Letter abstract


Nature Materials 8, 590 - 595 (2009)
Published online: 14 June 2009 | doi:10.1038/nmat2471

Subject Categories: Colloids | Biological materials | Nanoscale materials

Switchable self-protected attractions in DNA-functionalized colloids

Mirjam E. Leunissen1, Rémi Dreyfus1, Fook Chiong Cheong1, David G. Grier1, Roujie Sha2, Nadrian C. Seeman2 & Paul M. Chaikin1

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Surface functionalization with DNA is a powerful tool for guiding the self-assembly of nanometre- and micrometre-sized particles1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11. Complementary 'sticky ends' form specific inter-particle links and reproducibly bind at low temperature and unbind at high temperature. Surprisingly, the ability of single-stranded DNA to form folded secondary structures has not been explored for controlling (nano) colloidal assembly processes, despite its frequent use in DNA nanotechnology12, 13, 14. Here, we show how loop and hairpin formation in the DNA coatings of micrometre-sized particles gives us in situ control over the inter-particle binding strength and association kinetics. We can finely tune and even switch off the attractions between particles, rendering them inert unless they are heated or held together—like a nano-contact glue. The novel kinetic control offered by the switchable self-protected attractions is explained with a simple quantitative model that emphasizes the competition between intra- and inter-particle hybridization, and the practical utility is demonstrated by the assembly of designer clusters in concentrated suspensions. With self-protection, both the suspension and assembly product are stable, whereas conventional attractive colloids would quickly aggregate. This remarkable functionality makes our self-protected colloids a novel material that greatly extends the utility of DNA-functionalized systems, enabling more versatile, multi-stage assembly approaches.

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  1. Center for Soft Matter Research, Physics Department, New York University, 4 Washington Place, New York 10003, USA
  2. Chemistry Department, New York University, 100 Washington Square East, New York 10003, USA

Correspondence to: Mirjam E. Leunissen1 e-mail: m.e.leunissen@nyu.edu



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