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用于化学蛋白质组学的四嗪连接反应

Tetrazine ligation for chemical proteomics.

作者信息

Kang Kyungtae, Park Jongmin, Kim Eunha

机构信息

Department of Applied Chemistry, Kyung Hee University, Yongin, Gyeonggi 17104 Republic of Korea.

Center for Systems Biology, Massachusetts General Hospital, Harvard Medical School, 185 Cambridge St, CPZN 5206, Boston, Massachusetts 02114 USA.

出版信息

Proteome Sci. 2017 Jun 26;15:15. doi: 10.1186/s12953-017-0121-5. eCollection 2016.

Abstract

Determining small molecule-target protein interaction is essential for the chemical proteomics. One of the most important keys to explore biological system in chemical proteomics field is finding first-class molecular tools. Chemical probes can provide great spatiotemporal control to elucidate biological functions of proteins as well as for interrogating biological pathways. The invention of bioorthogonal chemistry has revolutionized the field of chemical biology by providing superior chemical tools and has been widely used for investigating the dynamics and function of biomolecules in live condition. Among 20 different bioorthogonal reactions, tetrazine ligation has been spotlighted as the most advanced bioorthogonal chemistry because of their extremely faster kinetics and higher specificity than others. Therefore, tetrazine ligation has a tremendous potential to enhance the proteomic research. This review highlights the current status of tetrazine ligation reaction as a molecular tool for the chemical proteomics.

摘要

确定小分子与目标蛋白的相互作用对于化学蛋白质组学至关重要。探索化学蛋白质组学领域生物系统的最重要关键之一是找到一流的分子工具。化学探针可以提供出色的时空控制,以阐明蛋白质的生物学功能以及探究生物途径。生物正交化学的发明通过提供卓越的化学工具彻底改变了化学生物学领域,并已广泛用于研究活细胞条件下生物分子的动力学和功能。在20种不同的生物正交反应中,四嗪连接因其极其快速的动力学和比其他反应更高的特异性而成为最先进的生物正交化学,备受关注。因此,四嗪连接在增强蛋白质组学研究方面具有巨大潜力。本综述重点介绍了四嗪连接反应作为化学蛋白质组学分子工具的现状。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2291/5485739/a1c163c95ca1/12953_2017_121_Fig1_HTML.jpg

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