A resource to enable chemical biology and drug discovery of WDR Proteins

Cheryl H Arrowsmith, Suzanne Ackloo, Fengling Li, Magda Szewczyk, Almagul Seitova, Peter Loppnau, Hong Zeng, Shabbir Ahmad, Serap Beldar, Albina Bolotokova, Irene Chau, Saba Dehghani-Tafti, Aiping Dong, Pegah Ghiabi, Elisa Gibson, Stuart R Green, Oleksandra Herasymenko,Scott Houliston, Ashley Hutchinson, Serah W Kimani, Maria Kutera, Haejin A Kwak, Yanjun Li, Raquel AC Machado, Sumera Perveen, Germanna L Righetto, Suman Shrestha, Madhushika Silva, Manisha Yadav, Aliakbar K Yazdi, Vijayaratnam Santhakumar, Aled M Edwards, Dalia Barsyte-Lovejoy, Matthieu Schapira, Peter J Brown, Levon Halabelian,Jin Xu, Jianwen A Feng,Steven Kearnes, James Thompson,Wen Torng,Justin Gilmer, Patrick Riley, Ian Watson, Yelena A Arnautova, AJ Baghaie,John W Cuozzo,Jeremy S Disch, Antoine Dumas, Nathan Harms, Jenny Liu,Eric A Sigel, Brian Goldman, Trevor Kramer, Christopher A Mulhern,Belinda L Slakman, Carl Underkoffler,Moritz von Rechenberg, Paolo A Centrella,Matthew A Clark,Marie-Aude Guie, John P Gullinger,Anthony D Keefe, Rhys D Taylor,Junyi Zhang,Ying Zhang, Cristina Lento,Derek J Wilson, Esther Wolf, Joachim Loup, Michael D Sintchak

biorxiv(2024)

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摘要
Protein class-focused drug discovery has a long and successful history in pharmaceutical research, yet most members of druggable protein families remain unliganded, often for practical reasons. Here we combined experiment and computation to enable discovery of ligands for WD40 repeat (WDR) proteins, one of the largest human protein families. This resource includes expression clones, purification protocols, and a comprehensive assessment of the druggability for hundreds of WDR proteins. We solved 21 high resolution crystal structures, and have made available a suite of biophysical, biochemical, and cellular assays to facilitate the discovery and characterization of small molecule ligands. To this end, we use the resource in a hit-finding pilot involving DNA-encoded library (DEL) selection followed by machine learning (ML). This led to the discovery of first-in-class, drug-like ligands for 9 of 20 targets. This result demonstrates the broad ligandability of WDRs. This extensive resource of reagents and knowledge will enable further discovery of chemical tools and potential therapeutics for this important class of proteins. ### Competing Interest Statement BLS, BG, JSD, JZ, JWC, MvR, PR, SK, and TK are employees and shareholders of Relay Therapeutics.
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