Sadakane Yutaka, Hatanaka Yasumaru
Faculty of Pharmaceutical Sciences, Kyushu University of Health and Welfare, 1714-1 Yoshino-cho, Nobeoka 882-8508, Japan.
Anal Sci. 2006 Feb;22(2):209-18. doi: 10.2116/analsci.22.209.
Photoaffinity labeling enables the direct probing of a target protein through a covalent bond between a ligand and its binding protein, and even a complex formed by weak interactions can be isolated by the method. The photochemical fishing approach accelerates the throughput, isolating crosslinked complexes and analyzing the structure of the ligand binding site within the protein. We used carbene-generating phenyldiazirine for this approach because practical examinations had shown that the phenyldiazirine functioned as the powerful barb on the hook. Improving the synthetic pathways of the photoprobes and using chemoselective-integrated photoreactive units makes possible the easy and rapid preparation of carbene-generating photoreactive probes including the derivatives in peptides, proteins, DNAs, and carbohydrates. This review also shows several recent impacts of photoaffinity labeling, including the in vivo preparation of photoreactive proteins in living cells.
光亲和标记能够通过配体与其结合蛋白之间的共价键直接探测目标蛋白,甚至通过该方法可以分离由弱相互作用形成的复合物。光化学筛选方法提高了通量,可分离交联复合物并分析蛋白质内配体结合位点的结构。我们使用产生卡宾的苯基重氮甲烷进行该方法,因为实际测试表明苯基重氮甲烷在该过程中发挥着强力鱼钩倒刺的作用。改进光探针的合成途径并使用化学选择性整合的光反应单元,使得能够轻松快速地制备包括肽、蛋白质、DNA和碳水化合物衍生物在内的产生卡宾的光反应探针。本综述还展示了光亲和标记最近的一些影响,包括在活细胞中体内制备光反应性蛋白质。