Enhanced Stability of DNA Oligonucleotides with Partially Zwitterionic Backbone Structures in Biological Media

Deficient stability towards nuclease-mediated degradation is one of the most relevant tasks in the development of oligonucleotide-derived biomedical agents. This hurdle can be overcome through modifications to the native oligonucleotide backbone structure, with the goal of simultaneously retaining t...

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Main Authors: Melissa Meng, Boris Schmidtgall, Christian Ducho
Format: Article
Language:English
Published: MDPI AG 2018-11-01
Series:Molecules
Subjects:
DNA
Online Access:https://www.mdpi.com/1420-3049/23/11/2941
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spelling doaj-78ecaa1c6e084dd4b5d68101b8b53dfc2020-11-24T20:59:13ZengMDPI AGMolecules1420-30492018-11-012311294110.3390/molecules23112941molecules23112941Enhanced Stability of DNA Oligonucleotides with Partially Zwitterionic Backbone Structures in Biological MediaMelissa Meng0Boris Schmidtgall1Christian Ducho2Saarland University, Department of Pharmacy, Pharmaceutical and Medicinal Chemistry, Campus C2 3, 66123 Saarbrücken, GermanySaarland University, Department of Pharmacy, Pharmaceutical and Medicinal Chemistry, Campus C2 3, 66123 Saarbrücken, GermanySaarland University, Department of Pharmacy, Pharmaceutical and Medicinal Chemistry, Campus C2 3, 66123 Saarbrücken, GermanyDeficient stability towards nuclease-mediated degradation is one of the most relevant tasks in the development of oligonucleotide-derived biomedical agents. This hurdle can be overcome through modifications to the native oligonucleotide backbone structure, with the goal of simultaneously retaining the unique hybridization properties of nucleic acids. The nucleosyl amino acid (NAA)-modification is a recently introduced artificial cationic backbone linkage. Partially zwitterionic NAA-modified oligonucleotides had previously shown hybridization with DNA strands with retained base-pairing fidelity. In this study, we report the significantly enhanced stability of NAA-modified oligonucleotides towards 3′- and 5′-exonuclease-mediated degradation as well as in complex biological media such as human plasma and whole cell lysate. This demonstrates the potential versatility of the NAA-motif as a backbone modification for the development of biomedically active oligonucleotide analogues.https://www.mdpi.com/1420-3049/23/11/2941DNAoligonucleotidesbackbone modificationsnucleasesbiological media
collection DOAJ
language English
format Article
sources DOAJ
author Melissa Meng
Boris Schmidtgall
Christian Ducho
spellingShingle Melissa Meng
Boris Schmidtgall
Christian Ducho
Enhanced Stability of DNA Oligonucleotides with Partially Zwitterionic Backbone Structures in Biological Media
Molecules
DNA
oligonucleotides
backbone modifications
nucleases
biological media
author_facet Melissa Meng
Boris Schmidtgall
Christian Ducho
author_sort Melissa Meng
title Enhanced Stability of DNA Oligonucleotides with Partially Zwitterionic Backbone Structures in Biological Media
title_short Enhanced Stability of DNA Oligonucleotides with Partially Zwitterionic Backbone Structures in Biological Media
title_full Enhanced Stability of DNA Oligonucleotides with Partially Zwitterionic Backbone Structures in Biological Media
title_fullStr Enhanced Stability of DNA Oligonucleotides with Partially Zwitterionic Backbone Structures in Biological Media
title_full_unstemmed Enhanced Stability of DNA Oligonucleotides with Partially Zwitterionic Backbone Structures in Biological Media
title_sort enhanced stability of dna oligonucleotides with partially zwitterionic backbone structures in biological media
publisher MDPI AG
series Molecules
issn 1420-3049
publishDate 2018-11-01
description Deficient stability towards nuclease-mediated degradation is one of the most relevant tasks in the development of oligonucleotide-derived biomedical agents. This hurdle can be overcome through modifications to the native oligonucleotide backbone structure, with the goal of simultaneously retaining the unique hybridization properties of nucleic acids. The nucleosyl amino acid (NAA)-modification is a recently introduced artificial cationic backbone linkage. Partially zwitterionic NAA-modified oligonucleotides had previously shown hybridization with DNA strands with retained base-pairing fidelity. In this study, we report the significantly enhanced stability of NAA-modified oligonucleotides towards 3′- and 5′-exonuclease-mediated degradation as well as in complex biological media such as human plasma and whole cell lysate. This demonstrates the potential versatility of the NAA-motif as a backbone modification for the development of biomedically active oligonucleotide analogues.
topic DNA
oligonucleotides
backbone modifications
nucleases
biological media
url https://www.mdpi.com/1420-3049/23/11/2941
work_keys_str_mv AT melissameng enhancedstabilityofdnaoligonucleotideswithpartiallyzwitterionicbackbonestructuresinbiologicalmedia
AT borisschmidtgall enhancedstabilityofdnaoligonucleotideswithpartiallyzwitterionicbackbonestructuresinbiologicalmedia
AT christianducho enhancedstabilityofdnaoligonucleotideswithpartiallyzwitterionicbackbonestructuresinbiologicalmedia
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