Linker-mediated self-assembly of mobile DNA-coated colloids
arXiv:1908.04068 · doi:10.1126/sciadv.aaz6921
Abstract
Developing construction methods of materials tailored for given applications with absolute control over building block placement poses an immense challenge. DNA-coated colloids offer the possibility of realising programmable self-assembly, which, in principle, can assemble almost any structure in equilibrium, but remains challenging experimentally. Here, we propose an innovative system of linker-mediated mobile DNA-coated colloids (mDNACCs), in which mDNACCs are bridged by the free DNA linkers in solution, whose two single-stranded DNA tails can bind with specific single-stranded DNA receptors of complementary sequence coated on colloids. We formulate a mean-field theory efficiently calculating the effective interaction between mDNACCs, where the entropy of DNA linkers plays a nontrivial role. Particularly, when the binding between free DNA linkers in solution and the corresponding receptors on mDNACCs is strong, the linker-mediated colloidal interaction is determined by the linker entropy depending on the linker concentration.
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Cited by in corpus (9)
- Entropy-Controlled Cross-Linking in Linker-Mediated Vitrimers
- A Coarse-Grained Simulation Model for Self-Assembly of Liquid Droplets Featuring Explicit Mobile Binders
- Entropy driven thermo-gelling vitrimer
- Percolation in binary mixtures of linkers and particles: chaining {\it {vs}} branching
- Dynamics of equilibrium linked colloidal gels
- Designing superselectivity in linker-mediated multivalent nanoparticle adsorption
- Coarse-grained dynamics of transiently-bound fast linkers
- A bond swap algorithm for simulating dynamically crosslinked polymers
- Designed self-assembly of programmable colloidal atom-electron equivalents