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Helix-Forming Properties of Size-Expanded DNA,an Alternative Four-Base Genetic Form

机译:大小扩展的DNA,另一种四碱基遗传形式的螺旋形成特性。

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摘要

We describe the chemical and biophysical characterization of a new four-base genetic system,in which all base pairs are larger than the natural pairs.A recent preliminary study showed that three sequences containing size-expanded DNA(xDNA)bases could form stable cooperative complexes.However,many of the standard and essential properties that natural DNA possesses were unexplored for this new class of helical assembly.We therefore undertook a study of several properties of this new genetic complex:strand stoichiometry,preferred strand polarity(i.e.,parallel vs antiparallel),mismatch selectivity,base size selectivity,ionic strength dependence,fluorescence behavior,CD spectra,and sequence generality.Results showed that several sequences formed double-stranded helical complexes,and interestingly,a pyrimidine-rich strand of xDNA bases was shown to form a triple helical complex as well.A test of strand polarity showed a preference for antiparallel orientation,as does natural DNA.Mismatch and size selectivity were generally moderate to strong,with one exception.Ionic strength dependence varied by relatively small degrees from that of natural DNA,although a triple helical complex of xDNA showed more marked dependence.Spectral characteristics(fluorescence,CD)were found to be quite different than those of natural DNA,apparently because of large differences in the electronic character of the expanded pi-systems.Finally,several sequence contexts were found to form helices in a sequence-predictable manner.Two exceptions were noted and may be explained by competition from alternative folding structures and/or strong,single-stranded stacking.The viability of xDNA as an alternative genetic system and its possible biotechnological applications are discussed.
机译:我们描述了一个新的四碱基遗传系统的化学和生物物理特征,该系统的所有碱基对均大于自然碱基对。最近的一项初步研究表明,三个包含大小扩展的DNA(xDNA)碱基的序列可以形成稳定的合作复合体然而,对于这种新型的螺旋装配,天然DNA所具有的许多标准特性和基本特性尚未得到开发。因此,我们对这种新型遗传复合物的几种特性进行了研究:链化学计量,优选链极性(即,平行与反平行) ),错配选择性,碱基大小选择性,离子强度依赖性,荧光行为,CD光谱和序列通用性。结果显示,多个序列形成了双链螺旋复合物,有趣的是,显示了一条富含嘧啶的xDNA碱基链链极性的测试表明,与天然DNA一样,它倾向于反平行取向,天然DNA也是如此。大小选择性一般为中等至强,但有一个例外。离子强度的依赖性与天然DNA的依赖性变化较小,尽管xDNA的三螺旋复合物表现出更明显的依赖性。发现光谱特征(荧光,CD)相当不同于天然DNA,显然是因为扩展的pi系统的电子特性差异很大。最后,发现了多个序列上下文以序列可预测的方式形成了螺旋。注意到了两个例外,可以通过竞争来解释讨论了xDNA作为替代遗传系统的可行性及其可能的生物技术应用。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2005年第5期|p.1396-1402|共7页
  • 作者单位

    Contribution from the Department of Chemistry,Stanford University,Stanford,California 94305-5080;

    Contribution from the Department of Chemistry,Stanford University,Stanford,California 94305-5080;

    Contribution from the Department of Chemistry,Stanford University,Stanford,California 94305-5080;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

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