Increasing the activity of DNAzyme based on the telomeric sequence: 2’-OMe-RNA and LNA modifications

2’-OMe-RNA analogues and LNA point modifications of DNA oligonucleotides were applied for the modulation of the G-quadruplex topology and enhancement of peroxidase activity of the resulting DNAzymes. The effect of the 2’-OMe-RNA analogue was studied for full length modified oligonucleotides with var...

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Main Authors: Kosman J., Żukowski K., Juskowiak B.
Format: Article
Language:English
Published: De Gruyter 2019-12-01
Series:Open Chemistry
Subjects:
Online Access:https://doi.org/10.1515/chem-2019-0127
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spelling doaj-edad243a5a804007b4fbff7e04897da42021-09-06T19:19:36ZengDe GruyterOpen Chemistry2391-54202019-12-011711157116610.1515/chem-2019-0127chem-2019-0127Increasing the activity of DNAzyme based on the telomeric sequence: 2’-OMe-RNA and LNA modificationsKosman J.0Żukowski K.1Juskowiak B.2Laboratory of Bioanalytical Chemistry, Faculty of Chemistry, Adam Mickiewicz University, Uniwersytetu Poznańskiego 8, 61-614Poznan, PolandLaboratory of Bioanalytical Chemistry, Faculty of Chemistry, Adam Mickiewicz University, Uniwersytetu Poznańskiego 8, 61-614Poznan, PolandLaboratory of Bioanalytical Chemistry, Faculty of Chemistry, Adam Mickiewicz University, Uniwersytetu Poznańskiego 8, 61-614Poznan, Poland2’-OMe-RNA analogues and LNA point modifications of DNA oligonucleotides were applied for the modulation of the G-quadruplex topology and enhancement of peroxidase activity of the resulting DNAzymes. The effect of the 2’-OMe-RNA analogue was studied for full length modified oligonucleotides with various sequences. In the case of LNA-point modification, we have chosen a telomeric DNA sequence and investigated various numbers of modifications. Our main goal was to prove that the application of these modifications can influence the activity of DNAzyme, especially those, which normally form poor DNAzymes. As an example, we have chosen the telomeric HT22 sequence which is known to form DNAzyme characterized by low activity. In all cases, the DNAzymes formed by a telomeric sequence with the application of the 2’-OMe-RNA analogue as well as LNA-point modification, showed significantly higher peroxidase activity. We were also able to shift the formation of hybrid or antiparallel topology to parallel topology. These results are important for the development of probes for biological applications as well as for the design of probes based on DNA sequences that normally form DNAzymes with low activity. This paper also provides information on how the application of nucleotide analogues can transform the topology of G-quadruplexes.https://doi.org/10.1515/chem-2019-0127dnazyme2’-ome-rnalocked nucleic acidg-quadruplexperoxidase activity
collection DOAJ
language English
format Article
sources DOAJ
author Kosman J.
Żukowski K.
Juskowiak B.
spellingShingle Kosman J.
Żukowski K.
Juskowiak B.
Increasing the activity of DNAzyme based on the telomeric sequence: 2’-OMe-RNA and LNA modifications
Open Chemistry
dnazyme
2’-ome-rna
locked nucleic acid
g-quadruplex
peroxidase activity
author_facet Kosman J.
Żukowski K.
Juskowiak B.
author_sort Kosman J.
title Increasing the activity of DNAzyme based on the telomeric sequence: 2’-OMe-RNA and LNA modifications
title_short Increasing the activity of DNAzyme based on the telomeric sequence: 2’-OMe-RNA and LNA modifications
title_full Increasing the activity of DNAzyme based on the telomeric sequence: 2’-OMe-RNA and LNA modifications
title_fullStr Increasing the activity of DNAzyme based on the telomeric sequence: 2’-OMe-RNA and LNA modifications
title_full_unstemmed Increasing the activity of DNAzyme based on the telomeric sequence: 2’-OMe-RNA and LNA modifications
title_sort increasing the activity of dnazyme based on the telomeric sequence: 2’-ome-rna and lna modifications
publisher De Gruyter
series Open Chemistry
issn 2391-5420
publishDate 2019-12-01
description 2’-OMe-RNA analogues and LNA point modifications of DNA oligonucleotides were applied for the modulation of the G-quadruplex topology and enhancement of peroxidase activity of the resulting DNAzymes. The effect of the 2’-OMe-RNA analogue was studied for full length modified oligonucleotides with various sequences. In the case of LNA-point modification, we have chosen a telomeric DNA sequence and investigated various numbers of modifications. Our main goal was to prove that the application of these modifications can influence the activity of DNAzyme, especially those, which normally form poor DNAzymes. As an example, we have chosen the telomeric HT22 sequence which is known to form DNAzyme characterized by low activity. In all cases, the DNAzymes formed by a telomeric sequence with the application of the 2’-OMe-RNA analogue as well as LNA-point modification, showed significantly higher peroxidase activity. We were also able to shift the formation of hybrid or antiparallel topology to parallel topology. These results are important for the development of probes for biological applications as well as for the design of probes based on DNA sequences that normally form DNAzymes with low activity. This paper also provides information on how the application of nucleotide analogues can transform the topology of G-quadruplexes.
topic dnazyme
2’-ome-rna
locked nucleic acid
g-quadruplex
peroxidase activity
url https://doi.org/10.1515/chem-2019-0127
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AT zukowskik increasingtheactivityofdnazymebasedonthetelomericsequence2omernaandlnamodifications
AT juskowiakb increasingtheactivityofdnazymebasedonthetelomericsequence2omernaandlnamodifications
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