On-DNA hit validation methodologies for ligands identified from DNA-encoded chemical libraries

被引:19
|
作者
Prati, Luca [1 ]
Bigatti, Martina [1 ]
Donckele, Etienne J. [1 ]
Neri, Dario [2 ]
Samain, Florent [1 ]
机构
[1] Philochem AG, Libernstr 3, CH-8112 Otelfingen, Switzerland
[2] Swiss Fed Inst Technol, Dept Chem & Appl Biosci, Vladimir Prelog Weg 3, CH-8093 Zurich, Switzerland
基金
欧洲研究理事会; 瑞士国家科学基金会;
关键词
DNA-Encoded chemical library; Hit validation methodology; ELISA; SPR; CARBONIC-ANHYDRASE IX; INHIBITORS; AFFINITY; ENABLES; IMPACT;
D O I
10.1016/j.bbrc.2020.04.030
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
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. (C) 2020 Published by Elsevier Inc.
引用
收藏
页码:235 / 240
页数:6
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