肽
生物化学
化学
细胞穿透肽
细胞毒性
娴熟的
荧光团
乙酰化
赖氨酸
结合
酶
体外
氨基酸
荧光
数学分析
物理
基因
量子力学
数学
作者
Sarah Hofmann,Carolin Sophie Dombrowsky,Dominic Happel,Cedric Dessin,Egzon Cermjani,Matijas Cica,Olga Avrutina,Norbert Sewald,Heinz Neumann,Harald Kolmar
标识
DOI:10.1021/acschembio.4c00149
摘要
The intracellular delivery of cargos via cell penetrating peptides (CPPs) holds significant promise as a drug delivery vehicle, but a major issue is their lack of cell type specificity, which can lead to detrimental off-target effects. We use an ADEPT-like concept to introduce conditional and selective activation of cellular uptake by using the lysine-rich, cationic, and amphiphilic L17E peptide as a model CPP. By masking the lysine residues of the L17E peptide with enzyme-cleavable acetyl protecting groups, the delivery of the covalently conjugated fluorophore TAMRA to HeLa cells was diminished. Recovery of cellular uptake could be achieved by deacetylation of the masked acetylated L17E peptide using the NAD-dependent sirtuin 2 (SirT2) deacetylase
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