Conjugates of oligonucleotides and analogues with cell penetrating peptides as gene silencing agents

被引:75
|
作者
Zatsepin, TS
Turner, JJ
Oretskaya, TS
Gait, MJ
机构
[1] MRC, Mol Biol Lab, Cambridge CB2 2QH, England
[2] Moscow MV Lomonosov State Univ, Dept Chem, Moscow 119992, Russia
[3] Moscow MV Lomonosov State Univ, AN Belozersky Inst Physicochem Biol, Moscow 119992, Russia
基金
英国惠康基金;
关键词
oligonucleotide; conjugate; gene silencing; antisense; cell penetrating peptide;
D O I
10.2174/138161205774580769
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The review describes key aspects of the synthesis and biological activities of conjugates of oligonucleotides and their analogues with synthetic peptides, in particular aimed towards gene silencing applications. The common methods of synthesis of oligonucleotide-peptide conjugates (OPCs) and PNA-peptide conjugates (PPCs) are described, which include both total solid-phase and fragment coupling approaches. In addition, various applications of conjugates as gene silencing agents are outlined. These include antisense and steric block applications in mammalian cells of OPCs, PPCs and phosphorodiamidate morpholinooligonucleotide (PMO)-peptide conjugates, gene silencing in bacteria, various DNA targeting applications, and recent reports of gene silencing activities of siRNA-peptide conjugates. A table listing all peptides used as oligonucleotide conjugates for gene silencing applications is also included.
引用
收藏
页码:3639 / 3654
页数:16
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