Kandimalla E R, Agrawal S
Hybridon, Inc., Worcester, Massachusetts 01605, USA.
Biochemistry. 1996 Dec 3;35(48):15332-9. doi: 10.1021/bi961505y.
DNA oligonucleotide sequences containing two parallel complementary strands attached through 3'-3' and 5'-5' linkages were synthesized. These oligonucleotides from Hoogsteen base-paired parallel-stranded (PS) hairpin duplexes under appropriate conditions [Kandimalla, E. R., Agrawal, S., Venkataraman, G., & Sasisekharan, V. (1995a) J. Am. Chem. Soc. 117, 6416-6417]. UV melting experiments show that these Hoogsteen hairpin duplexes have a lower thermal stability than that of the Watson-Crick (WC) hairpin duplex (antiparallel) of the same sequence. The circular dichroism (CD) spectrum of the Hoogsteen duplex is different from the canonical B-DNA WC duplex spectrum. The formation of the Hoogsteen duplex is pH-dependent since protonation of cytosine requires lower pH conditions. Studies with oligonucleotides of different loop sizes revel that three- and two-base loops are optimum for the formation of stable Hoogsteen duplexes with 3'-3' and 5'-5' linkages, respectively. The guanine residues in the loop stabilize the duplex as a result of G-G interactions as confirmed by molecular modeling studies. The new PS Hoogsteen duplexes form stable triplexes with complementary (antiparallel to the purine domain) single-stranded RNA and DNA pyrimidine sequences in Py.Pu:Py (pyrimidine third strand-purine WC strand:pyrimidine WC strand) motif. The thermal stability of the resulting triplexes is much higher than that of the conventional triplex (binding of a Hoogsteen pyrimidine third strand to a WC duplex) of the same sequence. The CD spectra of the new triplexes are similar to those of conventional triplexes, suggesting that no conformational change occurs as a result of 3'-3' or 5'-5' linkage. A molecular modeling study was carried out to examine the stereochemical feasibility of the Hoogsteen duplexes and formation of triplexes with single-stranded pyrimidine complementary strands.
合成了包含两条通过3'-3'和5'-5'连接相连的平行互补链的DNA寡核苷酸序列。在适当条件下,这些寡核苷酸形成了Hoogsteen碱基配对的平行链(PS)发夹双链体[坎迪马拉,E. R.,阿格拉瓦尔,S.,文卡塔拉曼,G.,& 萨西克哈兰,V.(1995a)《美国化学会志》117,6416 - 6417]。紫外熔解实验表明,这些Hoogsteen发夹双链体的热稳定性低于相同序列的沃森 - 克里克(WC)发夹双链体(反平行)。Hoogsteen双链体的圆二色性(CD)光谱不同于经典的B - DNA WC双链体光谱。Hoogsteen双链体的形成依赖于pH值,因为胞嘧啶的质子化需要较低的pH条件。对不同环大小的寡核苷酸的研究表明,三碱基环和二碱基环分别最适合形成具有3'-3'和5'-5'连接的稳定Hoogsteen双链体。分子建模研究证实,环中的鸟嘌呤残基由于G - G相互作用而稳定了双链体。新的PS Hoogsteen双链体与互补的(与嘌呤结构域反平行)单链RNA和DNA嘧啶序列在Py.Pu:Py(嘧啶第三链 - 嘌呤WC链:嘧啶WC链)基序中形成稳定的三链体。所得三链体的热稳定性远高于相同序列的传统三链体(Hoogsteen嘧啶第三链与WC双链体的结合)。新三链体的CD光谱与传统三链体的相似,表明3'-3'或5'-5'连接不会导致构象变化。进行了分子建模研究以检验Hoogsteen双链体的立体化学可行性以及与单链嘧啶互补链形成三链体的情况。