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We describe the development of a chemical process based on the CuAAC reaction (click chemistry) to ligate DNA strands and produce an unnatural triazole backbone linkage. The chemical reaction is templated by a complementary DNA splint which accelerates the reaction and provides the required specificity. The resultant 1,4-triazole linkage is read through by DNA and RNA polymerases and is biocompatible in bacterial and human cells. This work has implications for the synthesis of chemically modified genes and other large modified DNA and RNA constructs.

Original publication

DOI

10.1017/S0033583515000141

Type

Journal article

Journal

Q Rev Biophys

Publication Date

11/2015

Volume

48

Pages

429 - 436

Keywords

Biocompatibility, Click chemistry, triazole DNA, Bacteria, Biocompatible Materials, Biophysical Phenomena, Click Chemistry, DNA, DNA, Complementary, DNA-Directed DNA Polymerase, Esters, Humans, Hydrogen Bonding, RNA, Thermodynamics, Transcription, Genetic, Triazoles