Self-Assembling Nucleic Acid Nanostructures Functionalized with Aptamers

被引:110
|
作者
Krissanaprasit, Abhichart [1 ]
Key, Carson M. [2 ]
Pontula, Sahil [3 ,4 ]
LaBean, Thomas H. [1 ]
机构
[1] North Carolina State Univ, Coll Engn, Dept Mat Sci & Engn, Raleigh, NC 27695 USA
[2] Duke Univ, Dept Biomed Engn, Durham, NC 27708 USA
[3] MIT, Dept Phys, Cambridge, MA 02139 USA
[4] MIT, Dept Elect Engn & Comp Sci, Cambridge, MA 02139 USA
基金
美国国家科学基金会;
关键词
ROLLING CIRCLE TRANSCRIPTION; HYBRIDIZATION CHAIN-REACTION; DNA ORIGAMI NANOSTRUCTURES; SHAPE ELECTROCHEMICAL APTASENSOR; TARGETED DRUG-DELIVERY; METHYLENE-BLUE BINDING; CROSS-LINKED HYDROGEL; SINGLE-STRANDED-DNA; IN-VITRO SELECTION; GC BASE SEQUENCE;
D O I
10.1021/acs.chemrev.0c01332
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Researchers have worked for many decades to master the rules of biomolecular design that would allow artificial biopolymer complexes to self-assemble and function similarly to the diverse biochemical constructs displayed in natural biological systems. The rules of nucleic acid assembly (dominated by Watson-Crick base-pairing) have been less difficult to understand and manipulate than the more complicated rules of protein folding. Therefore, nucleic acid nanotechnology has advanced more quickly than de novo protein design, and recent years have seen amazing progress in DNA and RNA design. By combining structural motifs with aptamers that act as affinity handles and add powerful molecular recognition capabilities, nucleic acid-based self-assemblies represent a diverse toolbox for use by bioengineers to create molecules with potentially revolutionary biological activities. In this review, we focus on the development of self-assembling nucleic acid nanostructures that are functionalized with nucleic acid aptamers and their great potential in wide ranging application areas.
引用
收藏
页码:13797 / 13868
页数:72
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