Guo Haijun, Li Zhengqiu
College of Pharmacy , Jinan University , Guangzhou , 510632 China . Email:
Medchemcomm. 2017 Jun 14;8(8):1585-1591. doi: 10.1039/c7md00217c. eCollection 2017 Aug 1.
Photoaffinity labeling (PAL) has been widely applied in various research areas such as medicinal chemistry, chemical biology and structural biology, owing to its capability of investigating non-covalent ligand-protein interactions under native environments and elucidating protein structures, functions One important application of this technique is to use affinity-based proteome profiling (ABP) coupled with bioimaging for profiling drug-target interactions . In order to accurately report drug-target interactions these approaches, several considerations as follows need to be made: (1) maximally retaining bioactivities of photoprobes upon functionalization with a photoreactive group and a reporter tag from a parental compound; (2) performing proteome profiling and imaging simultaneously, to monitor drug-target interactions in different manners; and (3) developing excellent photo-crosslinkers capable of photo-crosslinking and fluorescence turn-on at the same time. With these considerations in mind, we have developed three versions of "minimalist" bioorthogonal handle-containing photo-crosslinkers (L3-L6) during the years and successfully applied them in all kinds of small bioactive molecules for protein labeling and cellular imaging studies. In this mini-review, the features and functions of these linkers are specifically highlighted and summarized.
光亲和标记(PAL)因其能够在天然环境下研究非共价配体-蛋白质相互作用并阐明蛋白质结构和功能,已在药物化学、化学生物学和结构生物学等多个研究领域得到广泛应用。该技术的一个重要应用是将基于亲和力的蛋白质组分析(ABP)与生物成像相结合,用于分析药物-靶点相互作用。为了通过这些方法准确报告药物-靶点相互作用,需要考虑以下几点:(1)在用光反应基团和来自母体化合物的报告标签进行功能化时,最大程度地保留光探针的生物活性;(2)同时进行蛋白质组分析和成像,以不同方式监测药物-靶点相互作用;(3)开发能够同时进行光交联和荧光开启的优秀光交联剂。考虑到这些因素,这些年来我们开发了三种版本的含“极简主义”生物正交手柄的光交联剂(L3-L6),并成功将它们应用于各种小生物活性分子的蛋白质标记和细胞成像研究。在本综述中,将特别突出并总结这些连接子的特点和功能。