Magainin 2-derived stapled peptides derived with the ability to deliver pDNA, mRNA, and siRNA into cells

被引:6
作者
Hirano, Motoharu [1 ,2 ]
Yokoo, Hidetomo [1 ,3 ]
Goto, Chihiro [1 ,2 ]
Oba, Makoto [3 ]
Misawa, Takashi [1 ]
Demizu, Yosuke [1 ,2 ,4 ]
机构
[1] Natl Inst Hlth Sci, Div Organ Chem, 3-25-26 Tonomachi, Kawasaki, Kanagawa 2109501, Japan
[2] Yokohama City Univ, Grad Sch Med Life Sci, I-7-29 Yokohama, Yokohama, Kanagawa 2300045, Japan
[3] Kyoto Prefectural Univ Med, Grad Sch Med Sci, Med Chem, Kyoto 6060823, Japan
[4] Okayama Univ, Div Pharmaceut Sci, Grad Sch Med Dent & Pharmaceut Sci, I-1-1 Tsushimanaka, Kita 7008530, Japan
关键词
ARGININE-RICH PEPTIDES; PENETRATING PEPTIDES; ANTIMICROBIAL PEPTIDES; CELLULAR UPTAKE; TAT PROTEIN; TRANSLOCATION; MEMBRANE; HELIX;
D O I
10.1039/d3sc04124g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We have developed cell-penetrating stapled peptides based on the amphipathic antimicrobial peptide magainin 2 for intracellular delivery of nucleic acids such as pDNA, mRNA, and siRNA. Various types of stapled peptides with a cross-linked structure were synthesised in the hydrophobic region of the amphipathic structure, and their efficacy in intracellular delivery of pDNA was evaluated. The results showed that the stapled peptide st7-5 could deliver pDNA into cells. To improve the deliverability of st7-5, we further designed st7-5_R, in which the Lys residues were replaced by Arg residues. The peptide st7-5_R formed compact and stable complexes with pDNA and was able to efficiently transfer pDNA into the cell. In addition to pDNA, st7-5_R was also able to deliver mRNA and siRNA into the cell. Thus, st7-5_R is a novel peptide that can achieve efficient intracellular delivery of three different nucleic acids. We have developed cell-penetrating stapled peptides based on the amphipathic antimicrobial peptide magainin 2 for intracellular delivery of nucleic acids such as pDNA, mRNA, and siRNA.
引用
收藏
页码:10403 / 10410
页数:9
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