Enhancing aptamer function and stability via in vitro selection using modified nucleic acids

被引:55
|
作者
Meek, Kirsten N.
Rangel, Alexandra E.
Heemstra, Jennifer M. [1 ]
机构
[1] Univ Utah, Dept Chem, 315 S 1400 E, Salt Lake City, UT 84112 USA
关键词
Aptamer; Nucleic acid; In vitro selection; Affinity reagent; Polymerase engineering; Templated synthesis; ENDOTHELIAL GROWTH-FACTOR; BASE-PAIR; GENETIC ALPHABET; DNA-POLYMERASE; EXPONENTIAL ENRICHMENT; VASCULAR-PERMEABILITY; SYSTEMATIC EVOLUTION; HYDROPHOBIC BASE; RECEPTOR-BINDING; RNA LIGANDS;
D O I
10.1016/j.ymeth.2016.03.008
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Nucleic acid aptamers have emerged as a promising alternative to antibodies for use as recognition elements in therapeutics, bioimaging, and analytical applications. A key benefit that aptamers possess relative to antibodies is their ability to be chemically synthesized. This advantage, coupled with the broad range of modified nucleotide building blocks that can be constructed using chemical synthesis, has enabled the discovery and development of modified aptamers having extraordinary affinity, specificity, and biostability. Early efforts to generate modified aptamers focused on selection of a native DNA or RNA aptamer, followed by post-selection trial-and-error testing of modifications. However, recent advances in polymerase engineering and templated nucleic acid synthesis have enabled the direct selection of aptamers having modified backbones and nucleobases. This review will discuss these technological advances and highlight the improvements in aptamer function that have been realized through in vitro selection of non -natural nucleic acids. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:29 / 36
页数:8
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