Selective, controllable, and reversible aggregation of polystyrene latex microspheres via DNA hybridization |
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Authors: | Rogers Phillip H Michel Eric Bauer Carl A Vanderet Stephen Hansen Daniel Roberts Bradley K Calvez Antoine Crews Jackson B Lau Kwok O Wood Alistair Pine David J Schwartz Peter V |
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Affiliation: | Physics Department, California Polytechnic State University, San Luis Obispo, California 93407, USA. |
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Abstract: | The directed three-dimensional self-assembly of microstructures and nanostructures through the selective hybridization of DNA is the focus of great interest toward the fabrication of new materials. Single-stranded DNA is covalently attached to polystyrene latex microspheres. Single-stranded DNA can function as a sequence-selective Velcro by only bonding to another strand of DNA that has a complementary sequence. The attachment of the DNA increases the charge stabilization of the microspheres and allows controllable aggregation of microspheres by hybridization of complementary DNA sequences. In a mixture of microspheres derivatized with different sequences of DNA, microspheres with complementary DNA form aggregates, while microspheres with noncomplementary sequences remain suspended. The process is reversible by heating, with a characteristic "aggregate dissociation temperature" that is predictably dependent on salt concentration, and the evolution of aggregate dissociation with temperature is observed with optical microscopy. |
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