Small-Molecule Binding Aptamers: Selection Strategies, Characterization, and Applications

被引:282
作者
Ruscito, Annemaria [1 ]
DeRosa, Maria C. [1 ]
机构
[1] Carleton Univ, Dept Chem, Ottawa, ON K1S 5B6, Canada
关键词
aptamer; small molecule; SELEX; in vitro selection; biosensor; IN-VITRO SELECTION; SURFACE-PLASMON RESONANCE; DNA-APTAMERS; LABEL-FREE; EXPONENTIAL ENRICHMENT; SYSTEMATIC EVOLUTION; RECOGNITION ELEMENT; OKADAIC ACID; SELEX; IDENTIFICATION;
D O I
10.3389/fchem.2016.00014
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Aptamers are single-stranded, synthetic oligonucleotides that fold into 3-dimensional shapes capable of binding non-covalently with high affinity and specificity to a target molecule. They are generated via an in vitro process known as the Systematic Evolution of Ligands by EXponential enrichment, from which candidates are screened and characterized, and then used in various applications. These applications range from therapeutic uses to biosensors for target detection. Aptamers for small molecule targets such as toxins, antibiotics, molecular markers, drugs, and heavy metals will be the focus of this review. Their accurate detection is needed for the protection and wellbeing of humans and animals. However, the small molecular weights of these targets, including the drastic size difference between the target and the oligonucleotides, make it challenging to select, characterize, and apply aptamers for their detection. Thus, recent (since 2012) notable advances in small molecule aptamers, which have overcome some of these challenges, are presented here, while defining challenges that still exist are discussed.
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页数:14
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