Group Competition Strategy for Covalent Ligand Discovery
As a powerful chemoproteomic tool, activity-based protein profiling (ABPP) has been extensively used for covalent ligand discovery. However, the current ABPP-based approaches are inherently based on indirect probe labeling competed by covalent ligands, and cannot directly compare the preferences of different ligands head-to-head. Herein, we report a group competition-based ABPP strategy (GC-ABPP) to allow the direct comparison of multiple ligands' binding ability on a proteome-wide scale. By dividing a library of fully functionalized probes (FFPs) into different subgroups and labeling the proteome simultaneously, the direct competition enables comparison of the labeling ability of different probes in drawing a global protein-ligand affinity metric. When it is applied to an expanded probe library, this strategy can be used iteratively to select the highest-affinity ligand toward a certain target protein in a multiple-round process. As a proof of concept, we synthesized 65 FFPs and employed the GC-ABPP to screen the ligand-protein reactivity for >6000 cysteine sites. After three rounds of screening, we identified high-affinity ligands targeting BCAT2 and UGDH. Our "multiple ligands versus multiple proteins" screening paradigm demonstrates great potential for applications in covalent ligand/drug discovery.
Authors
- Boyuan Zhao (ORCID: https://orcid.org/0000-0002-0827-7552)
- Chu Wang (ORCID: https://orcid.org/0000-0002-6925-1268)
- Zhihao Guo (ORCID: https://orcid.org/0009-0009-5349-2081)
- Weidi Xiao
- Yunzhu Meng
Institutions
- Ministry of Education of the People's Republic of China (CN)
- Peking University (CN)
- Beijing Normal University (CN)
- BC Platforms (Finland) (FI)
- Beijing National Laboratory for Molecular Sciences (CN)
- Center for Life Sciences (CN)
Publication Details
- Journal
- Journal of the American Chemical Society
- Published
- 2026-01-22
- DOI
- https://doi.org/10.1021/jacs.5c18150
- Primary Topic
- Click Chemistry and Applications
- Type
- article
- Field-Weighted Citation Impact
- 0.00