Cell Penetrating Peptides and the Mechanisms for Intracellular Entry

被引:40
作者
Choi, Young S. [1 ]
David, Allan E. [1 ]
机构
[1] Auburn Univ, Dept Chem Engn, Auburn, AL 36849 USA
基金
美国国家科学基金会;
关键词
Cell penetrating peptide; cellular uptake; drug delivery; lipid bilayer; endocytosis; ARGININE-RICH PEPTIDES; TAT-FUSION PROTEINS; PLASMA-MEMBRANE; ANTENNAPEDIA HOMEODOMAIN; LIPID-BILAYERS; 3RD HELIX; DELIVERY; TRANSDUCTION; CARRIER; MODEL;
D O I
10.2174/1389201015666140617093331
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
A major thrust in the biomedical and pharmaceutical industries is to develop diagnostic and therapeutic tools that have significantly improved selectivity and specificity compared to the current state-of-the-art. This has driven much of the effort to look at molecules and materials that are significantly larger than the traditional small molecule agents. Due to size restrictions, however, many of these materials are unable to penetrate the cell membrane and gain access to the intracellular components on which they exert their action. The relatively recent discovery of cell penetrating peptides (CPP) provides a powerful tool that has enabled the intracellular delivery of these materials. While a variety of proteins, DNA, polymers and even nanoparticles have been successfully delivered into cells, there still remains some debate as to the mechanism of entry utilized by the CPPs. In this review, we provide a brief outline of the different potential mechanisms for cellular uptake of CPPs.
引用
收藏
页码:192 / 199
页数:8
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