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Silver(I)‐mediated hetero base pairs of 6‐pyrazolylpurine and its deaza derivatives
Zeitschrift für anorganische und allgemeine Chemie ( IF 1.1 ) Pub Date : 2021-01-27 , DOI: 10.1002/zaac.202000481
Daniela Escher 1 , Jens Müller 2
Affiliation  

A series of antiparallel‐stranded and parallel‐stranded DNA duplexes containing hetero base pairs of the artificial nucleobases 6‐(1H‐pyrazol‐1‐yl)‐9H‐purine (6PP), 1‐deaza‐6PP (1D6PP), 7‐deaza‐6PP (7D6PP), and 1,7‐dideaza‐6PP (1,7D6PP) were investigated with respect to their ability to form silver(I)‐mediated base pairs. A close examination of the duplex melting temperatures in the absence and in the presence of silver(I) ions shows a strong sequence‐dependence of the stability of the resulting silver(I)‐mediated base pairs. The most stable silver(I)‐mediated base pairs are formed when 1,7D6PP is located in a purine‐rich strand opposite either 6PP or 7D6PP. This indicates that the silver(I) ions are coordinated via the Watson‐Crick edge of the latter nucleobase, whereas they bind to the pyrazolyl moiety of the former. As a result, a [2+1] coordination environment is proposed for the silver(I) ions.

中文翻译:

银(I)介导的6-吡唑基嘌呤及其deaza衍生物的杂碱基对

一系列的反平行链和平行链DNA双链体,包含人工核碱基6-(1 H-吡唑-1-基)-9 H-嘌呤(6PP),1-脱氮基-6PP(1D 6PP)的杂碱基对分别研究了7-deaza-6PP(7D 6PP)和1,7-dideaza-6PP(1,7D 6PP)形成银(I)介导的碱基对的能力。在不存在和存在银(I)离子的情况下,仔细检查双链体的熔化温度可发现所得银(I)介导的碱基对的稳定性与序列的依赖性很大。当1,7D 6PP位于与6PP或7D相对的富嘌呤链中时,形成最稳定的银(I)介导的碱基对6PP。这表明银(I)离子通过后者核碱基的沃森-克里克边进行配位,而它们与前者的吡唑基部分结合。结果,提出了银(I)离子的[2 + 1]配位环境。
更新日期:2021-03-11
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