首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Photochemical selectivity in guanine-cytosine base-pair structures.
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Photochemical selectivity in guanine-cytosine base-pair structures.

机译:鸟嘌呤-胞嘧啶碱基对结构中的光化学选择性。

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摘要

Prebiotic chemistry presumably took place before formation of an oxygen-rich atmosphere and thus under conditions of intense short wavelength UV irradiation. Therefore, the UV photochemical stability of the molecular building blocks of life may have been an important selective factor in determining the eventual chemical makeup of critical biomolecules. To investigate the role of UV irradiation in base-pairing we have studied guanine (G) and cytosine (C) base pairs in the absence of the RNA backbone. We distinguished base-pair structures by IR-UV hole-burning spectroscopy as well as by high-level correlated ab initio calculations. The Watson-Crick structure exhibits broad UV absorption, in stark contrast to other GC structures and other base-pair structures. This broad absorption may be explained by a rapid internal conversion that makes this specific base pair arrangement uniquely photochemically stable.
机译:益生元化学大概是在形成富氧气氛之前发生的,因此发生在强烈的短波紫外线辐射条件下。因此,生命分子组成部分的紫外线光化学稳定性可能已成为决定关键生物分子最终化学组成的重要选择因素。为了研究紫外线照射在碱基配对中的作用,我们研究了在没有RNA主链的情况下鸟嘌呤(G)和胞嘧啶(C)碱基对。我们通过IR-UV空穴燃烧光谱以及高级相关的从头算算来区分碱基对结构。与其他GC结构和其他碱基对结构形成鲜明对比的是,Watson-Crick结构具有广泛的紫外线吸收能力。这种广泛的吸收可以用快速的内部转化来解释,这种快速的内部转化使这种特定的碱基对排列独特地具有光化学稳定性。

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