4.6 Review

G-Quadruplex-Forming Aptamers-Characteristics, Applications, and Perspectives

Journal

MOLECULES
Volume 24, Issue 20, Pages -

Publisher

MDPI
DOI: 10.3390/molecules24203781

Keywords

aptamers; G-quadruplexes; cancer; anticoagulants; aptasensors; antiviral agents; therapeutics; diagnostics; conjugates

Funding

  1. National Science Center grant [UMO-2017/25/B/NZ7/00127]

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G-quadruplexes constitute a unique class of nucleic acid structures formed by G-rich oligonucleotides of DNA- or RNA-type. Depending on their chemical nature, loops length, and localization in the sequence or structure molecularity, G-quadruplexes are highly polymorphic structures showing various folding topologies. They may be formed in the human genome where they are believed to play a pivotal role in the regulation of multiple biological processes such as replication, transcription, and translation. Thus, natural G-quadruplex structures became prospective targets for disease treatment. The fast development of systematic evolution of ligands by exponential enrichment (SELEX) technologies provided a number of G-rich aptamers revealing the potential of G-quadruplex structures as a promising molecular tool targeted toward various biologically important ligands. Because of their high stability, increased cellular uptake, ease of chemical modification, minor production costs, and convenient storage, G-rich aptamers became interesting therapeutic and diagnostic alternatives to antibodies. In this review, we describe the recent advances in the development of G-quadruplex based aptamers by focusing on the therapeutic and diagnostic potential of this exceptional class of nucleic acid structures.

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