Intracellular Delivery of Plasmid DNA Using Amphipathic Helical Cell-Penetrating Peptides Containing Dipropylglycine

被引:0
|
作者
Naka, Motoki [1 ]
Umeno, Tomohiro [1 ]
Shibuya, Mika [2 ]
Yamaberi, Yuto [2 ]
Ueda, Atsushi [2 ]
Tanaka, Masakazu [2 ]
Takemoto, Hiroyasu [1 ]
Oba, Makoto [1 ]
机构
[1] Kyoto Prefectural Univ Med, Grad Sch Med Sci, Sakyo Ku, 1-5 Shimogamohangi Cho, Kyoto 6060823, Japan
[2] Nagasaki Univ, Grad Sch Biomed Sci, 1-14 Bunkyo Machi, Nagasaki 8528521, Japan
基金
日本科学技术振兴机构;
关键词
cell-penetrating peptide; plasmid DNA (pDNA) delivery; helical structure; amphipathic structure; unnatural amino acid; ALPHA-AMINO-ACIDS; ABILITIES;
D O I
10.1248/cpb.c24-00221
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Cell-penetrating peptides (CPPs) serve as potent vehicles for delivering membrane -impermeable compounds, including nucleic acids, into cells. In a previous study, we reported the successful intracellular delivery of small interfering RNAs (siRNAs) with negligible cytotoxicity using a peptide containing an unnatural amino acid (dipropylglycine). In the present study, we employed the same seven peptides as the previous study to evaluate their efficacy in delivering plasmid DNA (pDNA) intracellularly. Although pDNA and siRNA are nucleic acids, they differ in size and biological function, which may influence the optimal peptide sequences for their delivery. Herein, three peptides demonstrated effective pDNA transfection abilities. Notably, only one of the three peptides previously exhibited efficient gene-silencing effect with siRNA. These findings validate our hypothesis and offer insights for the personalized design of CPPs for the delivery of pDNA and siRNA.
引用
收藏
页码:512 / 517
页数:6
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