Mallajosyula Sairam S, Pati Swapan K
Theoretical Sciences Unit, Jawaharlal Nehru Center for Advanced Scientific Research, Jakkur Campus, Bangalore, India.
J Phys Chem B. 2007 Oct 11;111(40):11614-8. doi: 10.1021/jp076063m. Epub 2007 Sep 20.
Protonation of DNA basepairs is a reversible phenomenon that can be controlled by tuning the pH of the system. Under mild acidic conditions, the hydrogen-bonding pattern of the DNA basepairs undergoes a change. We study the effect of protonation on the electronic properties of the DNA basepairs to probe for possible molecular electronics applications. We find that, under mild acidic pH conditions, the A:T basepair shows excellent rectification behavior that is, however, absent in the G:C basepair. The mechanism of rectification has been discussed using a simple chemical potential model. We also consider the noncanonical A:A basepair and find that it can be used as efficient pH dependent molecular switch. The switching action in the A:A basepair is explained in the light of pi-pi interactions, which lead to efficient delocalization over the entire basepair.
DNA碱基对的质子化是一种可逆现象,可以通过调节系统的pH值来控制。在温和的酸性条件下,DNA碱基对的氢键模式会发生变化。我们研究质子化对DNA碱基对电子性质的影响,以探索可能的分子电子学应用。我们发现,在温和的酸性pH条件下,A:T碱基对表现出优异的整流行为,然而,G:C碱基对中却不存在这种行为。已使用简单的化学势模型讨论了整流机制。我们还考虑了非规范的A:A碱基对,发现它可以用作高效的pH依赖性分子开关。根据π-π相互作用解释了A:A碱基对中的开关作用,这种相互作用导致在整个碱基对上的有效离域。