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通过氨基上的生物可逆精氨酸修饰(BioRAM)实现天然蛋白质的细胞内递送

Intracellular Delivery of Native Proteins by BioReversible Arginine Modification (BioRAM) on Amino Groups.

作者信息

Franke Jonathan, Arafiles Jan Vincent V, Leis Christian, Hackenberger Christian P R

机构信息

Department of Chemical Biology, Leibniz-Forschungsinstitut für Molekulare Pharmakologie (FMP), Robert-Rössle-Strasse 10, 13125, Berlin, Germany.

Department of Chemistry, Humboldt Universität zu Berlin, Brook-Taylor-Straße 2, 12489, Berlin, Germany.

出版信息

Angew Chem Int Ed Engl. 2025 Aug 18;64(34):e202506802. doi: 10.1002/anie.202506802. Epub 2025 Jul 9.

Abstract

Protein-based tools are emerging as innovative solutions to interfere with biological pathways in molecular biology and medicine. They offer advantages over traditional small molecules due to their adaptable structural diversity and their ability to engage previously inaccessible cellular targets. However, most proteins do not penetrate the lipid bilayer of mammalian cells and are therefore restricted to extracellular targets. Despite recent advances, a general method for the delivery of functional proteins into human cells remains a significant challenge. In this study, we present a bioreversible protein modification strategy of amines using short arginine-containing peptides (termed BioRAM) that enables cytosolic delivery starting from genetically non-engineered proteins. We optimized the bioconjugation strategy to achieve fast intracellular cleavage and complete recovery of the native protein. In combination with our previously established cell-penetrating peptide (CPP)-additive protocol, we show superior delivery of fluorescent protein and functional RNase A into the cytosol, achieving physiological response. Moreover, we are able to demonstrate the excellent performance of BioRAM in the presence of serum, thereby broadening the scope for intracellular applications of functional proteins.

摘要

基于蛋白质的工具正成为分子生物学和医学中干扰生物途径的创新解决方案。由于其适应性的结构多样性以及与以前难以接近的细胞靶点结合的能力,它们相对于传统小分子具有优势。然而,大多数蛋白质无法穿透哺乳动物细胞的脂质双层,因此仅限于细胞外靶点。尽管最近取得了进展,但将功能性蛋白质递送至人类细胞的通用方法仍然是一项重大挑战。在本研究中,我们提出了一种使用含精氨酸的短肽对胺进行生物可逆蛋白质修饰的策略(称为BioRAM),该策略能够从非基因工程改造的蛋白质开始实现胞质递送。我们优化了生物共轭策略,以实现快速的细胞内切割和天然蛋白质的完全恢复。结合我们之前建立的细胞穿透肽(CPP)添加方案,我们展示了荧光蛋白和功能性核糖核酸酶A向胞质溶胶的卓越递送,实现了生理反应。此外,我们能够证明BioRAM在血清存在下的优异性能,从而拓宽了功能性蛋白质细胞内应用的范围。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13a9/12363615/9ac5452cb9c2/ANIE-64-e202506802-g007.jpg

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