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Synthesis and evaluation of modified siRNA molecules containing a novel glucose derivative

Chemical modifications are critical for the development of safe and effective siRNAs for downstream applications. In this study, we report the synthesis of a novel glucose phosphoramidite, a triazole-linked to uracil at position one, for incorporation into oligonucleotides. Biological testing reveal...

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Detalles Bibliográficos
Autores principales: Salim, Lidya, Goss, Eva, Desaulniers, Jean-Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8698894/
https://www.ncbi.nlm.nih.gov/pubmed/35423452
http://dx.doi.org/10.1039/d1ra00922b
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author Salim, Lidya
Goss, Eva
Desaulniers, Jean-Paul
author_facet Salim, Lidya
Goss, Eva
Desaulniers, Jean-Paul
author_sort Salim, Lidya
collection PubMed
description Chemical modifications are critical for the development of safe and effective siRNAs for downstream applications. In this study, we report the synthesis of a novel glucose phosphoramidite, a triazole-linked to uracil at position one, for incorporation into oligonucleotides. Biological testing revealed that the glucose derivative at key positions within the sense or antisense strand can lead to potent gene-silencing activity, thus highlighting its tolerance in both sense and antisense positions. Furthermore, the A-form helical formation was maintained with this modification. Overall, placing the modification at the 3′ end and at key internal positions led to effective RNAi gene-silencing activity.
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spelling pubmed-86988942022-04-13 Synthesis and evaluation of modified siRNA molecules containing a novel glucose derivative Salim, Lidya Goss, Eva Desaulniers, Jean-Paul RSC Adv Chemistry Chemical modifications are critical for the development of safe and effective siRNAs for downstream applications. In this study, we report the synthesis of a novel glucose phosphoramidite, a triazole-linked to uracil at position one, for incorporation into oligonucleotides. Biological testing revealed that the glucose derivative at key positions within the sense or antisense strand can lead to potent gene-silencing activity, thus highlighting its tolerance in both sense and antisense positions. Furthermore, the A-form helical formation was maintained with this modification. Overall, placing the modification at the 3′ end and at key internal positions led to effective RNAi gene-silencing activity. The Royal Society of Chemistry 2021-03-01 /pmc/articles/PMC8698894/ /pubmed/35423452 http://dx.doi.org/10.1039/d1ra00922b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Salim, Lidya
Goss, Eva
Desaulniers, Jean-Paul
Synthesis and evaluation of modified siRNA molecules containing a novel glucose derivative
title Synthesis and evaluation of modified siRNA molecules containing a novel glucose derivative
title_full Synthesis and evaluation of modified siRNA molecules containing a novel glucose derivative
title_fullStr Synthesis and evaluation of modified siRNA molecules containing a novel glucose derivative
title_full_unstemmed Synthesis and evaluation of modified siRNA molecules containing a novel glucose derivative
title_short Synthesis and evaluation of modified siRNA molecules containing a novel glucose derivative
title_sort synthesis and evaluation of modified sirna molecules containing a novel glucose derivative
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8698894/
https://www.ncbi.nlm.nih.gov/pubmed/35423452
http://dx.doi.org/10.1039/d1ra00922b
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