Study of alkaloid berberine and its interaction with the human telomeric i-motif DNA structure

[Display omitted] •The interaction of fluorescent ligands with folded DNAs is studied.•Alkaloid berberine binds equally to folded and unfolded cytosine-rich DNA sequences.•Binding with i-motif structures is weak and electrostatics in nature. The alkaloid berberine presents many biological activities...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy Molecular and biomolecular spectroscopy, 2021-03, Vol.248, p.119185, Article 119185
Hauptverfasser: Gargallo, R., Aviñó, A., Eritja, R., Jarosova, P., Mazzini, S., Scaglioni, L., Taborsky, P.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue
container_start_page 119185
container_title Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy
container_volume 248
creator Gargallo, R.
Aviñó, A.
Eritja, R.
Jarosova, P.
Mazzini, S.
Scaglioni, L.
Taborsky, P.
description [Display omitted] •The interaction of fluorescent ligands with folded DNAs is studied.•Alkaloid berberine binds equally to folded and unfolded cytosine-rich DNA sequences.•Binding with i-motif structures is weak and electrostatics in nature. The alkaloid berberine presents many biological activities related to its potential to bind DNA structures, such as duplex or G-quadruplex. Recently, it has been proposed that berberine may interact with i-motif structures formed from the folding of cytosine-rich sequences. In the present work, the interaction of this alkaloid with the i-motif formed by the human telomere cytosine-rich sequence, as well as with several positive and negative controls, has been studied. Molecular fluorescence and circular dichroism spectroscopies, as well as nuclear magnetic resonance spectrometry and competitive dialysis, have been used with this purpose. The results shown here reveal that the interaction of berberine with this i-motif is weak, mostly electrostatics in nature and takes place with bases not involved in C·C+ base pairs. Moreover, this ligand is not selective for i-motif structures, as binds equally to both, folded structure, and unfolded strand, without producing any stabilization of the i-motif. As a conclusion, the development of analytical methods based on the interaction of fluorescent ligands, such as berberine, with i-motif structures should consider the thermodynamic aspects related with the interaction, as well as the selectivity of the proposed ligands with different DNA structures, including unfolded strands.
doi_str_mv 10.1016/j.saa.2020.119185
format Article
fullrecord <record><control><sourceid>pubmed_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1016_j_saa_2020_119185</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1386142520311641</els_id><sourcerecordid>33234477</sourcerecordid><originalsourceid>FETCH-LOGICAL-c396t-40f31962267caeada066cc1246467239c2217e82be457bf9f31745d37261a8503</originalsourceid><addsrcrecordid>eNp9kNtKxDAQhoMorq4-gDeSF-iaU5MWr5b1CIteqLeGNJ2yWbftkqTKvr1Zql4KAzMD3z8MH0IXlMwoofJqPQvGzBhhaaclLfIDdEILxTOe5-owzbyQGRUsn6DTENaEEFowcowmnDMuhFIn6P0lDvUO9w02mw-z6V2NK_CpXAfYdDV2MWDXRfDGRtd3-MvFFY4rwKuhNR2OsOnbRFvssraPrsE3T3Mcoh9sHDycoaPGbAKc__Qperu7fV08ZMvn-8fFfJlZXsqYCdJwWkrGpLIGTG2IlNZSJqSQivHSMkYVFKwCkauqKROtRF5zxSQ1RU74FNHxrvV9CB4avfWuNX6nKdF7V3qtkyu9d6VHVylzOWa2Q9VC_Zf4lZOA6xGA9PmnA6-DddBZqJ0HG3Xdu3_OfwMoM3k0</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Study of alkaloid berberine and its interaction with the human telomeric i-motif DNA structure</title><source>MEDLINE</source><source>ScienceDirect Journals (5 years ago - present)</source><creator>Gargallo, R. ; Aviñó, A. ; Eritja, R. ; Jarosova, P. ; Mazzini, S. ; Scaglioni, L. ; Taborsky, P.</creator><creatorcontrib>Gargallo, R. ; Aviñó, A. ; Eritja, R. ; Jarosova, P. ; Mazzini, S. ; Scaglioni, L. ; Taborsky, P.</creatorcontrib><description>[Display omitted] •The interaction of fluorescent ligands with folded DNAs is studied.•Alkaloid berberine binds equally to folded and unfolded cytosine-rich DNA sequences.•Binding with i-motif structures is weak and electrostatics in nature. The alkaloid berberine presents many biological activities related to its potential to bind DNA structures, such as duplex or G-quadruplex. Recently, it has been proposed that berberine may interact with i-motif structures formed from the folding of cytosine-rich sequences. In the present work, the interaction of this alkaloid with the i-motif formed by the human telomere cytosine-rich sequence, as well as with several positive and negative controls, has been studied. Molecular fluorescence and circular dichroism spectroscopies, as well as nuclear magnetic resonance spectrometry and competitive dialysis, have been used with this purpose. The results shown here reveal that the interaction of berberine with this i-motif is weak, mostly electrostatics in nature and takes place with bases not involved in C·C+ base pairs. Moreover, this ligand is not selective for i-motif structures, as binds equally to both, folded structure, and unfolded strand, without producing any stabilization of the i-motif. As a conclusion, the development of analytical methods based on the interaction of fluorescent ligands, such as berberine, with i-motif structures should consider the thermodynamic aspects related with the interaction, as well as the selectivity of the proposed ligands with different DNA structures, including unfolded strands.