Issue 8, 2025

Functionally active modulators targeting the LRRK2 WD40 repeat domain identified by FRASE-bot in CACHE Challenge #1

Abstract

Critical Assessment of Computational Hit-Finding Experiments (CACHE) Challenges emerged as real-life stress tests for computational hit-finding strategies. In CACHE Challenge #1, 23 participants contributed their original workflows to identify small-molecule ligands for the WD40 repeat (WDR) of LRRK2, a promising Parkinson's target. We applied the FRASE-based hit-finding robot (FRASE-bot), a platform for interaction-based screening allowing a drastic reduction of the explorable chemical space and a concurrent detection of putative ligand-binding sites. In two screening rounds, 84 compounds were procured for experimental testing and 8 were confirmed to bind LRRK2-WDR with dissociation constants (Kd) ranging from 3 to 41 μM. To investigate the functional effect of WDR ligands, they were tested for their ability to modify the LRRK2 activity markers in HEK293T cells. Two compounds showed statistically significant increases in the kinase activity of WT LRRK2, and two compounds affected the conformation and kinase activity of major LRRK2 mutants.

Graphical abstract: Functionally active modulators targeting the LRRK2 WD40 repeat domain identified by FRASE-bot in CACHE Challenge #1

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Article information

Article type
Edge Article
Submitted
07 Лис 2024
Accepted
03 Січ 2025
First published
09 Січ 2025
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY-NC license

Chem. Sci., 2025,16, 3430-3439

Functionally active modulators targeting the LRRK2 WD40 repeat domain identified by FRASE-bot in CACHE Challenge #1

A. Mettu, M. Glavatskikh, X. Wang, A. J. Lara Ordóñez, F. Li, I. Chau, S. Ackloo, C. Arrowsmith, A. Bolotokova, P. Ghiabi, E. Gibson, L. Halabelian, S. Houliston, R. J. Harding, A. Hutchinson, P. Loppnau, S. Perveen, A. Seitova, H. Zeng, M. Schapira, J. Taymans and D. Kireev, Chem. Sci., 2025, 16, 3430 DOI: 10.1039/D4SC07532C

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