Slocombe Louie, Winokan Max, Al-Khalili Jim, Sacchi Marco
Leverhulme Quantum Biology Doctoral Training Centre, University of Surrey, Guildford, GU2 7XH, UK.
Department of Chemistry, University of Surrey, Guildford, GU2 7XH, UK.
Commun Chem. 2022 Nov 5;5(1):144. doi: 10.1038/s42004-022-00760-x.
Proton transfer between the DNA bases can lead to mutagenic Guanine-Cytosine tautomers. Over the past several decades, a heated debate has emerged over the biological impact of tautomeric forms. Here, we determine that the energy required for generating tautomers radically changes during the separation of double-stranded DNA. Density Functional Theory calculations indicate that the double proton transfer in Guanine-Cytosine follows a sequential, step-like mechanism where the reaction barrier increases quasi-linearly with strand separation. These results point to increased stability of the tautomer when the DNA strands unzip as they enter the helicase, effectively trapping the tautomer population. In addition, molecular dynamics simulations indicate that the relevant strand separation time is two orders of magnitude quicker than previously thought. Our results demonstrate that the unwinding of DNA by the helicase could simultaneously slow the formation but significantly enhance the stability of tautomeric base pairs and provide a feasible pathway for spontaneous DNA mutations.
DNA碱基之间的质子转移可导致诱变的鸟嘌呤 - 胞嘧啶互变异构体。在过去几十年里,关于互变异构形式的生物学影响出现了激烈的争论。在这里,我们确定在双链DNA分离过程中产生互变异构体所需的能量会发生根本性变化。密度泛函理论计算表明,鸟嘌呤 - 胞嘧啶中的双质子转移遵循一种连续的、阶梯状机制,其中反应势垒随链分离呈准线性增加。这些结果表明,当DNA链在进入解旋酶时解开时,互变异构体的稳定性增加,有效地捕获了互变异构体群体。此外,分子动力学模拟表明,相关的链分离时间比之前认为的快两个数量级。我们的结果表明,解旋酶解开DNA的过程可能同时减缓互变异构碱基对的形成,但显著增强其稳定性,并为自发的DNA突变提供了一条可行的途径。