</description><identifier>ISSN: 1386-1425</identifier><identifier>EISSN: 1873-3557</identifier><identifier>DOI: 10.1016/j.saa.2020.119185</identifier><identifier>PMID: 33234477</identifier><language>eng</language><publisher>England: Elsevier B.V</publisher><subject>Alkaloids ; Berberine ; Circular Dichroism ; DNA ; DNA binders ; G-quadruplex ; G-Quadruplexes ; Humans ; I-motif ; Renal Dialysis ; Telomere</subject><ispartof>Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 2021-03, Vol.248, p.119185, Article 119185</ispartof><rights>2020 Elsevier B.V.</rights><rights>Copyright © 2020 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c396t-40f31962267caeada066cc1246467239c2217e82be457bf9f31745d37261a8503</citedby><cites>FETCH-LOGICAL-c396t-40f31962267caeada066cc1246467239c2217e82be457bf9f31745d37261a8503</cites><orcidid>0000-0001-8716-8356 ; 0000-0002-3553-9036 ; 0000-0001-5383-9334</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.saa.2020.119185$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33234477$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gargallo, R.</creatorcontrib><creatorcontrib>Aviñó, A.</creatorcontrib><creatorcontrib>Eritja, R.</creatorcontrib><creatorcontrib>Jarosova, P.</creatorcontrib><creatorcontrib>Mazzini, S.</creatorcontrib><creatorcontrib>Scaglioni, L.</creatorcontrib><creatorcontrib>Taborsky, P.</creatorcontrib><title>Study of alkaloid berberine and its interaction with the human telomeric i-motif DNA structure</title><title>Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy</title><addtitle>Spectrochim Acta A Mol Biomol Spectrosc</addtitle><description>[Display omitted] •The interaction of fluorescent ligands with folded DNAs is studied.•Alkaloid berberine binds equally to folded and unfolded cytosine-rich DNA sequences.•Binding with i-motif structures is weak and electrostatics in nature. The alkaloid berberine presents many biological activities related to its potential to bind DNA structures, such as duplex or G-quadruplex. Recently, it has been proposed that berberine may interact with i-motif structures formed from the folding of cytosine-rich sequences. In the present work, the interaction of this alkaloid with the i-motif formed by the human telomere cytosine-rich sequence, as well as with several positive and negative controls, has been studied. Molecular fluorescence and circular dichroism spectroscopies, as well as nuclear magnetic resonance spectrometry and competitive dialysis, have been used with this purpose. The results shown here reveal that the interaction of berberine with this i-motif is weak, mostly electrostatics in nature and takes place with bases not involved in C·C+ base pairs. Moreover, this ligand is not selective for i-motif structures, as binds equally to both, folded structure, and unfolded strand, without producing any stabilization of the i-motif. As a conclusion, the development of analytical methods based on the interaction of fluorescent ligands, such as berberine, with i-motif structures should consider the thermodynamic aspects related with the interaction, as well as the selectivity of the proposed ligands with different DNA structures, including unfolded strands.</description><subject>Alkaloids</subject><subject>Berberine</subject><subject>Circular Dichroism</subject><subject>DNA</subject><subject>DNA binders</subject><subject>G-quadruplex</subject><subject>G-Quadruplexes</subject><subject>Humans</subject><subject>I-motif</subject><subject>Renal Dialysis</subject><subject>Telomere</subject><issn>1386-1425</issn><issn>1873-3557</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kNtKxDAQhoMorq4-gDeSF-iaU5MWr5b1CIteqLeGNJ2yWbftkqTKvr1Zql4KAzMD3z8MH0IXlMwoofJqPQvGzBhhaaclLfIDdEILxTOe5-owzbyQGRUsn6DTENaEEFowcowmnDMuhFIn6P0lDvUO9w02mw-z6V2NK_CpXAfYdDV2MWDXRfDGRtd3-MvFFY4rwKuhNR2OsOnbRFvssraPrsE3T3Mcoh9sHDycoaPGbAKc__Qperu7fV08ZMvn-8fFfJlZXsqYCdJwWkrGpLIGTG2IlNZSJqSQivHSMkYVFKwCkauqKROtRF5zxSQ1RU74FNHxrvV9CB4avfWuNX6nKdF7V3qtkyu9d6VHVylzOWa2Q9VC_Zf4lZOA6xGA9PmnA6-DddBZqJ0HG3Xdu3_OfwMoM3k0</recordid><startdate>20210305</startdate><enddate>20210305</enddate><creator>Gargallo, R.</creator><creator>Aviñó, A.</creator><creator>Eritja, R.</creator><creator>Jarosova, P.</creator><creator>Mazzini, S.</creator><creator>Scaglioni, L.</creator><creator>Taborsky, P.