DNA Regulated Clusters: Structure and Self-limiting Assembly

ORAL

Abstract

We have investigated the structural details of nanoparticle clusters assembled by flexible DNA linkers in dimer clusters using electron microscopy, in-situ x-ray scattering and optical methods. The observed dependence of interparticle distance on a DNA length significantly deviates from the predictions for single chain linkages and previous measurements for superlattices. The observed effect is attributed to a large solid angle of interparticle contact, in agreement with computational results. Our studies further reveal the non-monotonic decrease of interparticle distance for the longer linkers; that suggests nanoparticles confinement by hybridized linkers from opposite particles' hemispheres. The effect is accompanied by inhibited development of nanoclusters and results in a self-limited cluster assembly. The mechanism of dimer formation was investigated in details using the optical methods.

*Research was supported by the U.S. Department of Energy, Office of Basic Energy Sciences, under Contract No. DE-AC02-98CH10886.

Authors

  • Ching-Jung Cheng

    • Center for Functional Nanomaterials, Brookhaven National Laboratory
    • Center for Functional Nanomaterials, Brookhaven National Laboratory, Upton, NY
  • Fernando Vargas Lara

    • Physics Department, Wesleyan University
  • Francis Starr

    • Physics Department, Wesleyan University
  • Alexei Tkachenko

    • Center for Functional Nanomaterials, Brookhaven National Laboratory
  • Oleg Gang

    • Center for Functional Nanomaterials, Brookhaven National Laboratory
    • Brookhaven National Laboratory
    • Center for Functional Nanomaterials, Brookhaven National Laboratory, Upton, NY