Clarendon Laboratory, Department of Physics, University of Oxford, Parks Road, Oxford, OX1 3PU, UK.
Imperial College Centre for Synthetic Biology and Department of Bioengineering, Prince Consort Road, Imperial College London, London, SW7 2AZ, UK.
Nat Commun. 2020 May 22;11(1):2562. doi: 10.1038/s41467-020-16353-y.
Recent years have seen great advances in the development of synthetic self-assembling molecular systems. Designing out-of-equilibrium architectures, however, requires a more subtle control over the thermodynamics and kinetics of reactions. We propose a mechanism for enhancing the thermodynamic drive of DNA strand-displacement reactions whilst barely perturbing forward reaction rates: the introduction of mismatches within the initial duplex. Through a combination of experiment and simulation, we demonstrate that displacement rates are strongly sensitive to mismatch location and can be tuned by rational design. By placing mismatches away from duplex ends, the thermodynamic drive for a strand-displacement reaction can be varied without significantly affecting the forward reaction rate. This hidden thermodynamic driving motif is ideal for the engineering of non-equilibrium systems that rely on catalytic control and must be robust to leak reactions.
近年来,在合成自组装分子系统的发展方面取得了重大进展。然而,设计非平衡结构需要对反应的热力学和动力学进行更精细的控制。我们提出了一种增强 DNA 链置换反应热力学驱动力的机制,同时几乎不影响正向反应速率:在初始双链体中引入错配。通过实验和模拟的结合,我们证明了置换速率对错配位置非常敏感,并且可以通过合理的设计进行调整。通过将错配放置在双链体的末端之外,可以在不显著影响正向反应速率的情况下改变链置换反应的热力学驱动力。这种隐藏的热力学驱动模式非常适合依赖催化控制的非平衡系统的工程设计,并且必须对泄漏反应具有鲁棒性。