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Polyanionic Carboxyethyl Peptide Nucleic Acids (ce-PNAs): Synthesis and DNA Binding
New polyanionic modifications of polyamide nucleic acid mimics were obtained. Thymine decamers were synthesized from respective chiral α- and γ-monomers, and their enantiomeric purity was assessed. Here, we present the decamer synthesis, purification and characterization by MALDI-TOF mass spectromet...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4607454/ https://www.ncbi.nlm.nih.gov/pubmed/26469337 http://dx.doi.org/10.1371/journal.pone.0140468 |
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author | Kirillova, Yuliya Boyarskaya, Nataliya Dezhenkov, Andrey Tankevich, Mariya Prokhorov, Ivan Varizhuk, Anna Eremin, Sergei Esipov, Dmitry Smirnov, Igor Pozmogova, Galina |
author_facet | Kirillova, Yuliya Boyarskaya, Nataliya Dezhenkov, Andrey Tankevich, Mariya Prokhorov, Ivan Varizhuk, Anna Eremin, Sergei Esipov, Dmitry Smirnov, Igor Pozmogova, Galina |
author_sort | Kirillova, Yuliya |
collection | PubMed |
description | New polyanionic modifications of polyamide nucleic acid mimics were obtained. Thymine decamers were synthesized from respective chiral α- and γ-monomers, and their enantiomeric purity was assessed. Here, we present the decamer synthesis, purification and characterization by MALDI-TOF mass spectrometry and an investigation of the hybridization properties of the decamers. We show that the modified γ-S-carboxyethyl-T(10) PNA forms a stable triplex with polyadenine DNA. |
format | Online Article Text |
id | pubmed-4607454 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-46074542015-10-29 Polyanionic Carboxyethyl Peptide Nucleic Acids (ce-PNAs): Synthesis and DNA Binding Kirillova, Yuliya Boyarskaya, Nataliya Dezhenkov, Andrey Tankevich, Mariya Prokhorov, Ivan Varizhuk, Anna Eremin, Sergei Esipov, Dmitry Smirnov, Igor Pozmogova, Galina PLoS One Research Article New polyanionic modifications of polyamide nucleic acid mimics were obtained. Thymine decamers were synthesized from respective chiral α- and γ-monomers, and their enantiomeric purity was assessed. Here, we present the decamer synthesis, purification and characterization by MALDI-TOF mass spectrometry and an investigation of the hybridization properties of the decamers. We show that the modified γ-S-carboxyethyl-T(10) PNA forms a stable triplex with polyadenine DNA. Public Library of Science 2015-10-15 /pmc/articles/PMC4607454/ /pubmed/26469337 http://dx.doi.org/10.1371/journal.pone.0140468 Text en © 2015 Kirillova et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Kirillova, Yuliya Boyarskaya, Nataliya Dezhenkov, Andrey Tankevich, Mariya Prokhorov, Ivan Varizhuk, Anna Eremin, Sergei Esipov, Dmitry Smirnov, Igor Pozmogova, Galina Polyanionic Carboxyethyl Peptide Nucleic Acids (ce-PNAs): Synthesis and DNA Binding |
title | Polyanionic Carboxyethyl Peptide Nucleic Acids (ce-PNAs): Synthesis and DNA Binding |
title_full | Polyanionic Carboxyethyl Peptide Nucleic Acids (ce-PNAs): Synthesis and DNA Binding |
title_fullStr | Polyanionic Carboxyethyl Peptide Nucleic Acids (ce-PNAs): Synthesis and DNA Binding |
title_full_unstemmed | Polyanionic Carboxyethyl Peptide Nucleic Acids (ce-PNAs): Synthesis and DNA Binding |
title_short | Polyanionic Carboxyethyl Peptide Nucleic Acids (ce-PNAs): Synthesis and DNA Binding |
title_sort | polyanionic carboxyethyl peptide nucleic acids (ce-pnas): synthesis and dna binding |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4607454/ https://www.ncbi.nlm.nih.gov/pubmed/26469337 http://dx.doi.org/10.1371/journal.pone.0140468 |
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