Internal Ubiquitin Electrophiles for Covalent Trapping and Inhibition of Deubiquitinases

GA: Genetically encoded internal electrophiles in ubiquitin (Ub) enable the profiling of multivalent interaction interfaces, addressing a key limitation of current Ub-based activity-based probes. In this study, these probes capture a Ub–deubiquitinase interaction with minimal structural perturbation and serve as selective diUb probes that covalently target the catalytic cysteines of Met1-specific Dubs.

The ubiquitin (Ub) system governs vital cellular processes in eukaryotic biology through an intricate network of Ub–protein interactions. While semisynthetic C-terminal Ub electrophiles (UbEs) are widely used to study Ub transfer and deubiquitinase (Dub) activity, they are limited to probing the active site while leaving other functionally important sites unexplored. Building on previously identified multivalent interaction interfaces and potential allosteric sites which are key to understanding their dynamic nature, here we report the development of genetically encoded Ub-based probes to covalently tether Ub-protein interactions in a proximity-driven manner at distal locations away from the active site. This study demonstrates that UbEs with internal electrophiles maintain conformational changes observed with their C-terminal counterparts while circumventing their limitations in capturing distal binding-site complexes, an emerging feature in Ub-mediated regulation. Genetically encoding these electrophiles further demonstrate rational variation as activity-based probes (ABP), leading to a Met1-diUb ABP showing preference for OTULIN over other Met1 cleaving Dubs. Taken together, our study introduces genetically encoded Ub-based probes to explore the structural and biochemical significance of Ub-Dub interactions beyond the canonical S1 site, overcoming some limitations of traditional Ub C-terminal electrophiles.

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