Automated solid phase click synthesis of oligonucleotide conjugates: from small molecules to diverse N-acetylgalactosamine clusters

Farzan, V.M.; Ulashchik, E.A.; Martynenko-Makaev, Y.V.; Kvach, M.V.; Aparin, I.O.; Brylev, V.A.; Prikazchikova, T.A.; Maklakova, S.Y.; Majouga, A.G.; Ustinov, A.V.; Shipulin, G.A.; Shmanai, V.V.; Korshun, V.A.; Zatsepin, T.S.

Авторы: Farzan Valentina M., Ulashchik Egor A., Martynenko-Makaev Yury V., Kvach Maksim V., Aparin Ilya Olegovich, 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.
Журнал: Bioconjugate Chemistry
Год издания: 2017
Издательство: American Chemical Society
Местоположение издательства: United States
DOI: 10.1021/acs.bioconjchem.7b00462
Аннотация: We developed a novel technique for efficient conjugation of oligonucleotides with various alkyl azides (fluorescent dyes, biotin, cholesterol, GalNAc, etc.) using CuAAC on 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.
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Интеллектуальная Система Тематического Исследования НАукометрических данных

Automated solid phase click synthesis of oligonucleotide conjugates: from small molecules to diverse N-acetylgalactosamine clustersстатья