Cargando…

Convergent synthesis of phosphorodiamidate morpholino oligonucleotides (PMOs) by the H-phosphonate approach

Phosphorodiamidate morpholino oligonucleotides (PMOs) are a promising type of antisense oligonucleotides, but their challenging synthesis makes them difficult to access. This research presents an efficient synthetic approach for PMOs using the H-phosphonate approach. The use of phosphonium-type cond...

Descripción completa

Detalles Bibliográficos
Autores principales: Tsurusaki, Taiki, Sato, Kazuki, Imai, Hiroki, Hirai, Kunihiro, Takahashi, Daisuke, Wada, Takeshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10400599/
https://www.ncbi.nlm.nih.gov/pubmed/37537221
http://dx.doi.org/10.1038/s41598-023-38698-2
_version_ 1785084479261376512
author Tsurusaki, Taiki
Sato, Kazuki
Imai, Hiroki
Hirai, Kunihiro
Takahashi, Daisuke
Wada, Takeshi
author_facet Tsurusaki, Taiki
Sato, Kazuki
Imai, Hiroki
Hirai, Kunihiro
Takahashi, Daisuke
Wada, Takeshi
author_sort Tsurusaki, Taiki
collection PubMed
description Phosphorodiamidate morpholino oligonucleotides (PMOs) are a promising type of antisense oligonucleotides, but their challenging synthesis makes them difficult to access. This research presents an efficient synthetic approach for PMOs using the H-phosphonate approach. The use of phosphonium-type condensing reagents significantly reduced coupling times compared with the current synthetic approach. Furthermore, phosphonium-type condensing reagents facilitated the fragment condensation of PMO, synthesizing up to 8-mer containing all four nucleobases with remarkable coupling efficacy. This is the first report on the convergent synthesis of PMOs. This approach would facilitate the large-scale synthesis of PMOs and accelerate their popularity and accessibility as a next-generation therapy.
format Online
Article
Text
id pubmed-10400599
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-104005992023-08-05 Convergent synthesis of phosphorodiamidate morpholino oligonucleotides (PMOs) by the H-phosphonate approach Tsurusaki, Taiki Sato, Kazuki Imai, Hiroki Hirai, Kunihiro Takahashi, Daisuke Wada, Takeshi Sci Rep Article Phosphorodiamidate morpholino oligonucleotides (PMOs) are a promising type of antisense oligonucleotides, but their challenging synthesis makes them difficult to access. This research presents an efficient synthetic approach for PMOs using the H-phosphonate approach. The use of phosphonium-type condensing reagents significantly reduced coupling times compared with the current synthetic approach. Furthermore, phosphonium-type condensing reagents facilitated the fragment condensation of PMO, synthesizing up to 8-mer containing all four nucleobases with remarkable coupling efficacy. This is the first report on the convergent synthesis of PMOs. This approach would facilitate the large-scale synthesis of PMOs and accelerate their popularity and accessibility as a next-generation therapy. Nature Publishing Group UK 2023-08-03 /pmc/articles/PMC10400599/ /pubmed/37537221 http://dx.doi.org/10.1038/s41598-023-38698-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Tsurusaki, Taiki
Sato, Kazuki
Imai, Hiroki
Hirai, Kunihiro
Takahashi, Daisuke
Wada, Takeshi
Convergent synthesis of phosphorodiamidate morpholino oligonucleotides (PMOs) by the H-phosphonate approach
title Convergent synthesis of phosphorodiamidate morpholino oligonucleotides (PMOs) by the H-phosphonate approach
title_full Convergent synthesis of phosphorodiamidate morpholino oligonucleotides (PMOs) by the H-phosphonate approach
title_fullStr Convergent synthesis of phosphorodiamidate morpholino oligonucleotides (PMOs) by the H-phosphonate approach
title_full_unstemmed Convergent synthesis of phosphorodiamidate morpholino oligonucleotides (PMOs) by the H-phosphonate approach
title_short Convergent synthesis of phosphorodiamidate morpholino oligonucleotides (PMOs) by the H-phosphonate approach
title_sort convergent synthesis of phosphorodiamidate morpholino oligonucleotides (pmos) by the h-phosphonate approach
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10400599/
https://www.ncbi.nlm.nih.gov/pubmed/37537221
http://dx.doi.org/10.1038/s41598-023-38698-2
work_keys_str_mv AT tsurusakitaiki convergentsynthesisofphosphorodiamidatemorpholinooligonucleotidespmosbythehphosphonateapproach
AT satokazuki convergentsynthesisofphosphorodiamidatemorpholinooligonucleotidespmosbythehphosphonateapproach
AT imaihiroki convergentsynthesisofphosphorodiamidatemorpholinooligonucleotidespmosbythehphosphonateapproach
AT hiraikunihiro convergentsynthesisofphosphorodiamidatemorpholinooligonucleotidespmosbythehphosphonateapproach
AT takahashidaisuke convergentsynthesisofphosphorodiamidatemorpholinooligonucleotidespmosbythehphosphonateapproach
AT wadatakeshi convergentsynthesisofphosphorodiamidatemorpholinooligonucleotidespmosbythehphosphonateapproach