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Fluorescence studies of the interaction of pyrenylmethyl tributylphosphonium bromide with double-strand polynucleotides

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Resumo:The interaction between pyren-1-ylmethyl tri-n-butylphosphonium bromide (PMTP), a water-soluble cationic pyrene derivative and the double-strand polynucleotides Poly[dA-dT], Poly[dA].Poly[dT], Poly[dG-dC] and Poly[dG]. Poly[dC] was studied using UV-Vis absorption and fluorescence spectroscopy. The PMTP probe interacts with polynucleotides through both weak and intercalative binding, evidenced through changes in the absorption spectrum (hypochromicity and red shift). The two binding types were distinguished using time-resolved fluorescence, as the intercalative environment differs from that of the surface. Thymine and cytosine are more efficient quenchers of PMTP situated on the surface because of the higher proton accessibility to this region. In contrast, adenine does not quench PMTP fluorescence, whereas guanine residues are always very efficient quenching sites. Therefore, through the use of spectroscopic techniques, it was possible to obtain information concerning the partition of PMTP in each form of binding. In the heteropolymers, Poly[dA-dT] and Poly[dG-dC], PMTP exhibits a significant preference for intercalation in AT sequences, while with GC, the intercalation is lower. In the homopolymers, Poly[dA].Poly[dT] and Poly[dG].Poly[dC], the main mechanism of interaction is weak binding, but some base preferences are elucidated. Additionally, Poly[dA].Poly[dT] can be distinguished from Poly[dA-dT] through a direct energy-transfer process between several bound PMTP molecules.
Autores principais:Oliveira, M. Elisabete
Outros Autores:Baptista, Adelina L. F.; Coutinho, Paulo J. G.; Castanheira, Elisabete M. S.; Hungerford, Graham
Assunto:Polynucleotides Fluorescence Pyrene derivatives
Ano:2004
País:Portugal
Tipo de documento:artigo
Tipo de acesso:acesso aberto
Instituição associada:Universidade do Minho
Idioma:inglês
Origem:RepositóriUM - Universidade do Minho
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author Oliveira, M. Elisabete
author2 Baptista, Adelina L. F.
Coutinho, Paulo J. G.
Castanheira, Elisabete M. S.
Hungerford, Graham
author2_role author
author
author
author
author_facet Oliveira, M. Elisabete
Baptista, Adelina L. F.
Coutinho, Paulo J. G.
Castanheira, Elisabete M. S.
Hungerford, Graham
author_role author
contributor_name_str_mv RepositóriUM - Universidade do Minho
country_str PT
creators_json_txt [{\"Person.name\":\"Oliveira, M. Elisabete\"},{\"Person.name\":\"Baptista, Adelina L. F.\"},{\"Person.name\":\"Coutinho, Paulo J. G.\"},{\"Person.name\":\"Castanheira, Elisabete M. S.\"},{\"Person.name\":\"Hungerford, Graham\"}]
datacite.contributors.contributor.contributorName.fl_str_mv RepositóriUM - Universidade do Minho
datacite.creators.creator.creatorName.fl_str_mv Oliveira, M. Elisabete
Baptista, Adelina L. F.
Coutinho, Paulo J. G.
Castanheira, Elisabete M. S.
Hungerford, Graham
datacite.date.Accepted.fl_str_mv 2004-01-01T00:00:00Z
datacite.date.available.fl_str_mv 2006-06-21T14:16:35Z
datacite.date.embargoed.fl_str_mv 2006-06-21T14:16:35Z
datacite.rights.fl_str_mv http://purl.org/coar/access_right/c_abf2
datacite.subjects.subject.fl_str_mv Polynucleotides
Fluorescence
Pyrene derivatives
datacite.titles.title.fl_str_mv Fluorescence studies of the interaction of pyrenylmethyl tributylphosphonium bromide with double-strand polynucleotides
dc.contributor.none.fl_str_mv RepositóriUM - Universidade do Minho
dc.creator.none.fl_str_mv Oliveira, M. Elisabete
Baptista, Adelina L. F.
Coutinho, Paulo J. G.
Castanheira, Elisabete M. S.
Hungerford, Graham
dc.date.Accepted.fl_str_mv 2004-01-01T00:00:00Z
dc.date.available.fl_str_mv 2006-06-21T14:16:35Z
dc.date.embargoed.fl_str_mv 2006-06-21T14:16:35Z
dc.format.none.fl_str_mv application/pdf
dc.identifier.none.fl_str_mv https://hdl.handle.net/1822/5141
dc.language.none.fl_str_mv eng
dc.publisher.none.fl_str_mv Royal Society of Chemistry
dc.rights.none.fl_str_mv http://purl.org/coar/access_right/c_abf2
dc.subject.none.fl_str_mv Polynucleotides
Fluorescence
Pyrene derivatives
dc.title.fl_str_mv Fluorescence studies of the interaction of pyrenylmethyl tributylphosphonium bromide with double-strand polynucleotides
dc.type.none.fl_str_mv http://purl.org/coar/resource_type/c_6501
description The interaction between pyren-1-ylmethyl tri-n-butylphosphonium bromide (PMTP), a water-soluble cationic pyrene derivative and the double-strand polynucleotides Poly[dA-dT], Poly[dA].Poly[dT], Poly[dG-dC] and Poly[dG]. Poly[dC] was studied using UV-Vis absorption and fluorescence spectroscopy. The PMTP probe interacts with polynucleotides through both weak and intercalative binding, evidenced through changes in the absorption spectrum (hypochromicity and red shift). The two binding types were distinguished using time-resolved fluorescence, as the intercalative environment differs from that of the surface. Thymine and cytosine are more efficient quenchers of PMTP situated on the surface because of the higher proton accessibility to this region. In contrast, adenine does not quench PMTP fluorescence, whereas guanine residues are always very efficient quenching sites. Therefore, through the use of spectroscopic techniques, it was possible to obtain information concerning the partition of PMTP in each form of binding. In the heteropolymers, Poly[dA-dT] and Poly[dG-dC], PMTP exhibits a significant preference for intercalation in AT sequences, while with GC, the intercalation is lower. In the homopolymers, Poly[dA].Poly[dT] and Poly[dG].Poly[dC], the main mechanism of interaction is weak binding, but some base preferences are elucidated. Additionally, Poly[dA].Poly[dT] can be distinguished from Poly[dA-dT] through a direct energy-transfer process between several bound PMTP molecules.
