520.
A novel application of the photoaffinity technique has been developed for the efficient discovery of small ligand and macromolecule interaction. The approach, photoaffinity capture, uses a photoreactive protein together with immobilized ligand for the rapid screening of competitive inhibitors. The set of photoreactive glyceraldehyde-3-phosphate dehydrogenase (photo-GAPDH) and immobilized dye ligand was prepared and examined as a model system. The photo-GAPDH was shown to efficiently capture the immobilized ligand. When nonimmobilized competitive ligands were included in the system, the capture was prevented in accordance with the affinity of the ligands. The present approach would provide an efficient tool for affinity-based screening of ligand libraries.
一种用于高效发现小分子配体与大分子相互作用的光亲和技术新应用已被开发出来。这种方法,即光亲和捕获,使用一种光反应性蛋白质和固定化配体来快速筛选竞争性抑制剂。制备了光反应性甘油醛-3-磷酸脱氢酶(光-GAPDH)和固定化染料配体的组合,并将其作为模型系统进行研究。结果表明,光-GAPDH能够有效地捕获固定化配体。当系统中加入非固定化的竞争性配体时,捕获作用会根据配体的亲和力而受到抑制。本方法将为基于亲和力的配体库筛选提供一种有效的工具。