Schulich Faculty of Chemistry, Technion-Israel Institute of Technology, 3200008, Haifa, Israel.
Angew Chem Int Ed Engl. 2021 Mar 22;60(13):7333-7343. doi: 10.1002/anie.202016208. Epub 2021 Feb 22.
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.
活细胞中递呈对特定靶标具有选择性的全合成蛋白是一种很有前途的方法,具有应用于基础研究和治疗的潜力。细胞穿透肽(CPPs)可实现蛋白的细胞递呈,但大多导致内体捕获,从而导致生物利用度降低。本文报道了一种 CPP 的设计和合成,该 CPP 融合了 4-((4-(二甲基氨基)苯基)偶氮)苯甲酸(DABCYL),以增强低微摩尔浓度下荧光标记的合成蛋白类似物的细胞摄取。将带有单个赖氨酸的环状 deca-精氨酸(cR10)与 DABCYL 连接,用于合成泛素(Ub)和小泛素样修饰物-2(SUMO-2)支架,与未修饰的 cR10 相比,活细胞中的摄取效率提高了三倍。我们还可以实现 cR10DABCYL 辅助递呈 Ub 和 Ub 变体(Ubv),作为基于活性的探针,用于在活细胞中研究去泛素化酶的功能。