去唾液酸糖蛋白受体
化学
甘露糖
树枝状大分子
内吞作用
PEG比率
甘露糖受体
聚乙二醇
转染
生物物理学
凝集素
基因传递
DNA
组合化学
受体
生物化学
体外
财务
经济
肝细胞
巨噬细胞
生物
基因
作者
Ricarda C. Steffens,Paul Folda,Nikole L. Fendler,Miriam Höhn,Katharina Bücher-Schossau,Susanne Kempter,Nicole L. Snyder,Laura Hartmann,Ernst Wagner,Simone Berger
标识
DOI:10.1021/acs.bioconjchem.3c00546
摘要
A cationic, dendrimer-like oligo(aminoamide) carrier with four-arm topology based on succinoyl tetraethylene pentamine and histidines, cysteines, and N-terminal azido-lysines was screened for plasmid DNA delivery on various cell lines. The incorporated azides allow modification with various shielding agents of different polyethylene glycol (PEG) lengths and/or different ligands by copper-free click reaction, either before or after polyplex formation. Prefunctionalization was found to be advantageous over postfunctionalization in terms of nanoparticle formation, stability, and efficacy. A length of 24 ethylene oxide repetition units and prefunctionalization of ≥50% of azides per carrier promoted optimal polyplex shielding. PEG shielding resulted in drastically reduced DNA transfer, which could be successfully restored by active lectin targeting via novel GalNAc or mannose ligands, enabling enhanced receptor-mediated endocytosis of the carrier system. The involvement of the asialoglycoprotein receptor (ASGPR) in the uptake of GalNAc-functionalized polyplexes was confirmed in the ASGPR-positive hepatocarcinoma cell lines HepG2 and Huh7. Mannose-modified polyplexes showed superior cellular uptake and transfection efficacy compared to unmodified and shielded polyplexes in mannose-receptor-expressing dendritic cell-like DC2.4 cells.
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