Cell-Penetrating Peptides: Design, Synthesis, and Applications

被引:848
作者
Copolovici, Dana Maria [1 ]
Langel, Kent [1 ]
Eriste, Elo [1 ]
Langel, Ulo [1 ,2 ]
机构
[1] Univ Tartu, Mol Biotechnol Lab, Inst Technol, EE-50411 Tartu, Estonia
[2] Stockholm Univ, Dept Neurochem, Arrhenius Labs Nat Sci, SE-10691 Stockholm, Sweden
基金
瑞典研究理事会;
关键词
cell-penetrating peptides; delivery agents; uptake mechanism; nanoparticles; gene therapy; nucleic acids; ARGININE-RICH PEPTIDES; PROTEIN TRANSDUCTION DOMAINS; TAT-FUSION PROTEINS; D-ISOMER PEPTIDES; HEPARAN-SULFATE; PRION PROTEIN; INTERNALIZATION MECHANISMS; ANTENNAPEDIA HOMEODOMAIN; ANTIMICROBIAL PEPTIDES; MEMBRANE PERTURBATION;
D O I
10.1021/nn4057269
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
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.
引用
收藏
页码:1972 / 1994
页数:23
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