Cell-permeable peptides improve cellular uptake and therapeutic gene delivery of replication-deficient viruses in cells and in vivo

被引:158
作者
Gratton, JP
Yu, J
Griffith, JW
Babbitt, RW
Scotland, RS
Hickey, R
Giordano, FJ
Sessa, WC [1 ]
机构
[1] Yale Univ, Sch Med, Dept Pharmacol, Boyer Ctr Mol Med, New Haven, CT 06510 USA
[2] Yale Univ, Sch Med, Dept Cardiovasc Med,Boyer Ctr Mol Med, Vasc Cell Signaling & Therapeut Program, New Haven, CT 06510 USA
关键词
D O I
10.1038/nm835
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Small polybasic peptides derived from the transduction domains of certain proteins, such as the third alpha-helix of the Antennapedia (Antp) homeodomain, can cross the cell membrane through a receptor-independent mechanism. These cell-permeable molecules have been used as 'Trojan horses' to introduce biologically active cargo molecules such as DNA, peptides or proteins into cells. Using these cell-permeable peptides, we have developed an efficient and simple method to increase virally mediated gene delivery and protein expression in vitro and in vivo. Here, we show that cell-permeable peptides increase viral cell entry, improve gene expression at reduced titers of virus and improve efficacy of therapeutically relevant genes in vivo.
引用
收藏
页码:357 / 362
页数:6
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