Limiting the valence: advancements and new perspectives on patchy colloids, soft functionalized nanoparticles and biomolecules
arXiv:1705.04383 · doi:10.1039/C7CP03149A
Abstract
Limited bonding valence, usually accompanied by well-defined directional interactions and selective bonding mechanisms, is nowadays considered among the key ingredients to create complex structures with tailored properties: even though isotropically interacting units already guarantee access to a vast range of functional materials, anisotropic interactions can provide extra instructions to steer the assembly of specific architectures. The anisotropy of effective interactions gives rise to a wealth of self-assembled structures both in the realm of suitably synthesized nano- and micro-sized building blocks and in nature, where the isotropy of interactions is often a zero-th order description of the complicated reality. In this review, we span a vast range of systems characterized by limited bonding valence, from patchy colloids of new generation to polymer-based functionalized nanoparticles, DNA-based systems and proteins, and describe how the interaction patterns of the single building blocks can be designed to tailor the properties of the target final structures.
References in corpus (22)
- Motility-Induced Phase Separation
- Physics of Microswimmers - Single Particle Motion and Collective Behavior
- Phase diagram of patchy colloids: towards empty liquids
- Induced-charge Electrophoresis of Metallo-dielectric Particles
- Mechanisms of virus assembly
- Crucial role of non-specific interactions in amyloid nucleation
- Role of reversibility in viral capsid growth: A paradigm for self-assembly
- Mobile linkers on DNA-coated colloids: valency without patches
- Phase diagrams of binary mixtures of patchy colloids with distinct numbers of patches: The network fluid regime
- Self-assembly of "Mickey Mouse" shaped colloids into tube-like structures: experiments and simulations
- Self-assembly of short DNA duplexes: from a coarse-grained model to experiments through a theoretical link
- Interaction of charged patchy protein models with like-charged polyelectrolyte brushes
- Fabrication of polyhedral particles from spherical colloids and their self-assembly into rotator phases
- Symmetry effects in electrostatic interactions between two arbitrarily charged spherical shells in the Debye-Hückel approximation
- Transferable coarse-grained potential for protein folding and design
- Effective stiffness and formation of secondary structures in a protein-like model
- Theoretical and numerical investigations of inverse patchy colloids in the fluid phase
- Self-assembly of DNA-functionalized colloids
- Emergent rhombus tilings from molecular interactions with -fold rotational symmetry
- Controlling the folding and substrate-binding of proteins using polymer brushes
- Competition between monomeric and dimeric crystals in schematic models for globular proteins
- Equilibrium adsorption and self-assembly of patchy colloids in microchannels