School of Physics, Georgia Institute of Technology, 837 State Street, Atlanta, Georgia 30332-0430, USA.
Phys Rev Lett. 2019 May 31;122(21):218101. doi: 10.1103/PhysRevLett.122.218101.
Base-pair mismatch can relieve mechanical stress in highly strained DNA molecules, but how it affects their kinetic stability is not known. Using single-molecule fluorescence resonance energy transfer, we measured the lifetimes of tightly bent DNA loops with and without base-pair mismatch. Surprisingly, for loops captured by stackable sticky ends which leave single-stranded DNA breaks (or nicks) upon annealing, the mismatch decreased the loop lifetime despite reducing the overall bending stress, and the decrease was largest when the mismatch was placed at the DNA midpoint. These findings suggest that base-pair mismatch increases bending stress at the opposite side of the loop through an allosteric mechanism known as cooperative kinking. Based on this mechanism, we present a three-state model that explains the apparent dichotomy between thermodynamic and kinetic stability.
碱基对错配可以减轻高度应变 DNA 分子中的机械应力,但它如何影响其动力学稳定性尚不清楚。使用单分子荧光共振能量转移,我们测量了带有和不带有碱基对错配的紧密弯曲 DNA 环的寿命。令人惊讶的是,对于由可堆叠粘性末端捕获的环,这些粘性末端在退火时会留下单链 DNA 断裂(或缺口),尽管错配降低了整体弯曲应力,但错配放置在 DNA 中点时,环的寿命下降最大。这些发现表明,碱基对错配通过一种称为协同扭结的变构机制在环的相反侧增加弯曲应力。基于这个机制,我们提出了一个三状态模型,解释了热力学和动力学稳定性之间的明显二分法。