Targeting nucleic acids using dynamic combinatorial chemistry

Date

2011

Authors

Durai, Chandramathi R. Sherman
Harding, Margaret

Journal Title

Journal ISSN

Volume Title

Publisher

CSIRO Publishing

Abstract

Dynamic combinatorial chemistry (DCC) is a powerful method for the identification of novel ligands for the molecular recognition of receptor molecules. The method relies on self-assembly processes to generate libraries of compounds under reversible conditions, allowing a receptor molecule to select the optimal binding ligand from the mixture. However, while DCC is now an established field of chemistry, there are limited examples of the application of DCC to nucleic acids. The requirement to conduct experiments under physiologically relevant conditions, and avoid reaction with, or denaturation of, the target nucleic acid secondary structure, limits the choice of the reversible chemistry, and presents restrictions on the building block design. This review will summarize recent examples of applications of DCC to the recognition of nucleic acids. Studies with duplex DNA, quadruplex DNA, and RNA have utilized mainly thiol disulfide libraries, although applications of imine libraries, in combination with metal coordination, have been reported. The use of thiol disulfide libraries produces lead compounds with limited biostability, and hence design of stable analogues or mimics is required for many applications.

Description

Keywords

Keywords: Biostability; Building blockes; Duplex DNA; Dynamic combinatorial chemistry; Metal coordination; Novel ligands; Optimal binding; Secondary structures; Self assembly process; Thiol-disulfide; Bioassay; Biochips; Lead compounds; Libraries; Ligands; Molecula

Citation

Source

Australian Journal of Chemistry

Type

Journal article

Book Title

Entity type

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Restricted until

2037-12-31