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eu_rights_str_mv openAccess
format article
fulltext.url.fl_str_mv https://repositorium.uminho.pt/bitstreams/213b4046-4681-4f40-aba4-db207671f35d/download
id rum_7fa1efd9da77958b8f5f2d3d93236ef7
identifier.url.fl_str_mv https://hdl.handle.net/1822/5141
instacron_str repositorium
institution Universidade do Minho
instname_str Universidade do Minho
language eng
network_acronym_str rum
network_name_str RepositóriUM - Universidade do Minho
oai_identifier_str oai:repositorium.uminho.pt:1822/5141
organization_str_mv urn:organizationAcronym:repositorium
person_str_mv Oliveira, M. Elisabete
Baptista, Adelina L. F.
Coutinho, Paulo J. G.
Castanheira, Elisabete M. S.
Hungerford, Graham
publishDate 2004
publisher.none.fl_str_mv Royal Society of Chemistry
reponame_str RepositóriUM - Universidade do Minho
repository_id_str urn:repositoryAcronym:rum
service_str_mv urn:repositoryAcronym:rum
spelling engRoyal Society of ChemistryengThe interaction between pyren-1-ylmethyl tri-n-butylphosphonium bromide (PMTP), a water-soluble cationic pyrene derivative and the double-strand polynucleotides Poly[dA-dT], Poly[dA].Poly[dT], Poly[dG-dC] and Poly[dG]. Poly[dC] was studied using UV-Vis absorption and fluorescence spectroscopy. The PMTP probe interacts with polynucleotides through both weak and intercalative binding, evidenced through changes in the absorption spectrum (hypochromicity and red shift). The two binding types were distinguished using time-resolved fluorescence, as the intercalative environment differs from that of the surface. Thymine and cytosine are more efficient quenchers of PMTP situated on the surface because of the higher proton accessibility to this region. In contrast, adenine does not quench PMTP fluorescence, whereas guanine residues are always very efficient quenching sites. Therefore, through the use of spectroscopic techniques, it was possible to obtain information concerning the partition of PMTP in each form of binding. In the heteropolymers, Poly[dA-dT] and Poly[dG-dC], PMTP exhibits a significant preference for intercalation in AT sequences, while with GC, the intercalation is lower. In the homopolymers, Poly[dA].Poly[dT] and Poly[dG].Poly[dC], the main mechanism of interaction is weak binding, but some base preferences are elucidated. Additionally, Poly[dA].Poly[dT] can be distinguished from Poly[dA-dT] through a direct energy-transfer process between several bound PMTP molecules.application/pdfengFluorescence studies of the interaction of pyrenylmethyl tributylphosphonium bromide with double-strand polynucleotidesOliveira, M. ElisabeteBaptista, Adelina L. F.Coutinho, Paulo J. G.Castanheira, Elisabete M. S.Hungerford, GrahamHostingInstitutionOrganizationalRepositóriUM - Universidade do Minhoe-mailmailto:repositorium@usdb.uminho.ptrepositorium@usdb.uminho.ptCITATION"Photochemical & Photobiological Sciences". ISSN 1474-905X. 3:2 (2004) 217-225.PMID14872240ISSNIsPartOf1474-905XDOIIsPartOf10.1039/b305225g2006-06-21T14:16:35Z20042004-01-01T00:00:00ZHandlehttps://hdl.handle.net/1822/5141http://purl.org/coar/access_right/c_abf2open accessPolynucleotidesFluorescencePyrene derivatives210058 bytesliteraturehttp://purl.org/coar/resource_type/c_6501journal articlehttp://purl.org/coar/access_right/c_abf2application/pdffulltexthttps://repositorium.uminho.pt/bitstreams/213b4046-4681-4f40-aba4-db207671f35d/download
spellingShingle Fluorescence studies of the interaction of pyrenylmethyl tributylphosphonium bromide with double-strand polynucleotides
Oliveira, M. Elisabete
Polynucleotides
Fluorescence
Pyrene derivatives
status SINGLETON
subject.fl_str_mv Polynucleotides
Fluorescence
Pyrene derivatives
title Fluorescence studies of the interaction of pyrenylmethyl tributylphosphonium bromide with double-strand polynucleotides
title_full Fluorescence studies of the interaction of pyrenylmethyl tributylphosphonium bromide with double-strand polynucleotides
title_fullStr Fluorescence studies of the interaction of pyrenylmethyl tributylphosphonium bromide with double-strand polynucleotides
title_full_unstemmed Fluorescence studies of the interaction of pyrenylmethyl tributylphosphonium bromide with double-strand polynucleotides
title_short Fluorescence studies of the interaction of pyrenylmethyl tributylphosphonium bromide with double-strand polynucleotides
title_sort Fluorescence studies of the interaction of pyrenylmethyl tributylphosphonium bromide with double-strand polynucleotides
topic Polynucleotides
Fluorescence
Pyrene derivatives
topic_facet Polynucleotides
Fluorescence
Pyrene derivatives
url https://hdl.handle.net/1822/5141
visible 1