@article{Bukamp2014build-28333,
  year={2014},
  doi={10.3762/bjoc.10.104},
  title={A new building block for DNA network formation by self-assembly and polymerase chain reaction},
  volume={10},
  issn={2195-951X},
  journal={Beilstein Journal of Organic Chemistry},
  pages={1037--1046},
  author={Bußkamp, Holger and Keller, Sascha and Robotta, Marta and Drescher, Malte and Marx, Andreas}
}

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    <dc:contributor>Marx, Andreas</dc:contributor>
    <dc:contributor>Bußkamp, Holger</dc:contributor>
    <dc:contributor>Drescher, Malte</dc:contributor>
    <dc:creator>Keller, Sascha</dc:creator>
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    <dc:contributor>Keller, Sascha</dc:contributor>
    <dc:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2014-07-17T09:58:13Z</dc:date>
    <dc:creator>Marx, Andreas</dc:creator>
    <dc:contributor>Robotta, Marta</dc:contributor>
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    <dc:creator>Drescher, Malte</dc:creator>
    <dc:creator>Robotta, Marta</dc:creator>
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    <dcterms:bibliographicCitation>Beilstein Journal of Organic Chemistry ; 10 (2014). - S. 1037-1046</dcterms:bibliographicCitation>
    <dcterms:title>A new building block for DNA network formation by self-assembly and polymerase chain reaction</dcterms:title>
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    <dcterms:abstract xml:lang="eng">The predictability of DNA self-assembly is exploited in many nanotechnological approaches. Inspired by naturally existing self-assembled DNA architectures, branched DNA has been developed that allows self-assembly to predesigned architectures with dimensions on the nanometer scale. DNA is an attractive material for generation of nanostructures due to a plethora of enzymes which modify DNA with high accuracy, providing a toolbox for many different manipulations to construct nanometer scaled objects. We present a straightforward synthesis of a rigid DNA branching building block successfully used for the generation of DNA networks by self-assembly and network formation by enzymatic DNA synthesis. The Y-shaped 3-armed DNA construct, bearing 3 primer strands is accepted by Taq DNA polymerase. The enzyme uses each arm as primer strand and incorporates the branched construct into large assemblies during PCR. The networks were investigated by agarose gel electrophoresis, atomic force microscopy, dynamic light scattering, and electron paramagnetic resonance spectroscopy. The findings indicate that rather rigid DNA networks were formed. This presents a new bottom-up approach for DNA material formation and might find applications like in the generation of functional hydrogels.</dcterms:abstract>
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