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Site-specific biotinylation of RNA molecules by transcription using unnatural base pairs

Direct site-specific biotinylation of RNA molecules was achieved by specific transcription mediated by unnatural base pairs. Unnatural base pairs between 2-amino-6-(2-thienyl)purine (denoted by s) and 2-oxo(1H)pyridine (denoted by y), or 2-amino-6-(2-thiazolyl)purine (denoted as v) and y specificall...

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Autores principales: Moriyama, Kei, Kimoto, Michiko, Mitsui, Tsuneo, Yokoyama, Shigeyuki, Hirao, Ichiro
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1188086/
https://www.ncbi.nlm.nih.gov/pubmed/16113238
http://dx.doi.org/10.1093/nar/gni128
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author Moriyama, Kei
Kimoto, Michiko
Mitsui, Tsuneo
Yokoyama, Shigeyuki
Hirao, Ichiro
author_facet Moriyama, Kei
Kimoto, Michiko
Mitsui, Tsuneo
Yokoyama, Shigeyuki
Hirao, Ichiro
author_sort Moriyama, Kei
collection PubMed
description Direct site-specific biotinylation of RNA molecules was achieved by specific transcription mediated by unnatural base pairs. Unnatural base pairs between 2-amino-6-(2-thienyl)purine (denoted by s) and 2-oxo(1H)pyridine (denoted by y), or 2-amino-6-(2-thiazolyl)purine (denoted as v) and y specifically function in T7 transcription. Using these unnatural base pairs, the substrate of biotinylated-y (Bio-yTP) was selectively incorporated into RNA, opposite s or v in the DNA templates, by T7 RNA polymerase. This method was applied to the immobilization of an RNA aptamer on sensor chips, and the aptamer accurately recognized its target protein. This direct site-specific biotinylation will provide a tool for RNA-based biotechnologies.
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spelling pubmed-11880862005-08-22 Site-specific biotinylation of RNA molecules by transcription using unnatural base pairs Moriyama, Kei Kimoto, Michiko Mitsui, Tsuneo Yokoyama, Shigeyuki Hirao, Ichiro Nucleic Acids Res Methods Online Direct site-specific biotinylation of RNA molecules was achieved by specific transcription mediated by unnatural base pairs. Unnatural base pairs between 2-amino-6-(2-thienyl)purine (denoted by s) and 2-oxo(1H)pyridine (denoted by y), or 2-amino-6-(2-thiazolyl)purine (denoted as v) and y specifically function in T7 transcription. Using these unnatural base pairs, the substrate of biotinylated-y (Bio-yTP) was selectively incorporated into RNA, opposite s or v in the DNA templates, by T7 RNA polymerase. This method was applied to the immobilization of an RNA aptamer on sensor chips, and the aptamer accurately recognized its target protein. This direct site-specific biotinylation will provide a tool for RNA-based biotechnologies. Oxford University Press 2005 2005-08-19 /pmc/articles/PMC1188086/ /pubmed/16113238 http://dx.doi.org/10.1093/nar/gni128 Text en © The Author 2005. Published by Oxford University Press. All rights reserved
spellingShingle Methods Online
Moriyama, Kei
Kimoto, Michiko
Mitsui, Tsuneo
Yokoyama, Shigeyuki
Hirao, Ichiro
Site-specific biotinylation of RNA molecules by transcription using unnatural base pairs
title Site-specific biotinylation of RNA molecules by transcription using unnatural base pairs
title_full Site-specific biotinylation of RNA molecules by transcription using unnatural base pairs
title_fullStr Site-specific biotinylation of RNA molecules by transcription using unnatural base pairs
title_full_unstemmed Site-specific biotinylation of RNA molecules by transcription using unnatural base pairs
title_short Site-specific biotinylation of RNA molecules by transcription using unnatural base pairs
title_sort site-specific biotinylation of rna molecules by transcription using unnatural base pairs
topic Methods Online
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1188086/
https://www.ncbi.nlm.nih.gov/pubmed/16113238
http://dx.doi.org/10.1093/nar/gni128
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