Integrating Ligands into Nucleic Acid Systems

被引:1
|
作者
Wang, Yang [1 ,3 ]
Liu, Yan [3 ]
Wang, Liang-Liang [3 ]
Zhang, Qiu-Long [2 ,3 ]
Xu, Liang [3 ]
机构
[1] Sch Biomed Engn, Sch Med, Guangdong Key Lab Biomed Measurements & Ultrasound, Natl Reg Key Technol Engn Lab Med Ultrasound, Shenzhen 518060, Peoples R China
[2] Putian Univ, Sch Pharm & Med Technol, Putian 351100, Fujian, Peoples R China
[3] Sun Yat Sen Univ, Synthet Chem Sch Chem, MOE Key Lab Bioinorgan, Guangzhou 510275, Peoples R China
基金
中国国家自然科学基金;
关键词
Ligand Integration; Nucleic Acid Nanomachines; Biosensors; Gene Regulation; DNA STRAND DISPLACEMENT; GENE-EXPRESSION; SMALL MOLECULES; APTAMER; RNA; AMPLIFICATION; TOEHOLD; COMPUTATION; PRINCIPLES; APTAZYME;
D O I
10.1002/cbic.202300292
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Signal transduction from non-nucleic acid ligands (small molecules and proteins) to structural changes of nucleic acids plays a crucial role in both biomedical analysis and cellular regulations. However, how to bridge between these two types of molecules without compromising the expandable complexity and programmability of the nucleic acid nanomachines is a critical challenge. Compared with the previously most widely applied transduction strategies, we review the latest advances of a kinetically controlled approach for ligand-oligonucleotide transduction in this Concept article. This new design works through an intrinsic conformational alteration of the nucleic acid aptamer upon the ligand binding as a governing factor for nucleic acid strand displacement reactions. The functionalities and applications of this transduction system as a ligand converter on biosensing and DNA computation are described and discussed. Furthermore, we propose some potential scenarios for utilization of this ligand transduction design to regulate gene expression through synthetic RNA switches in the cellular contexts. Finally, future perspectives regarding this ligand-oligonucleotide transduction platform are also discussed.
引用
收藏
页数:6
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