Chemistries for DNA Nanotechnology

被引:319
|
作者
Madsen, Mikael [1 ,2 ]
Gothelf, Kurt V. [1 ,2 ]
机构
[1] Aarhus Univ, Interdisciplinary Nanosci Ctr iNANO, Gustav Wieds Vej 14, DK-8000 Aarhus C, Denmark
[2] Aarhus Univ, Dept Chem, Gustav Wieds Vej 14, DK-8000 Aarhus C, Denmark
基金
新加坡国家研究基金会;
关键词
RESONANCE ENERGY-TRANSFER; PEPTIDE NUCLEIC-ACIDS; SOLID-PHASE SYNTHESIS; FUNCTIONALIZED GOLD NANOPARTICLES; SINGLE-MOLECULE FLUORESCENCE; TEMPLATED ORGANIC-SYNTHESIS; SHAPE-CONTROLLED SYNTHESIS; ZINC-FINGER PROTEINS; PHOTO-CROSS-LINKING; QUANTUM DOTS;
D O I
10.1021/acs.chemrev.8b00570
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The predictable nature of DNA interactions enables the programmable assembly of highly advanced 2D and 3D DNA structures of nanoscale dimensions. The access to ever larger and more complex structures has been achieved through decades of work on developing structural design principles. Concurrently, an increased focus has emerged on the applications of DNA nanostructures. In its nature, DNA is chemically inert and nanostructures based on unmodified DNA mostly lack function. However, functionality can be obtained through chemical modification of DNA nanostructures and the opportunities are endless. In this review, we discuss methodology for chemical functionalization of DNA nanostructures and provide examples of how this is being used to create functional nanodevices and make DNA nanostructures more applicable. We aim to encourage researchers to adopt chemical modifications as part of their work in DNA nanotechnology and inspire chemists to address current challenges and opportunities within the field.
引用
收藏
页码:6384 / 6458
页数:75
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