</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0001-8716-8356</orcidid><orcidid>https://orcid.org/0000-0002-3553-9036</orcidid><orcidid>https://orcid.org/0000-0001-5383-9334</orcidid></search><sort><creationdate>20210305</creationdate><title>Study of alkaloid berberine and its interaction with the human telomeric i-motif DNA structure</title><author>Gargallo, R. ; Aviñó, A. ; Eritja, R. ; Jarosova, P. ; Mazzini, S. ; Scaglioni, L. ; Taborsky, P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c396t-40f31962267caeada066cc1246467239c2217e82be457bf9f31745d37261a8503</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Alkaloids</topic><topic>Berberine</topic><topic>Circular Dichroism</topic><topic>DNA</topic><topic>DNA binders</topic><topic>G-quadruplex</topic><topic>G-Quadruplexes</topic><topic>Humans</topic><topic>I-motif</topic><topic>Renal Dialysis</topic><topic>Telomere</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gargallo, R.</creatorcontrib><creatorcontrib>Aviñó, A.</creatorcontrib><creatorcontrib>Eritja, R.</creatorcontrib><creatorcontrib>Jarosova, P.</creatorcontrib><creatorcontrib>Mazzini, S.</creatorcontrib><creatorcontrib>Scaglioni, L.</creatorcontrib><creatorcontrib>Taborsky, P.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gargallo, R.</au><au>Aviñó, A.</au><au>Eritja, R.</au><au>Jarosova, P.</au><au>Mazzini, S.</au><au>Scaglioni, L.</au><au>Taborsky, P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Study of alkaloid berberine and its interaction with the human telomeric i-motif DNA structure</atitle><jtitle>Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy</jtitle><addtitle>Spectrochim Acta A Mol Biomol Spectrosc</addtitle><date>2021-03-05</date><risdate>2021</risdate><volume>248</volume><spage>119185</spage><pages>119185-</pages><artnum>119185</artnum><issn>1386-1425</issn><eissn>1873-3557</eissn><abstract>[Display omitted] •The interaction of fluorescent ligands with folded DNAs is studied.•Alkaloid berberine binds equally to folded and unfolded cytosine-rich DNA sequences.•Binding with i-motif structures is weak and electrostatics in nature. The alkaloid berberine presents many biological activities related to its potential to bind DNA structures, such as duplex or G-quadruplex. Recently, it has been proposed that berberine may interact with i-motif structures formed from the folding of cytosine-rich sequences. In the present work, the interaction of this alkaloid with the i-motif formed by the human telomere cytosine-rich sequence, as well as with several positive and negative controls, has been studied. Molecular fluorescence and circular dichroism spectroscopies, as well as nuclear magnetic resonance spectrometry and competitive dialysis, have been used with this purpose. The results shown here reveal that the interaction of berberine with this i-motif is weak, mostly electrostatics in nature and takes place with bases not involved in C·C+ base pairs. Moreover, this ligand is not selective for i-motif structures, as binds equally to both, folded structure, and unfolded strand, without producing any stabilization of the i-motif. As a conclusion, the development of analytical methods based on the interaction of fluorescent ligands, such as berberine, with i-motif structures should consider the thermodynamic aspects related with the interaction, as well as the selectivity of the proposed ligands with different DNA structures, including unfolded strands.</abstract><cop>England</cop><pub>Elsevier B.V</pub><pmid>33234477</pmid><doi>10.1016/j.saa.2020.119185</doi><orcidid>https://orcid.org/0000-0001-8716-8356</orcidid><orcidid>https://orcid.org/0000-0002-3553-9036</orcidid><orcidid>https://orcid.org/0000-0001-5383-9334</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1386-1425
ispartof Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 2021-03, Vol.248, p.119185, Article 119185
issn 1386-1425
1873-3557
language eng
recordid cdi_crossref_primary_10_1016_j_saa_2020_119185
source MEDLINE; ScienceDirect Journals (5 years ago - present)
subjects Alkaloids
Berberine
Circular Dichroism
DNA
DNA binders
G-quadruplex
G-Quadruplexes
Humans
I-motif
Renal Dialysis
Telomere
title Study of alkaloid berberine and its interaction with the human telomeric i-motif DNA structure
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T20%3A58%3A40IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmed_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Study%20of%20alkaloid%20berberine%20and%20its%20interaction%20with%20the%20human%20telomeric%20i-motif%20DNA%20structure&rft.jtitle=Spectrochimica%20acta.%20Part%20A,%20Molecular%20and%20biomolecular%20spectroscopy&rft.au=Gargallo,%20R.&rft.date=2021-03-05&rft.volume=248&rft.spage=119185&rft.pages=119185-&rft.artnum=119185&rft.issn=1386-1425&rft.eissn=1873-3557&rft_id=info:doi/10.1016/j.saa.2020.119185&rft_dat=%3Cpubmed_cross%3E33234477%3C/pubmed_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/33234477&rft_els_id=S1386142520311641&rfr_iscdi=true