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Synthesis and optical properties of pyrrolidinyl peptide nucleic acid carrying a clicked Nile red label

DNA or its analogues with an environment-sensitive fluorescent label are potentially useful as a probe for studying the structure and dynamics of nucleic acids. In this work, pyrrolidinyl peptide nucleic acid (acpcPNA) was labeled at its backbone with Nile red, a solvatochromic benzophenoxazine dye,...

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Autores principales: Yotapan, Nattawut, Charoenpakdee, Chayan, Wathanathavorn, Pawinee, Ditmangklo, Boonsong, Wagenknecht, Hans-Achim, Vilaivan, Tirayut
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4168962/
https://www.ncbi.nlm.nih.gov/pubmed/25246975
http://dx.doi.org/10.3762/bjoc.10.224
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author Yotapan, Nattawut
Charoenpakdee, Chayan
Wathanathavorn, Pawinee
Ditmangklo, Boonsong
Wagenknecht, Hans-Achim
Vilaivan, Tirayut
author_facet Yotapan, Nattawut
Charoenpakdee, Chayan
Wathanathavorn, Pawinee
Ditmangklo, Boonsong
Wagenknecht, Hans-Achim
Vilaivan, Tirayut
author_sort Yotapan, Nattawut
collection PubMed
description DNA or its analogues with an environment-sensitive fluorescent label are potentially useful as a probe for studying the structure and dynamics of nucleic acids. In this work, pyrrolidinyl peptide nucleic acid (acpcPNA) was labeled at its backbone with Nile red, a solvatochromic benzophenoxazine dye, by means of click chemistry. The optical properties of the Nile red-labeled acpcPNA were investigated by UV–vis and fluorescence spectroscopy in the absence and in the presence of DNA. In contrast to the usual quenching observed in Nile red-labeled DNA, the hybridization with DNA resulted in blue shifting and an enhanced fluorescence regardless of the neighboring bases. More pronounced blue shifts and fluorescence enhancements were observed when the DNA target carried a base insertion in close proximity to the Nile red label. The results indicate that the Nile red label is located in a more hydrophobic environment in acpcPNA–DNA duplexes than in the single-stranded acpcPNA. The different fluorescence properties of the acpcPNA hybrids of complementary DNA and DNA carrying a base insertion are suggestive of different interactions between the Nile red label and the duplexes.
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spelling pubmed-41689622014-09-22 Synthesis and optical properties of pyrrolidinyl peptide nucleic acid carrying a clicked Nile red label Yotapan, Nattawut Charoenpakdee, Chayan Wathanathavorn, Pawinee Ditmangklo, Boonsong Wagenknecht, Hans-Achim Vilaivan, Tirayut Beilstein J Org Chem Full Research Paper DNA or its analogues with an environment-sensitive fluorescent label are potentially useful as a probe for studying the structure and dynamics of nucleic acids. In this work, pyrrolidinyl peptide nucleic acid (acpcPNA) was labeled at its backbone with Nile red, a solvatochromic benzophenoxazine dye, by means of click chemistry. The optical properties of the Nile red-labeled acpcPNA were investigated by UV–vis and fluorescence spectroscopy in the absence and in the presence of DNA. In contrast to the usual quenching observed in Nile red-labeled DNA, the hybridization with DNA resulted in blue shifting and an enhanced fluorescence regardless of the neighboring bases. More pronounced blue shifts and fluorescence enhancements were observed when the DNA target carried a base insertion in close proximity to the Nile red label. The results indicate that the Nile red label is located in a more hydrophobic environment in acpcPNA–DNA duplexes than in the single-stranded acpcPNA. The different fluorescence properties of the acpcPNA hybrids of complementary DNA and DNA carrying a base insertion are suggestive of different interactions between the Nile red label and the duplexes. Beilstein-Institut 2014-09-11 /pmc/articles/PMC4168962/ /pubmed/25246975 http://dx.doi.org/10.3762/bjoc.10.224 Text en Copyright © 2014, Yotapan et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Yotapan, Nattawut
Charoenpakdee, Chayan
Wathanathavorn, Pawinee
Ditmangklo, Boonsong
Wagenknecht, Hans-Achim
Vilaivan, Tirayut
Synthesis and optical properties of pyrrolidinyl peptide nucleic acid carrying a clicked Nile red label
title Synthesis and optical properties of pyrrolidinyl peptide nucleic acid carrying a clicked Nile red label
title_full Synthesis and optical properties of pyrrolidinyl peptide nucleic acid carrying a clicked Nile red label
title_fullStr Synthesis and optical properties of pyrrolidinyl peptide nucleic acid carrying a clicked Nile red label
title_full_unstemmed Synthesis and optical properties of pyrrolidinyl peptide nucleic acid carrying a clicked Nile red label
title_short Synthesis and optical properties of pyrrolidinyl peptide nucleic acid carrying a clicked Nile red label
title_sort synthesis and optical properties of pyrrolidinyl peptide nucleic acid carrying a clicked nile red label
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4168962/
https://www.ncbi.nlm.nih.gov/pubmed/25246975
http://dx.doi.org/10.3762/bjoc.10.224
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