| Literature DB >> 30855951 |
Lik Hang Yuen1, Srikanta Dana1, Yu Liu2, Samuel I Bloom2, Ann-Gerd Thorsell3, Dario Neri4, Anthony J Donato2, Dmitri Kireev5, Herwig Schüler3, Raphael M Franzini1.
Abstract
DNA-encoded chemical libraries are increasingly used in pharmaceutical research because they enable the rapid discovery of synthetic protein ligands. Here we explored whether target-class focused DNA-encoded chemical libraries can be cost-effective tools to achieve robust screening productivity for a series of proteins. The study revealed that a DNA-encoded library designed for NAD+-binding pockets (NADEL) effectively sampled the chemical binder space of enzymes with ADP-ribosyltransferase activity. The extracted information directed the synthesis of inhibitors for several enzymes including PARP15 and SIRT6. The high dissimilarity of NADEL screening fingerprints for different proteins translated into inhibitors that showed selectivity for their target. The discovery of patterns of enriched structures for six out of eight tested proteins is remarkable for a library of 58 302 DNA-tagged structures and illustrates the prospect of focused DNA-encoded libraries as economic alternatives to large library platforms.Entities:
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Year: 2019 PMID: 30855951 DOI: 10.1021/jacs.8b08039
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419