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Evaluation of newly synthesised benzo[a]phenoxazinium chlorides as fluorescent probes using Saccharomyces cerevisiae as model organism

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Resumo:The potential as fluorescent probes of two recently synthesised water-soluble benzo[a]phenoxazinium salts, mono- or dissubstituted with carboxylic ester groups as terminal of propyl substituents at the amine of position 9, were studied by fluorescence microscopy employing intact, live cells. With the aim of assessing the compounds cellular staining pattern and potential specificity, co-localization experiments were performed using yeast mutants expressing green fluorescent protein (GFP)-tagged proteins that localize to specific intracellular location/organelles. It was found that both compounds display a very high affinity for the vacuolar membrane, being the dissubstituted compound especially important due to its higher fluorescence at lower, less toxic concentrations.
Autores principais:Leitão, Maria Inês
Outros Autores:Raju, B. Rama; Sousa, Maria João; Gonçalves, M. Sameiro T.
Assunto:NIR fluorescent probes Nile Blue Benzo[a]phenoxazine derivatives Fluorescence microscopy
Ano:2014
País:Portugal
Tipo de documento:comunicação em conferência
Tipo de acesso:acesso restrito
Instituição associada:Universidade do Minho
Idioma:inglês
Origem:RepositóriUM - Universidade do Minho
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author Leitão, Maria Inês
author2 Raju, B. Rama
Sousa, Maria João
Gonçalves, M. Sameiro T.
author2_role author
author
author
author_facet Leitão, Maria Inês
Raju, B. Rama
Sousa, Maria João
Gonçalves, M. Sameiro T.
author_role author
contributor_name_str_mv Universidade do Minho
country_str PT
creators_json_txt [{\"Person.name\":\"Leitão, Maria Inês\"},{\"Person.name\":\"Raju, B. Rama\"},{\"Person.name\":\"Sousa, Maria João\"},{\"Person.name\":\"Gonçalves, M. Sameiro T.\"}]
datacite.contributors.contributor.contributorName.fl_str_mv Universidade do Minho
datacite.creators.creator.creatorName.fl_str_mv Leitão, Maria Inês
Raju, B. Rama
Sousa, Maria João
Gonçalves, M. Sameiro T.
datacite.date.Accepted.fl_str_mv 2014-01-01T00:00:00Z
datacite.date.available.fl_str_mv 2014-12-04T12:39:59Z
datacite.date.embargoed.fl_str_mv 2014-12-04T12:39:59Z
datacite.rights.fl_str_mv http://purl.org/coar/access_right/c_16ec
datacite.subjects.subject.fl_str_mv NIR fluorescent probes
Nile Blue
Benzo[a]phenoxazine derivatives
Fluorescence microscopy
datacite.titles.title.fl_str_mv Evaluation of newly synthesised benzo[a]phenoxazinium chlorides as fluorescent probes using Saccharomyces cerevisiae as model organism
dc.contributor.none.fl_str_mv Universidade do Minho
dc.creator.none.fl_str_mv Leitão, Maria Inês
Raju, B. Rama
Sousa, Maria João
Gonçalves, M. Sameiro T.
dc.date.Accepted.fl_str_mv 2014-01-01T00:00:00Z
dc.date.available.fl_str_mv 2014-12-04T12:39:59Z
dc.date.embargoed.fl_str_mv 2014-12-04T12:39:59Z
dc.format.none.fl_str_mv application/pdf
dc.identifier.none.fl_str_mv https://hdl.handle.net/1822/31614
dc.language.none.fl_str_mv eng
dc.rights.none.fl_str_mv http://purl.org/coar/access_right/c_16ec
dc.subject.none.fl_str_mv NIR fluorescent probes
Nile Blue
Benzo[a]phenoxazine derivatives
Fluorescence microscopy
dc.title.fl_str_mv Evaluation of newly synthesised benzo[a]phenoxazinium chlorides as fluorescent probes using Saccharomyces cerevisiae as model organism
dc.type.none.fl_str_mv http://purl.org/coar/resource_type/c_5794
description The potential as fluorescent probes of two recently synthesised water-soluble benzo[a]phenoxazinium salts, mono- or dissubstituted with carboxylic ester groups as terminal of propyl substituents at the amine of position 9, were studied by fluorescence microscopy employing intact, live cells. With the aim of assessing the compounds cellular staining pattern and potential specificity, co-localization experiments were performed using yeast mutants expressing green fluorescent protein (GFP)-tagged proteins that localize to specific intracellular location/organelles. It was found that both compounds display a very high affinity for the vacuolar membrane, being the dissubstituted compound especially important due to its higher fluorescence at lower, less toxic concentrations.
