Abstract
Live-cell delivery of a fully synthetic protein having selectivity towards a particular target is a promising approach with potential applications for basic research and therapeutics. Cell-penetrating peptides (CPPs) allow the cellular delivery of proteins but mostly result in endosomal entrapment, leading to lack of bioavailability. Herein, we report the design and synthesis of a CPP fused to 4-((4-(dimethylamino)phenyl)azo)benzoic acid (DABCYL) to enhance cellular uptake of fluorescently labelled synthetic protein analogues in low micromolar concentration. The attachment of cyclic deca-arginine (cR10) modified with a single lysine linked to DABCYL to synthetic ubiquitin (Ub) and small ubiquitin-like modifier-2 (SUMO-2) scaffolds resulted in a threefold higher uptake efficacy in live cells compared to the unmodified cR10. We could also achieve cR10DABCYL-assisted delivery of Ub and a Ub variant (Ubv) based activity-based probes for functional studies of deubiquitinases in live cells.
Original language | American English |
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Pages (from-to) | 7333-7343 |
Number of pages | 11 |
Journal | Angewandte Chemie - International Edition |
Volume | 60 |
Issue number | 13 |
DOIs | |
State | Published - 22 Mar 2021 |
Keywords
- activity-based probes
- cell-penetrating peptides
- fluorescence
- small ubiquitin like modifier (SUMO)
- ubiquitin
All Science Journal Classification (ASJC) codes
- Catalysis
- General Chemistry