DNA-Driven Assembly: From Polyhedral Nanoparticles to Proteins

Martin Girard, Jaime A. Millan, Monica Olvera De La Cruz

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

Abstract

Directed crystallization of a large variety of nanoparticles, including proteins, via DNA hybridization kinetics has led to unique materials with a broad range of crystal symmetries. The nanoparticles are functionalized with DNA chains that link neighboring functionalized units. The shape of the nanoparticle, the DNA length, the sequence of the hybridizing DNA linker, and the grafting density determine the crystal symmetries and lattice spacing. By carefully selecting these parameters, one can, in principle, achieve all the symmetries found for both atomic and colloidal crystals of asymmetric shapes as well as new symmetries and can drive transitions between them. A scale-accurate coarse-grained model with explicit DNA chains provides the design parameters, including the degree of hybridization, to achieve specific crystal structures. The model also provides surface energy values to determine the shape of defect-free single crystals with macroscopic anisotropic properties, which has potential for the fabrication of materials with specific optical and mechanical properties.

Original languageEnglish (US)
Pages (from-to)33-49
Number of pages17
JournalAnnual Review of Materials Research
Volume47
DOIs
StatePublished - Jul 3 2017

Keywords

  • DNA
  • Molecular dynamics
  • Nanoparticle
  • Proteins
  • Self-assembly

ASJC Scopus subject areas

  • Materials Science(all)

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