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Identification and validation of WDR5 WIN-site ligands via DNA-encoded chemical library screening.

Authors :
Ding B
Lu L
Hu J
Zhang R
Wang F
Zhou Z
Lin Y
Pan C
Zhou Y
Yang B
Zhu CL
Zhou C
Cao J
Source :
Bioorganic chemistry [Bioorg Chem] 2024 Nov 22; Vol. 154, pp. 107948. Date of Electronic Publication: 2024 Nov 22.
Publication Year :
2024
Publisher :
Ahead of Print

Abstract

WD repeat-containing protein 5 (WDR5) is a scaffolding protein involved in critical protein-protein interactions and a promising target for therapeutic development. Novel small-molecule ligands targeting WDR5 were identified using the DELopen platform, a free-access DNA-encoded chemical library (DEL) for academic research. Through off-DNA structure-activity relationship studies and photoaffinity labeling, two promising initial leads, DBL-6-13 and DBL-6-33, were identified as new binders of WDR5. These compounds exhibited moderate to good binding affinities and were confirmed to bind the WIN-site through co-crystal structure analysis. Our findings demonstrate the utility of DEL technology in identifying ligands for challenging targets like WDR5, particularly within an academic research setting using the DELopen platform. The identified WDR5 ligands offer a foundation for further optimization and exploration as chemical probes for WDR5 research.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper. In fact, none of the authors in this work is an Editorial Board Member/Editor-in-Chief/Associate Editor/Guest Editor for Bioorganic Chemistry.<br /> (Copyright © 2024 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1090-2120
Volume :
154
Database :
MEDLINE
Journal :
Bioorganic chemistry
Publication Type :
Academic Journal
Accession number :
39616835
Full Text :
https://doi.org/10.1016/j.bioorg.2024.107948