An overview of activity-based probes for glycosidases

被引:83
|
作者
Wu, Liang [1 ]
Armstrong, Zachary [1 ]
Schroeder, Sybrin P. [2 ]
de Boer, Casper [2 ]
Artola, Marta [2 ]
Aerts, Johannes M. F. G. [2 ]
Overkleeft, Herman S. [2 ]
Davies, Gideon J. [1 ]
机构
[1] Univ York, Dept Chem, York Struct Biol Lab, York YO10 5DD, N Yorkshire, England
[2] Leiden Univ, Leiden Inst Chem, Einsteinweg 55, NL-2300 RA Leiden, Netherlands
基金
欧洲研究理事会; 英国生物技术与生命科学研究理事会;
关键词
MECHANISM-BASED INACTIVATION; PROTEIN-PROFILING PROBES; IN-SITU VISUALIZATION; COVALENT INHIBITORS; FUNCTIONAL INTERROGATION; L-FUCOSIDASES; ENZYME; CYCLOPHELLITOL; IDENTIFICATION; GLUCOSIDASE;
D O I
10.1016/j.cbpa.2019.05.030
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
As the scope of modern genomics technologies increases, so does the need for informative chemical tools to study functional biology. Activity-based probes (ABPs) provide a powerful suite of reagents to probe the biochemistry of living organisms. These probes, featuring a specificity motif, a reactive chemical group and a reporter tag, are opening-up large swathes of protein chemistry to investigation in vitro, as well as in cellular extracts, cells and living organisms in vivo. Glycoside hydrolases, by virtue of their prominent biological and applied roles, provide a broad canvas on which ABPs may illustrate their functions. Here we provide an overview of glycosidase ABP mechanisms, and review recent ABP work in the glycoside hydrolase field, encompassing their use in medical diagnosis, their application for generating chemical genetic disease models, their fine-tuning through conformational and reactivity insight, their use for high-throughput inhibitor discovery, and their deployment for enzyme discovery and dynamic characterization.
引用
收藏
页码:25 / 36
页数:12
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