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eu_rights_str_mv restrictedAccess
format conferencePaper
fulltext.url.fl_str_mv https://prod-dspace.uminho.pt/bitstreams/9d226558-9c18-4ee2-9846-be34c6657d79/download
id rum_2ade6087ca3b6c2c6005e40335c8feb4
identifier.url.fl_str_mv https://hdl.handle.net/1822/31614
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:1822/31614
organization_str_mv urn:organizationAcronym:repositorium
person_str_mv Leitão, Maria Inês
Raju, B. Rama
Sousa, Maria João
Gonçalves, M. Sameiro T.
publishDate 2014
reponame_str RepositóriUM - Universidade do Minho
repository_id_str urn:repositoryAcronym:rum
service_str_mv urn:repositoryAcronym:rum
spelling engporThe potential as fluorescent probes of two recently synthesised water-soluble benzo[a]phenoxazinium salts, mono- or dissubstituted with carboxylic ester groups as terminal of propyl substituents at the amine of position 9, were studied by fluorescence microscopy employing intact, live cells. With the aim of assessing the compounds cellular staining pattern and potential specificity, co-localization experiments were performed using yeast mutants expressing green fluorescent protein (GFP)-tagged proteins that localize to specific intracellular location/organelles. It was found that both compounds display a very high affinity for the vacuolar membrane, being the dissubstituted compound especially important due to its higher fluorescence at lower, less toxic concentrations.application/pdfporEvaluation of newly synthesised benzo[a]phenoxazinium chlorides as fluorescent probes using Saccharomyces cerevisiae as model organismLeitão, Maria InêsRaju, B. RamaSousa, Maria JoãoGonçalves, M. Sameiro T.HostingInstitutionOrganizationalUniversidade do Minhoe-mailmailto:repositorium@usdb.uminho.ptrepositorium@usdb.uminho.ptDOIIsPartOf10.3390/ecsoc-18-b0212014-12-04T12:39:59Z20142014-01-01T00:00:00ZHandlehttps://hdl.handle.net/1822/31614http://purl.org/coar/access_right/c_16ecrestricted accessNIR fluorescent probesNile BlueBenzo[a]phenoxazine derivativesFluorescence microscopy245914 bytesother research producthttp://purl.org/coar/resource_type/c_5794conference paperhttp://purl.org/coar/access_right/c_16ecapplication/pdffulltexthttps://prod-dspace.uminho.pt/bitstreams/9d226558-9c18-4ee2-9846-be34c6657d79/download
spellingShingle Evaluation of newly synthesised benzo[a]phenoxazinium chlorides as fluorescent probes using Saccharomyces cerevisiae as model organism
Leitão, Maria Inês
NIR fluorescent probes
Nile Blue
Benzo[a]phenoxazine derivatives
Fluorescence microscopy
status SINGLETON
subject.fl_str_mv NIR fluorescent probes
Nile Blue
Benzo[a]phenoxazine derivatives
Fluorescence microscopy
title Evaluation of newly synthesised benzo[a]phenoxazinium chlorides as fluorescent probes using Saccharomyces cerevisiae as model organism
title_full Evaluation of newly synthesised benzo[a]phenoxazinium chlorides as fluorescent probes using Saccharomyces cerevisiae as model organism
title_fullStr Evaluation of newly synthesised benzo[a]phenoxazinium chlorides as fluorescent probes using Saccharomyces cerevisiae as model organism
title_full_unstemmed Evaluation of newly synthesised benzo[a]phenoxazinium chlorides as fluorescent probes using Saccharomyces cerevisiae as model organism
title_short Evaluation of newly synthesised benzo[a]phenoxazinium chlorides as fluorescent probes using Saccharomyces cerevisiae as model organism
title_sort Evaluation of newly synthesised benzo[a]phenoxazinium chlorides as fluorescent probes using Saccharomyces cerevisiae as model organism
topic NIR fluorescent probes
Nile Blue
Benzo[a]phenoxazine derivatives
Fluorescence microscopy
topic_facet NIR fluorescent probes
Nile Blue
Benzo[a]phenoxazine derivatives
Fluorescence microscopy
url https://hdl.handle.net/1822/31614
visible 1