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Stable Domain Assembly of a Monomolecular DNA Quadruplex: Implications for DNA-Based Nanoswitches

机译:单分子DNA四链体的稳定域组装:对基于DNA的纳米开关的影响。

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摘要

In the presence of K+ ions, the 50-GGGTGGGTGGGTGGG-30 (G3T) sequence folds into a monomolecular quadruplex with unusually high thermal stability and unique optical properties. In this study we report that although single G3T molecules unfold and fold rapidly with overlapping melting and refolding curves, G3T multimers (G3T units covalently attached to each other) demonstrate highly reproducible hysteretic behavior. We demonstrate that this behavior necessitates full-length tandem G3T monomers directly conjugated to each other. Any modification of the tandem sequences eliminates the hysteresis. The experimentally measured kinetic parameters and equilibrium transition profiles suggest a highly specific two-state transition in which the folding and unfolding of the first G3T monomer is rate-limiting for both annealing and melting processes. The highly reproducible hysteretic behavior of G3T multimers has the potential to be used in the design of heat-stimulated DNA switches or transistors.
机译:在存在K +离子的情况下,50-GGGTGGGTGGGGGTGGG-30(G3T)序列折叠成具有异常高的热稳定性和独特的光学性质的单分子四链体。在这项研究中,我们报道,尽管单个G3T分子以重叠的解链和再折叠曲线快速展开和折叠,但G3T多聚体(共价连接的G3T单元)表现出高度可重复的滞后行为。我们证明这种行为需要全长串联G3T单体彼此直接共轭。串联序列的任何修饰都消除了滞后现象。实验测得的动力学参数和平衡转变曲线表明,存在高度特异性的二态转变,其中第一G3T单体的折叠和展开对于退火和熔融过程均是限速的。 G3T多聚体的高度可重复的磁滞行为具有潜力,可用于热刺激DNA开关或晶体管的设计。

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