Bukanov N O, Demidov V V, Nielsen P E, Frank-Kamenetskii M D
Center for Advanced Biotechnology, Department of Biomedical Engineering, Boston University, 36 Cummington Street, Boston, MA 02215, USA.
Proc Natl Acad Sci U S A. 1998 May 12;95(10):5516-20. doi: 10.1073/pnas.95.10.5516.
A stable complex between duplex DNA and an oligonucleotide is assembled with the aid of a DNA synthetic mimic, peptide nucleic acid (PNA). Homopyrimidine PNAs are known to invade into short homopurine tracts in duplex DNA forming P-loops. We have found that P-loops, formed at two closely located purine tracts in the same DNA strand separated by a mixed purine-pyrimidine sequence, merge and open the double helix between them. The opposite DNA strand, which is not bound with PNA, exposes and becomes accessible for complexing with an oligonucleotide via Watson-Crick pairing. As a result, the PD-loop emerges, which consists of locally open duplex DNA, PNA "openers," and an oligonucleotide. The PD-loop stability and sequence specificity are demonstrated by affinity capture of duplex DNAs by using biotinylated oligonucleotides and streptavidin-covered magnetic beads. The type of complex formed by PNAs, an oligonucleotide and duplex DNA we describe, opens ways for development of various in vitro and in situ hybridization techniques with duplex DNA and may find applications in DNA nanotechnology and genomics.
借助一种DNA合成模拟物——肽核酸(PNA),双链DNA与寡核苷酸之间可组装形成稳定的复合物。已知同嘧啶PNA会侵入双链DNA中的短同嘌呤序列,形成P环。我们发现,在同一DNA链上由混合嘌呤 - 嘧啶序列隔开的两个紧密相邻的嘌呤序列处形成的P环会合并并打开它们之间的双螺旋。未与PNA结合的互补DNA链会暴露出来,并可通过沃森 - 克里克配对与寡核苷酸进行复合。结果,形成了PD环,它由局部开放的双链DNA、PNA“开启器”和寡核苷酸组成。通过使用生物素化寡核苷酸和链霉亲和素包被的磁珠对双链DNA进行亲和捕获,证明了PD环的稳定性和序列特异性。我们所描述的由PNA、寡核苷酸和双链DNA形成的复合物类型,为开发各种用于双链DNA的体外和原位杂交技术开辟了道路,并可能在DNA纳米技术和基因组学中得到应用。