Automated Solid-Phase Click Synthesis of Oligonucleotide Conjugates: From Small Molecules to Diverse N‑Acetylgalactosamine Clusters

We developed a novel technique for the efficient conjugation of oligonucleotides with various alkyl azides such as fluorescent dyes, biotin, cholesterol, N-acetylgalactosamine (GalNAc), etc. using copper-catalysed alkyne–azide cycloaddition on the solid phase and CuI·P­(OEt)3 as a catalyst. Conjugat...

Full description

Saved in:
Bibliographic Details
Published inBioconjugate chemistry Vol. 28; no. 10; pp. 2599 - 2607
Main Authors Farzan, Valentina M, Ulashchik, Egor A, Martynenko-Makaev, Yury V, Kvach, Maksim V, Aparin, Ilya O, Brylev, Vladimir A, Prikazchikova, Tatiana A, Maklakova, Svetlana Yu, Majouga, Alexander G, Ustinov, Alexey V, Shipulin, German A, Shmanai, Vadim V, Korshun, Vladimir A, Zatsepin, Timofei S
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 18.10.2017
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:We developed a novel technique for the efficient conjugation of oligonucleotides with various alkyl azides such as fluorescent dyes, biotin, cholesterol, N-acetylgalactosamine (GalNAc), etc. using copper-catalysed alkyne–azide cycloaddition on the solid phase and CuI·P­(OEt)3 as a catalyst. Conjugation is carried out in an oligonucleotide synthesizer in fully automated mode and is coupled to oligonucleotide synthesis and on-column deprotection. We also suggest a set of reagents for the construction of diverse conjugates. The sequential double-click procedure using a pentaerythritol-derived tetraazide followed by the addition of a GalNAc or Tris–GalNAc alkyne gives oligonucleotide–GalNAc dendrimer conjugates in good yields with minimal excess of sophisticated alkyne reagents. The approach is suitable for high-throughput synthesis of oligonucleotide conjugates ranging from fluorescent DNA probes to various multi-GalNAc derivatives of 2′-modified siRNA.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1043-1802
1520-4812
DOI:10.1021/acs.bioconjchem.7b00462