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Selective, controllable, and reversible aggregation of polystyrene latex microspheres via DNA hybridization
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
Affiliation:Physics Department, California Polytechnic State University, San Luis Obispo, California 93407, USA.
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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