Journal
PHYSICAL CHEMISTRY CHEMICAL PHYSICS
Volume 25, Issue 11, Pages 7847-7858Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d2cp04683k
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The uniqueness of DNA sequence specificity makes it an ideal building block for constructing precise and accurate nanoscale arrays and devices. In this study, DNA nanostars with three, four, and five arms were self-assembled into a gel phase using a simplified bead-spring model. Simulations showed that the DNA nanostars formed a thermodynamically stable gel phase from an unstructured liquid phase at lower temperatures. The phase transition was characterized by calculating various structural features and quantifying the thermodynamics of gelation.
The unique sequence specificity rule of DNA makes it an ideal molecular building block for constructing periodic arrays and devices with nanoscale accuracy and precision. Here, we present the self-assembly of DNA nanostars having three, four and five arms into a gel phase using a simplistic coarse-grained bead-spring model developed by Z. Xing, C. Ness, D. Frenkel and E. Eiser (Macromolecules, 2019, 52, 504-512). Our simulations show that the DNA nanostars form a thermodynamically stable fully bonded gel phase from an unstructured liquid phase with the lowering of temperature. We characterize the phase transition by calculating several structural features such as the radial distribution function and structure factor. The thermodynamics of gelation is quantified by the potential energy and translational pair-entropy of the system. The phase transition from an arrested gel phase to an unstructured liquid phase has been modelled using a two-state theoretical model. We find that this transition is enthalpy driven, and loss of configuration and translational entropy is counterpoised by enthalpic interaction of the DNA sticky-ends, which gives rise to a gel phase at low temperature. The absolute rotational and translational entropy of the systems, measured using a two-phase thermodynamic model, also substantiates the gel transition. The slowing down of the dynamics upon approaching the transition temperature from a high temperature demonstrates the phase transition to a gel phase. A detailed numerical simulation study of the morphology, dynamics and thermodynamics of DNA gelation can provide guidance for future experiments, is easily extensible to other polymeric systems, and is expected to help in understanding the physics of self-assembly.
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