Philochem AG, Libernstrasse 3, CH-8112, Otelfingen, Switzerland.
Department of Chemistry and Applied Biosciences, Swiss Federal Institute of Technology (ETH Zürich), Vladimir-Prelog-Weg 3, CH-8093, Zürich, Switzerland.
Biochem Biophys Res Commun. 2020 Dec 3;533(2):235-240. doi: 10.1016/j.bbrc.2020.04.030. Epub 2020 Apr 30.
DNA-encoded chemical libraries (DECLs) are large compound collections attached to DNA fragments, serving as amplifiable barcodes, which can be screened on target proteins of pharmaceutical interest. In DECL selections, ligands are identified by high-throughput DNA sequencing, by comparing their frequency before and after the affinity capture step. Hits identified using this procedure need to be validated by resynthesis and by performing affinity measurements. Here we report novel on-DNA hit validation strategies, which enable the facile confirmation of ligand-protein interaction as well as the determination of equilibrium and kinetic binding constants. The experimental procedures, which had been inspired by enzyme-linked immunosorbent assays (ELISA), were validated using ligands of different affinity to carbonic anhydrase II and IX.
DNA 编码的化学文库 (DECLs) 是附着在 DNA 片段上的大型化合物集合,作为可扩增的条形码,可以在药物靶点的蛋白质上进行筛选。在 DECL 选择中,通过高通量 DNA 测序来识别配体,通过比较亲和捕获步骤前后的频率。使用此程序识别的命中需要通过重新合成和进行亲和测量来验证。在这里,我们报告了新的 DNA 命中验证策略,这些策略能够轻松确认配体-蛋白质相互作用,并确定平衡和动力学结合常数。这些实验程序受到酶联免疫吸附测定 (ELISA) 的启发,使用不同亲和力的碳酸酐酶 II 和 IX 的配体进行了验证。