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Nucleoside Sensing
A rigid molecular clip comprising bisphosphonate binding sites and aromatic sidewalls forming an electron-rich cavity is able to distinguish between nucleosides and nucleotides in aqueous solution. Neutral nucleosides as well as antibiotics derived thereof are drawn into the unpolar interior of the...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International (MDPI)
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3926528/ |
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author | Fokkens, Michael Klärner, Frank-Gerrit Schrader, Thomas |
author_facet | Fokkens, Michael Klärner, Frank-Gerrit Schrader, Thomas |
author_sort | Fokkens, Michael |
collection | PubMed |
description | A rigid molecular clip comprising bisphosphonate binding sites and aromatic sidewalls forming an electron-rich cavity is able to distinguish between nucleosides and nucleotides in aqueous solution. Neutral nucleosides as well as antibiotics derived thereof are drawn into the unpolar interior of the cleft and lead to substantial upfield-shifts in the (1)H NMR spectrum. Nucleoside drugs can therefore be detected with high selectivity in the presence of their phosphorylated pendants or nucleic acids. |
format | Online Article Text |
id | pubmed-3926528 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
spelling | pubmed-39265282014-02-18 Nucleoside Sensing Fokkens, Michael Klärner, Frank-Gerrit Schrader, Thomas Sensors (Basel) Full Research Paper A rigid molecular clip comprising bisphosphonate binding sites and aromatic sidewalls forming an electron-rich cavity is able to distinguish between nucleosides and nucleotides in aqueous solution. Neutral nucleosides as well as antibiotics derived thereof are drawn into the unpolar interior of the cleft and lead to substantial upfield-shifts in the (1)H NMR spectrum. Nucleoside drugs can therefore be detected with high selectivity in the presence of their phosphorylated pendants or nucleic acids. Molecular Diversity Preservation International (MDPI) 2006-08-24 /pmc/articles/PMC3926528/ Text en 2006 by MDPI (http://www.mdpi.org). Reproduction is permitted for noncommercial purposes. |
spellingShingle | Full Research Paper Fokkens, Michael Klärner, Frank-Gerrit Schrader, Thomas Nucleoside Sensing |
title | Nucleoside Sensing |
title_full | Nucleoside Sensing |
title_fullStr | Nucleoside Sensing |
title_full_unstemmed | Nucleoside Sensing |
title_short | Nucleoside Sensing |
title_sort | nucleoside sensing |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3926528/ |
work_keys_str_mv | AT fokkensmichael nucleosidesensing AT klarnerfrankgerrit nucleosidesensing AT schraderthomas nucleosidesensing |