Sugimoto N, Satoh N, Yasuda K, Nakano S
Department of Chemistry, Faculty of Science and Engineering, Konan University, 8-9-1 Okamoto, Higashinada-ku, Kobe 658-8501, Japan.
Biochemistry. 2001 Jul 24;40(29):8444-51. doi: 10.1021/bi010480m.
Peptide nucleic acid (PNA) is an oligonucleotide analogue in which the sugar-phosphate backbone is replaced by an N-(2-aminoethyl)glycine unit to which the nucleobases are attached. We investigated the thermodynamic behavior of PNA/DNA hybrid duplexes with identical nearest neighbors but with different sequences and chain lengths (5, 6, 7, 8, 10, 12, and 16 mers) to reveal whether the nearest-neighbor model is valid for the PNA/DNA duplex stability. CD spectra of 6, 7, and 8 mer PNA/DNA duplexes showed similar signal, while 10, 12, and 16 mer duplexes did not. The average difference in Delta G degrees (37) for short PNA/DNA duplexes with identical nearest-neighbor pairs was only 3.5%, whereas that of longer duplexes (10, 12, and 16 mers) was 16.4%. Therefore, the nearest-neighbor model seems to be useful at least for the short PNA/DNA duplexes. Thermodynamics of PNA/DNA duplexes containing 1--3 bulge residues were also studied. While the stability of the 12 mer DNA/DNA duplex decreased as the number of bulge bases increases, the number of bulge bases in PNA/DNA unchanged the duplex stability. Thus, the influence of bulge insertion in the PNA/DNA duplexes is different from that of a DNA/DNA duplex. This might be due to the different base geometry in a helix which may potentially make hydrogen bonds in a base pair and stacking interaction unfavorable compared with DNA/DNA duplexes.
肽核酸(PNA)是一种寡核苷酸类似物,其中糖磷酸主链被N-(2-氨基乙基)甘氨酸单元取代,核碱基连接在该单元上。我们研究了具有相同最近邻但不同序列和链长(5、6、7、8、10、12和16聚体)的PNA/DNA杂交双链体的热力学行为,以揭示最近邻模型是否对PNA/DNA双链体稳定性有效。6、7和8聚体PNA/DNA双链体的圆二色光谱显示出相似的信号,而10、12和16聚体双链体则没有。具有相同最近邻对的短PNA/DNA双链体的ΔG°(37)平均差异仅为3.5%,而较长双链体(10、12和16聚体)的平均差异为16.4%。因此,最近邻模型似乎至少对短PNA/DNA双链体是有用的。还研究了含有1-3个凸起残基的PNA/DNA双链体的热力学。虽然12聚体DNA/DNA双链体的稳定性随着凸起碱基数量的增加而降低,但PNA/DNA中的凸起碱基数量并未改变双链体稳定性。因此,PNA/DNA双链体中凸起插入的影响与DNA/DNA双链体不同。这可能是由于螺旋中不同的碱基几何形状,与DNA/DNA双链体相比,这可能会使碱基对中的氢键和堆积相互作用变得不利。