Armitage Bruce A
Dept of Chemistry, Carnegie Mellon University, 4400 Fifth Avenue, Pittsburgh, PA 15213-3890, USA.
Drug Discov Today. 2003 Mar 1;8(5):222-8. doi: 10.1016/s1359-6446(03)02611-4.
Hybridization of oligonucleotides and their analogues to complementary DNA or RNA sequences is complicated by the presence of secondary and tertiary structure in the target. In particular, folding of the target nucleic acid imposes substantial thermodynamic penalties to hybridization. Slower kinetics for hybridization can also be observed, relative to an unstructured target. The development of high affinity oligonucleotide analogues such as peptide nucleic acid (PNA) can compensate for the thermodynamic and kinetic barriers to hybridization. Examples of structured targets successfully hybridized by PNA oligomers include DNA duplexes, DNA hairpins, DNA quadruplexes and an RNA hairpin embedded within a mRNA.
寡核苷酸及其类似物与互补DNA或RNA序列的杂交会因靶标中二级和三级结构的存在而变得复杂。特别是,靶标核酸的折叠对杂交造成了相当大的热力学阻碍。相对于无结构的靶标,还可观察到杂交动力学较慢。高亲和力寡核苷酸类似物如肽核酸(PNA)的开发可以弥补杂交的热力学和动力学障碍。成功与PNA寡聚物杂交的结构化靶标的例子包括DNA双链体、DNA发夹、DNA四链体以及嵌入mRNA中的RNA发夹。