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[一种用于生物活性小分子靶点鉴定的新型亲和标记方法的开发]

[Development of a Novel Affinity Labeling Method for Target Identification of Bioactive Small Molecules].

作者信息

Yamaguchi Takao

机构信息

Graduate School of Pharmaceutical Sciences, Osaka University.

出版信息

Yakugaku Zasshi. 2019;139(12):1513-1521. doi: 10.1248/yakushi.19-00171.

DOI:10.1248/yakushi.19-00171
PMID:31787638
Abstract

Target identification (target-ID) is an important step in elucidating the mechanisms of action of bioactive small molecules. In the past few decades, a number of target-ID methods have been developed. Among these, affinity labeling has been reliably used for specific modifications, as well as for the identification of weakly interacting protein targets, membrane-associated protein targets, and target-interacting proteins under native cellular conditions, which are generally difficult to achieve by conventional pull-down methods. In general, affinity labeling utilizes chemical probes composed of a bioactive small molecule, a reactive group, and a detection unit. However, the design and synthesis of highly functionalized chemical probes is often time-consuming. To address this issue, we have recently developed some simple affinity labeling methods using small fluorogenic tags, such as 4-alkoxy-7-nitro-2,1,3-benzoxadiazole (O-NBD), 2,3-dichloromaleimide (diCMI), and 4-azidophthalimide (AzPI), and successfully achieved the specific fluorescent labeling of target proteins, even in living cells. These methods should be useful for target-ID in phenotypic drug discovery.

摘要

靶点鉴定(target-ID)是阐明生物活性小分子作用机制的重要步骤。在过去几十年里,已开发出多种靶点鉴定方法。其中,亲和标记已被可靠地用于特异性修饰,以及在天然细胞条件下鉴定弱相互作用蛋白靶点、膜相关蛋白靶点和靶点相互作用蛋白,而这些通常难以通过传统的下拉法实现。一般来说,亲和标记利用由生物活性小分子、反应基团和检测单元组成的化学探针。然而,高功能化化学探针的设计和合成通常很耗时。为了解决这个问题,我们最近开发了一些使用小型荧光标签的简单亲和标记方法,如4-烷氧基-7-硝基-2,1,3-苯并恶二唑(O-NBD)、2,3-二氯马来酰亚胺(diCMI)和4-叠氮基邻苯二甲酰亚胺(AzPI),并成功实现了靶蛋白的特异性荧光标记,甚至在活细胞中也是如此。这些方法在表型药物发现中的靶点鉴定方面应该会很有用。

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