Intracellular delivery of nanopartides via the HIV-1 tat pepticle

被引:82
作者
Berry, C. C. [1 ]
机构
[1] Univ Glasgow, Ctr Cell Engn, Glasgow G12 8QQ, Lanark, Scotland
关键词
cell uptake; gold nanoparticles; liposomes; magnetic nanoparticles; nanoparticles; nuclear targeting; quantum dots; tat;
D O I
10.2217/17435889.3.3.357
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Functionalized nanoparticles are heralded as part of the future with regards to targeted cell and nuclear delivery. However, direct intracellular and intranuclear delivery has, until recently, been difficult to achieve owing to the impermeable nature of the plasma and nuclear membranes. During the past 15 years, a range of peptides, termed cell-penetrating peptides (CPPs), which have the ability to translocate into living cells, have been discovered. Thus, in more recent years, the combination of CPPs with nanoparticles, enabling CPP-mediated cell delivery, has opened up many avenues of research. This review discusses the use of various CPPs, focusing on tat peptide, to functionalize nanoparticles and the possible move from the laboratory to the clinic.
引用
收藏
页码:357 / 365
页数:9
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