Institut für Anorganische und Analytische Chemie, Universität Münster, Corrensstr. 30, 48149, Münster, Germany.
Center for Soft Nanoscience (SoN) and Cells in Motion Interfaculty Centre (CiMIC), Universität Münster, Corrensstr. 30, 48149, Münster, Germany.
J Biol Inorg Chem. 2023 Dec;28(8):791-803. doi: 10.1007/s00775-023-02022-0. Epub 2023 Nov 20.
The artificial nucleobase 6-pyrazolylpurine (6PP) and its deaza derivatives 1-deaza-6-pyrazolylpurine (6PP), 7-deaza-6-pyrazolylpurine (6PP), and 1,7-dideaza-6-pyrazolylpurine (6PP) were investigated with respect to their ability to differentiate between the canonical nucleobases cytosine and thymine by means of silver(I)-mediated base pairing. As shown by temperature-dependent UV spectroscopy and by circular dichroism spectroscopy, 6PP and (to a lesser extent) 6PP form stable silver(I)-mediated base pairs with cytosine, but not with thymine. 6PP and 6PP do not engage in the formation of stabilizing silver(I)-mediated base pairs with cytosine or thymine. The different behavior of 6PP, 6PP, and 6PP indicates that silver(I) binding occurs via the N1 position of the purine derivative, i.e. via the Watson-Crick face. The data show that 6PP is capable of differentiating between cytosine and thymine, which is potentially relevant in the context of detecting single-nucleotide polymorphisms.
研究了人工核苷碱基 6-吡唑基嘌呤(6PP)及其去氮衍生物 1-脱氮-6-吡唑基嘌呤(6PP)、7-脱氮-6-吡唑基嘌呤(6PP)和 1,7-二脱氮-6-吡唑基嘌呤(6PP)与银(I)介导的碱基配对区分 canonical 碱基胞嘧啶和胸腺嘧啶的能力。如温度依赖性紫外光谱和圆二色性光谱所示,6PP 和(在较小程度上)6PP 与胞嘧啶形成稳定的银(I)介导的碱基对,但与胸腺嘧啶不形成。6PP 和 6PP 不与胞嘧啶或胸腺嘧啶形成稳定的银(I)介导的碱基对。6PP、6PP 和 6PP 的不同行为表明,银(I)结合发生在嘌呤衍生物的 N1 位置,即通过 Watson-Crick 面。数据表明,6PP 能够区分胞嘧啶和胸腺嘧啶,这在检测单核苷酸多态性方面具有潜在意义。