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Solid‐Phase‐Supported Chemoenzymatic Synthesis of a Light‐Activatable tRNA Derivative

Herein, we present a multi‐cycle chemoenzymatic synthesis of modified RNA with simplified solid‐phase handling to overcome size limitations of RNA synthesis. It combines the advantages of classical chemical solid‐phase synthesis and enzymatic synthesis using magnetic streptavidin beads and biotinyla...

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Detalles Bibliográficos
Autores principales: Blümler, Anja, Schwalbe, Harald, Heckel, Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9299214/
https://www.ncbi.nlm.nih.gov/pubmed/34738704
http://dx.doi.org/10.1002/anie.202111613
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author Blümler, Anja
Schwalbe, Harald
Heckel, Alexander
author_facet Blümler, Anja
Schwalbe, Harald
Heckel, Alexander
author_sort Blümler, Anja
collection PubMed
description Herein, we present a multi‐cycle chemoenzymatic synthesis of modified RNA with simplified solid‐phase handling to overcome size limitations of RNA synthesis. It combines the advantages of classical chemical solid‐phase synthesis and enzymatic synthesis using magnetic streptavidin beads and biotinylated RNA. Successful introduction of light‐controllable RNA nucleotides into the tRNA(Met) sequence was confirmed by gel electrophoresis and mass spectrometry. The methods tolerate modifications in the RNA phosphodiester backbone and allow introductions of photocaged and photoswitchable nucleotides as well as photocleavable strand breaks and fluorophores.
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spelling pubmed-92992142022-07-21 Solid‐Phase‐Supported Chemoenzymatic Synthesis of a Light‐Activatable tRNA Derivative Blümler, Anja Schwalbe, Harald Heckel, Alexander Angew Chem Int Ed Engl Communications Herein, we present a multi‐cycle chemoenzymatic synthesis of modified RNA with simplified solid‐phase handling to overcome size limitations of RNA synthesis. It combines the advantages of classical chemical solid‐phase synthesis and enzymatic synthesis using magnetic streptavidin beads and biotinylated RNA. Successful introduction of light‐controllable RNA nucleotides into the tRNA(Met) sequence was confirmed by gel electrophoresis and mass spectrometry. The methods tolerate modifications in the RNA phosphodiester backbone and allow introductions of photocaged and photoswitchable nucleotides as well as photocleavable strand breaks and fluorophores. John Wiley and Sons Inc. 2021-11-22 2022-01-03 /pmc/articles/PMC9299214/ /pubmed/34738704 http://dx.doi.org/10.1002/anie.202111613 Text en © 2021 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Communications
Blümler, Anja
Schwalbe, Harald
Heckel, Alexander
Solid‐Phase‐Supported Chemoenzymatic Synthesis of a Light‐Activatable tRNA Derivative
title Solid‐Phase‐Supported Chemoenzymatic Synthesis of a Light‐Activatable tRNA Derivative
title_full Solid‐Phase‐Supported Chemoenzymatic Synthesis of a Light‐Activatable tRNA Derivative
title_fullStr Solid‐Phase‐Supported Chemoenzymatic Synthesis of a Light‐Activatable tRNA Derivative
title_full_unstemmed Solid‐Phase‐Supported Chemoenzymatic Synthesis of a Light‐Activatable tRNA Derivative
title_short Solid‐Phase‐Supported Chemoenzymatic Synthesis of a Light‐Activatable tRNA Derivative
title_sort solid‐phase‐supported chemoenzymatic synthesis of a light‐activatable trna derivative
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9299214/
https://www.ncbi.nlm.nih.gov/pubmed/34738704
http://dx.doi.org/10.1002/anie.202111613
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