| Literature DB >> 29856130 |
Nicholas Favalli1, Stefan Biendl1, Marco Hartmann1, Jacopo Piazzi2, Filippo Sladojevich3, Susanne Gräslund4,5, Peter J Brown4, Katja Näreoja5, Herwig Schüler5, Jörg Scheuermann1, Raphael Franzini1,6, Dario Neri1.
Abstract
A DNA-encoded chemical library (DECL) with 1.2 million compounds was synthesized by combinatorial reaction of seven central scaffolds with two sets of 343×492 building blocks. Library screening by affinity capture revealed that for some target proteins, the chemical nature of building blocks dominated the selection results, whereas for other proteins, the central scaffold also crucially contributed to ligand affinity. Molecules based on a 3,5-bis(aminomethyl)benzoic acid core structure were found to bind human serum albumin with a Kd value of 6 nm, while compounds with the same substituents on an equidistant but flexible l-lysine scaffold showed 140-fold lower affinity. A 18 nm tankyrase-1 binder featured l-lysine as linking moiety, while molecules based on d-Lysine or (2S,4S)-amino-l-proline showed no detectable binding to the target. This work suggests that central scaffolds which predispose the orientation of chemical building blocks toward the protein target may enhance the screening productivity of encoded libraries.Entities:
Keywords: DNA-encoded chemical libraries; bifunctional ligands; human serum albumin; tankyrase-1
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Year: 2018 PMID: 29856130 PMCID: PMC6126618 DOI: 10.1002/cmdc.201800193
Source DB: PubMed Journal: ChemMedChem ISSN: 1860-7179 Impact factor: 3.466