细胞穿透肽
内吞作用
基因传递
核酸
细胞
肽
纳米技术
基因沉默
共轭体系
DNA
化学
计算生物学
遗传增强
细胞生物学
基因
生物化学
材料科学
生物
有机化学
聚合物
作者
Dana Maria Copolovici,Kent Langel,Elo Eriste,Ülo Langel
出处
期刊:ACS Nano
[American Chemical Society]
日期:2014-02-24
卷期号:8 (3): 1972-1994
被引量:803
摘要
The intrinsic property of cell-penetrating peptides (CPPs) to deliver therapeutic molecules (nucleic acids, drugs, imaging agents) to cells and tissues in a nontoxic manner has indicated that they may be potential components of future drugs and disease diagnostic agents. These versatile peptides are simple to synthesize, functionalize, and characterize yet are able to deliver covalently or noncovalently conjugated bioactive cargos (from small chemical drugs to large plasmid DNA) inside cells, primarily via endocytosis, in order to obtain high levels of gene expression, gene silencing, or tumor targeting. Typically, CPPs are often passive and nonselective yet must be functionalized or chemically modified to create effective delivery vectors that succeed in targeting specific cells or tissues. Furthermore, the design of clinically effective systemic delivery systems requires the same amount of attention to detail in both design of the delivered cargo and the cell-penetrating peptide used to deliver it.
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