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三唑-吖啶缀合物:与双链 DNA 相互作用的氧化还原机制和原位电化学评价。

Triazole-acridine conjugates: redox mechanisms and in situ electrochemical evaluation of interaction with double-stranded DNA.

机构信息

Departamento de Química, Faculdade de Ciências e Tecnologia, Universidade de Coimbra, 3004-535 Coimbra, Portugal.

出版信息

Bioelectrochemistry. 2013 Feb;89:50-6. doi: 10.1016/j.bioelechem.2012.08.005. Epub 2012 Sep 11.

Abstract

Redox mechanisms and in situ electrochemical interaction with double-stranded DNA were investigated using a DNA-electrochemical biosensor for two disubstituted triazole-linked acridine compounds (GL15 and GL7), previously reporting as quadruplex DNA-binding molecules. The redox properties of GL15 and GL7 involve a complex, pH-dependent, adsorption-controlled irreversible process and were investigated using cyclic, differential pulse, and square wave voltammetry at a glassy carbon electrode. The interaction between duplex DNA and GL15 or GL7 was investigated in incubated solutions using dsDNA-, poly[G]-, and poly[A]-electrochemical biosensors. It was demonstrated that the interaction is time-dependent, both GL15 and GL7 interacting with dsDNA, causing condensation of dsDNA morphological structure but not oxidative damage.

摘要

使用一种 DNA 电化学生物传感器研究了两种取代的三唑连接吖啶化合物(GL15 和 GL7)的氧化还原机制和与双链 DNA 的原位电化学相互作用,这两种化合物先前被报道为四链体 DNA 结合分子。GL15 和 GL7 的氧化还原性质涉及复杂的、依赖 pH 的、吸附控制的不可逆过程,并在玻碳电极上使用循环伏安法、差分脉冲伏安法和方波伏安法进行了研究。使用双链 DNA-、聚[G]-和聚[A]-电化学生物传感器在孵育溶液中研究了双链 DNA 与 GL15 或 GL7 之间的相互作用。结果表明,这种相互作用是时间依赖性的,GL15 和 GL7 都与 dsDNA 相互作用,导致 dsDNA 形态结构的凝聚,但不会造成氧化损伤。

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