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Acrylamide-dT: a polymerisable nucleoside for DNA incorporation

The synthesis of a novel modified nucleoside phosphoramidite, Acrylamide-dT-CE phosphoramidite, obtained in three steps from commercially available starting materials, is reported. It was readily incorporated into thrombin binding aptamer (TBA) sequences using automated solid-phase synthesis under u...

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Detalles Bibliográficos
Autores principales: Allabush, Francia, Mendes, Paula M., Tucker, James H. R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072585/
https://www.ncbi.nlm.nih.gov/pubmed/35527933
http://dx.doi.org/10.1039/c9ra07570d
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author Allabush, Francia
Mendes, Paula M.
Tucker, James H. R.
author_facet Allabush, Francia
Mendes, Paula M.
Tucker, James H. R.
author_sort Allabush, Francia
collection PubMed
description The synthesis of a novel modified nucleoside phosphoramidite, Acrylamide-dT-CE phosphoramidite, obtained in three steps from commercially available starting materials, is reported. It was readily incorporated into thrombin binding aptamer (TBA) sequences using automated solid-phase synthesis under ultra-mild conditions, with the modification shown not to adversely affect duplex stability, G-quadruplex structure, or thrombin binding. The reaction and integration of the modified strands with acrylamide polymers was evidenced by gel electrophoresis. The Acrylamide-dT functional handle promises to be an ideal synthon for preparing DNA–polymer hybrids for use in various macromolecular materials applications.
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spelling pubmed-90725852022-05-06 Acrylamide-dT: a polymerisable nucleoside for DNA incorporation Allabush, Francia Mendes, Paula M. Tucker, James H. R. RSC Adv Chemistry The synthesis of a novel modified nucleoside phosphoramidite, Acrylamide-dT-CE phosphoramidite, obtained in three steps from commercially available starting materials, is reported. It was readily incorporated into thrombin binding aptamer (TBA) sequences using automated solid-phase synthesis under ultra-mild conditions, with the modification shown not to adversely affect duplex stability, G-quadruplex structure, or thrombin binding. The reaction and integration of the modified strands with acrylamide polymers was evidenced by gel electrophoresis. The Acrylamide-dT functional handle promises to be an ideal synthon for preparing DNA–polymer hybrids for use in various macromolecular materials applications. The Royal Society of Chemistry 2019-10-03 /pmc/articles/PMC9072585/ /pubmed/35527933 http://dx.doi.org/10.1039/c9ra07570d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Allabush, Francia
Mendes, Paula M.
Tucker, James H. R.
Acrylamide-dT: a polymerisable nucleoside for DNA incorporation
title Acrylamide-dT: a polymerisable nucleoside for DNA incorporation
title_full Acrylamide-dT: a polymerisable nucleoside for DNA incorporation
title_fullStr Acrylamide-dT: a polymerisable nucleoside for DNA incorporation
title_full_unstemmed Acrylamide-dT: a polymerisable nucleoside for DNA incorporation
title_short Acrylamide-dT: a polymerisable nucleoside for DNA incorporation
title_sort acrylamide-dt: a polymerisable nucleoside for dna incorporation
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072585/
https://www.ncbi.nlm.nih.gov/pubmed/35527933
http://dx.doi.org/10.1039/c9ra07570d
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