糖基转移酶
高通量筛选
变构调节
化学
生物化学
转移酶
药物发现
酶
计算生物学
生物
作者
Xinjian Yin,Jiaxin Li,Senhua Chen,Yuping Wu,Zhigang She,Lan Liu,Yue Wang,Zhizeng Gao
出处
期刊:ChemBioChem
[Wiley]
日期:2020-12-01
卷期号:22 (8): 1391-1395
被引量:7
标识
DOI:10.1002/cbic.202000746
摘要
O-GlcNAc transferase (OGT) is involved in many cellular processes, and selective OGT inhibitors are valuable tools to investigate O-GlcNAcylation functions, and could potentially lead to therapeutics. However, high-throughput OGT assays that are suitable for large-scale HTS and can identify inhibitors targeting both acceptor, donor sites, and allosteric binding-sites are still lacking. Here, we report the development of a high-throughput "FP-Tag" OGT assay with bovine serum albumin (BSA) as a low-cost and superior "FP-Tag". With this assay, 2-methyleurotinone was identified as a low-micromolar OGT inhibitor. This type of assay with BSA as "FP-Tag" would find more applications with other glycosyltransferases.
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