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The synthesis of 2′-methylseleno adenosine and guanosine 5′-triphosphates

Modified nucleoside triphosphates (NTPs) represent powerful building blocks to generate nucleic acids with novel properties by enzymatic synthesis. We have recently demonstrated the access to 2′-SeCH(3)-uridine and 2′-SeCH(3)-cytidine derivatized RNAs for applications in RNA crystallography, using t...

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Detalles Bibliográficos
Autores principales: Santner, Tobias, Siegmund, Vanessa, Marx, Andreas, Micura, Ronald
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3334826/
https://www.ncbi.nlm.nih.gov/pubmed/22364745
http://dx.doi.org/10.1016/j.bmc.2012.01.044
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author Santner, Tobias
Siegmund, Vanessa
Marx, Andreas
Micura, Ronald
author_facet Santner, Tobias
Siegmund, Vanessa
Marx, Andreas
Micura, Ronald
author_sort Santner, Tobias
collection PubMed
description Modified nucleoside triphosphates (NTPs) represent powerful building blocks to generate nucleic acids with novel properties by enzymatic synthesis. We have recently demonstrated the access to 2′-SeCH(3)-uridine and 2′-SeCH(3)-cytidine derivatized RNAs for applications in RNA crystallography, using the corresponding nucleoside triphosphates and distinct mutants of T7 RNA polymerase. In the present note, we introduce the chemical synthesis of the novel 2′-methylseleno-2′-deoxyadenosine and -guanosine 5′-triphosphates (2′-SeCH(3)-ATP and 2′-SeCH(3)-GTP) that represent further candidates for the enzymatic RNA synthesis with engineered RNA polymerases.
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spelling pubmed-33348262012-04-26 The synthesis of 2′-methylseleno adenosine and guanosine 5′-triphosphates Santner, Tobias Siegmund, Vanessa Marx, Andreas Micura, Ronald Bioorg Med Chem Article Modified nucleoside triphosphates (NTPs) represent powerful building blocks to generate nucleic acids with novel properties by enzymatic synthesis. We have recently demonstrated the access to 2′-SeCH(3)-uridine and 2′-SeCH(3)-cytidine derivatized RNAs for applications in RNA crystallography, using the corresponding nucleoside triphosphates and distinct mutants of T7 RNA polymerase. In the present note, we introduce the chemical synthesis of the novel 2′-methylseleno-2′-deoxyadenosine and -guanosine 5′-triphosphates (2′-SeCH(3)-ATP and 2′-SeCH(3)-GTP) that represent further candidates for the enzymatic RNA synthesis with engineered RNA polymerases. Elsevier Science 2012-04-01 /pmc/articles/PMC3334826/ /pubmed/22364745 http://dx.doi.org/10.1016/j.bmc.2012.01.044 Text en © 2012 Elsevier Ltd. https://creativecommons.org/licenses/by-nc-nd/3.0/ Open Access under CC BY-NC-ND 3.0 (https://creativecommons.org/licenses/by-nc-nd/3.0/) license
spellingShingle Article
Santner, Tobias
Siegmund, Vanessa
Marx, Andreas
Micura, Ronald
The synthesis of 2′-methylseleno adenosine and guanosine 5′-triphosphates
title The synthesis of 2′-methylseleno adenosine and guanosine 5′-triphosphates
title_full The synthesis of 2′-methylseleno adenosine and guanosine 5′-triphosphates
title_fullStr The synthesis of 2′-methylseleno adenosine and guanosine 5′-triphosphates
title_full_unstemmed The synthesis of 2′-methylseleno adenosine and guanosine 5′-triphosphates
title_short The synthesis of 2′-methylseleno adenosine and guanosine 5′-triphosphates
title_sort synthesis of 2′-methylseleno adenosine and guanosine 5′-triphosphates
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3334826/
https://www.ncbi.nlm.nih.gov/pubmed/22364745
http://dx.doi.org/10.1016/j.bmc.2012.01.044
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