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Investigation of factors influencing the separation of diastereomers of phosphorothioated oligonucleotides
This study presents a systematic investigation of factors influencing the chromatographic separation of diastereomers of phosphorothioated pentameric oligonucleotides as model solutes. Separation was carried out under ion-pairing conditions using an XBridge C(18) column. For oligonucleotides with a...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6543027/ https://www.ncbi.nlm.nih.gov/pubmed/31020370 http://dx.doi.org/10.1007/s00216-019-01813-2 |
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author | Enmark, Martin Rova, Maria Samuelsson, Jörgen Örnskov, Eivor Schweikart, Fritz Fornstedt, Torgny |
author_facet | Enmark, Martin Rova, Maria Samuelsson, Jörgen Örnskov, Eivor Schweikart, Fritz Fornstedt, Torgny |
author_sort | Enmark, Martin |
collection | PubMed |
description | This study presents a systematic investigation of factors influencing the chromatographic separation of diastereomers of phosphorothioated pentameric oligonucleotides as model solutes. Separation was carried out under ion-pairing conditions using an XBridge C(18) column. For oligonucleotides with a single sulfur substitution, the diastereomer selectivity was found to increase with decreasing carbon chain length of the tertiary alkylamine used as an ion-pair reagent. Using an ion-pair reagent with high selectivity for diastereomers, triethylammonium, it was found the selectivity increased with decreased ion-pair concentration and shallower gradient slope. Selectivity was also demonstrated to be dependent on the position of the modified linkage. Substitutions at the center of the pentamer resulted in higher diastereomer selectivity compared to substitutions at either end. For mono-substituted oligonucleotides, the retention order and stereo configuration were consistently found to be correlated, with Rp followed by Sp, regardless of which linkage was modified. The type of nucleobase greatly affects the observed selectivity. A pentamer of cytosine has about twice the diastereomer selectivity of that of thymine. When investigating the retention of various oligonucleotides eluted using tributylammonium as the ion-pairing reagent, no diastereomer selectivity could be observed. However, retention was found to be dependent on both the degree and position of sulfur substitution as well as on the nucleobase. When analyzing fractions collected in the front and tail of overloaded injections, a significant difference was found in the ratio between Rp and Sp diastereomers, indicating that the peak broadening observed when using tributylammonium could be explained by partial diastereomer separation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00216-019-01813-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6543027 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-65430272019-06-19 Investigation of factors influencing the separation of diastereomers of phosphorothioated oligonucleotides Enmark, Martin Rova, Maria Samuelsson, Jörgen Örnskov, Eivor Schweikart, Fritz Fornstedt, Torgny Anal Bioanal Chem Research Paper This study presents a systematic investigation of factors influencing the chromatographic separation of diastereomers of phosphorothioated pentameric oligonucleotides as model solutes. Separation was carried out under ion-pairing conditions using an XBridge C(18) column. For oligonucleotides with a single sulfur substitution, the diastereomer selectivity was found to increase with decreasing carbon chain length of the tertiary alkylamine used as an ion-pair reagent. Using an ion-pair reagent with high selectivity for diastereomers, triethylammonium, it was found the selectivity increased with decreased ion-pair concentration and shallower gradient slope. Selectivity was also demonstrated to be dependent on the position of the modified linkage. Substitutions at the center of the pentamer resulted in higher diastereomer selectivity compared to substitutions at either end. For mono-substituted oligonucleotides, the retention order and stereo configuration were consistently found to be correlated, with Rp followed by Sp, regardless of which linkage was modified. The type of nucleobase greatly affects the observed selectivity. A pentamer of cytosine has about twice the diastereomer selectivity of that of thymine. When investigating the retention of various oligonucleotides eluted using tributylammonium as the ion-pairing reagent, no diastereomer selectivity could be observed. However, retention was found to be dependent on both the degree and position of sulfur substitution as well as on the nucleobase. When analyzing fractions collected in the front and tail of overloaded injections, a significant difference was found in the ratio between Rp and Sp diastereomers, indicating that the peak broadening observed when using tributylammonium could be explained by partial diastereomer separation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00216-019-01813-2) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2019-04-24 2019 /pmc/articles/PMC6543027/ /pubmed/31020370 http://dx.doi.org/10.1007/s00216-019-01813-2 Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Research Paper Enmark, Martin Rova, Maria Samuelsson, Jörgen Örnskov, Eivor Schweikart, Fritz Fornstedt, Torgny Investigation of factors influencing the separation of diastereomers of phosphorothioated oligonucleotides |
title | Investigation of factors influencing the separation of diastereomers of phosphorothioated oligonucleotides |
title_full | Investigation of factors influencing the separation of diastereomers of phosphorothioated oligonucleotides |
title_fullStr | Investigation of factors influencing the separation of diastereomers of phosphorothioated oligonucleotides |
title_full_unstemmed | Investigation of factors influencing the separation of diastereomers of phosphorothioated oligonucleotides |
title_short | Investigation of factors influencing the separation of diastereomers of phosphorothioated oligonucleotides |
title_sort | investigation of factors influencing the separation of diastereomers of phosphorothioated oligonucleotides |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6543027/ https://www.ncbi.nlm.nih.gov/pubmed/31020370 http://dx.doi.org/10.1007/s00216-019-01813-2 |
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