4.7 Article

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

Journal

METHODS
Volume 106, Issue -, Pages 29-36

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ymeth.2016.03.008

Keywords

Aptamer; Nucleic acid; In vitro selection; Affinity reagent; Polymerase engineering; Templated synthesis

Funding

  1. DARPA Folded Non-Natural Polymers with Biological Function (Fold F(x)) Program [N66001-14-2-4054]

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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.

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