Megger Dominik A, Muller Jens
Westfalische Wilhelms-Universitat Munster, Institut fur Anorganische und Analytische Chemie, Munster, Germany.
Nucleosides Nucleotides Nucleic Acids. 2010 Jan;29(1):27-38. doi: 10.1080/15257770903451579.
A 2'-deoxyribonucleoside containing 1,3-dideaza-6-nitropurine was synthesized and incorporated into oligonucleotides. The acid-base properties of this nucleoside and the corresponding N9-methylated derivative were investigated by pD-dependent (1)H NMR spectroscopy. A possible formation of Hoogsteen-type base pairs with cytosine was studied by ultraviolet (UV) and circular dichroism (CD) spectroscopy in the presence and absence of Ag(I) and under neutral and acidic conditions, respectively. In each case, no indication for the formation of Hoogsteen-type base pairs was obtained, which is attributed to the higher affinity of cytosine to form self-complementary hemi-protonated base pairs under acidic conditions and metal-mediated homo base pairs in presence of Ag(I), respectively.
合成了一种含有1,3 - 二脱氮 - 6 - 硝基嘌呤的2'-脱氧核糖核苷,并将其掺入寡核苷酸中。通过pD依赖的¹H NMR光谱研究了该核苷及其相应的N9 - 甲基化衍生物的酸碱性质。分别在中性和酸性条件下,在有和没有Ag(I)存在的情况下,通过紫外(UV)和圆二色性(CD)光谱研究了与胞嘧啶形成Hoogsteen型碱基对的可能性。在每种情况下,均未获得形成Hoogsteen型碱基对的迹象,这分别归因于胞嘧啶在酸性条件下形成自互补半质子化碱基对以及在Ag(I)存在下形成金属介导的同型碱基对的亲和力更高。