A new building block for DNA network formation by self-assembly and polymerase chain reaction

被引:7
作者
Busskamp, Holger
Keller, Sascha
Robotta, Marta
Drescher, Malte
Marx, Andreas [1 ]
机构
[1] Univ Konstanz, Dept Chem, D-78457 Constance, Germany
关键词
AFM; branched DNA; DNA; DNA polymerase; nanotechnology; nucleic acids; PCR; self-assembly; ATOMIC-FORCE MICROSCOPY; NUCLEIC-ACIDS; BRANCHED DNA; PULSED EPR; IN-VIVO; CONSTRUCTION; OLIGONUCLEOTIDES; NANOSTRUCTURES; DESIGN; NANOARCHITECTURES;
D O I
10.3762/bjoc.10.104
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
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.
引用
收藏
页码:1037 / 1046
页数:10
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