Soomets U, Hällbrink M, Langel U
Department of Neurochemistry and Neurotoxicology, Arrhenius Laboratories, Stockholm University, S-10691 Stockholm, Sweden.
Front Biosci. 1999 Nov 1;4:D782-6. doi: 10.2741/soomets.
PNA is a nucleic acid analog with an achiral polyamide backbone consisting of N-(2-aminoethyl)glycine units (figure 1). The purine or pyrimidine bases are linked to the each unit via a methylene carbonyl linker (1-3) to target the complementary nucleic acid (4). PNA binds to complementary RNA or DNA in a parallel or antiparallel orientation following the Watson-Crick base-pairing rules (5-7). The uncharged nature of the PNA oligomers enhances the stability of the hybrid PNA/DNA(RNA) duplexes as compared to the natural homoduplexes. The non-natural character of the PNA makes PNA oligomers highly resistant to protease and nuclease attacks (8). These properties of PNA oligomers suggest that they could potentially serve as efficient antisense or antigene reagents. Indeed, peptide nucleic acids have been applied to block protein expression on the transcriptional (9) and translational level (10,11), and microinjected PNA oligomers demonstrate a strong antisense effect in intact cells (12). However, contrary to the "normal" nucleic acid analogs, PNA oligomers are not efficiently delivered into the cytoplasm of the cell, and until recently this has hindered the application of PNA oligomers as antisense reagents. In this work we summarize some recent achievements on PNA antisense application, especially these concerned with whole cell or tissue delivery of the PNA.
肽核酸(PNA)是一种核酸类似物,其具有由N-(2-氨基乙基)甘氨酸单元组成的非手性聚酰胺主链(图1)。嘌呤或嘧啶碱基通过亚甲基羰基连接子与每个单元相连(1-3),以靶向互补核酸(4)。PNA按照沃森-克里克碱基配对规则,以平行或反平行方向与互补RNA或DNA结合(5-7)。与天然同源双链体相比,PNA寡聚物的不带电性质增强了杂交PNA/DNA(RNA)双链体的稳定性。PNA的非天然特性使PNA寡聚物对蛋白酶和核酸酶的攻击具有高度抗性(8)。PNA寡聚物的这些特性表明它们有可能作为有效的反义或抗基因试剂。事实上,肽核酸已被应用于在转录水平(9)和翻译水平(10,11)阻断蛋白质表达,并且显微注射的PNA寡聚物在完整细胞中表现出强烈的反义效应(12)。然而,与“正常”核酸类似物相反,PNA寡聚物不能有效地递送到细胞的细胞质中,直到最近这一直阻碍着PNA寡聚物作为反义试剂的应用。在这项工作中,我们总结了PNA反义应用方面的一些最新成果,特别是那些与PNA的全细胞或组织递送有关的成果。