An Economical High-Throughput "FP-Tag" Assay for Screening Glycosyltransferase Inhibitors*.
Xinjian YinJiaxin LiSenhua ChenYuping WuZhigang SheLan LiuYue WangZhi-Zeng GaoPublished in: Chembiochem : a European journal of chemical biology (2021)
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.