RNA and DNA aptamers in cytomics analysis

Detalhes bibliográficos
Autor(a) principal: Ulrich, H.
Data de Publicação: 2004
Outros Autores: Martins, Antonio Henrique Baccin [UNIFESP], Pesquero, Joao Bosco [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://repositorio.unifesp.br/handle/11600/27766
http://dx.doi.org/10.1002/cyto.a.20056
Resumo: Background: the systematic evolution of ligands by exponential enrichment (SELEX) technique is a combinatorial library approach in which DNA or RNA molecules (aptamers) are selected by their ability to bind their protein targets with high affinity and specificity, comparable to that of monoclonal antibodies. in contrast to antibodies conventionally selected in animals, aptamers are generated by an in vitro selection process, and can be directed against almost every target, including antigens like toxins or nonimmunogenic targets, against which conventional antibodies cannot be raised.Methods: Aptamers are ideal candidates for cytomics, as they can be attached to fluorescent reporters or nanoparticles in order to study biological function by fluorescence microscopy, by flow cytometry, or to quantify the concentration of their target in biological fluids or cells using ELISA, RIA, and Western blot assays.Results: We demonstrate the in vitro selection of antikinin B1 receptor aptamers that could be used to determine B1 receptor expression during inflammation processes. These aptamers specifically recognize their target in a Northern-Western blot assay, and bind to their target protein whenever they are exposed in the membrane.Conclusions: Currently, aptamers are linked to fluorescent reporters. We discuss here the present status and future directions concerning the use of the SELEX technique in cytomics. (C) 2004 Wiley-Liss, Inc.
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spelling Ulrich, H.Martins, Antonio Henrique Baccin [UNIFESP]Pesquero, Joao Bosco [UNIFESP]Universidade de São Paulo (USP)Universidade Federal de São Paulo (UNIFESP)2016-01-24T12:37:10Z2016-01-24T12:37:10Z2004-06-01Cytometry Part A. Hoboken: Wiley-liss, v. 59A, n. 2, p. 220-231, 2004.0196-4763http://repositorio.unifesp.br/handle/11600/27766http://dx.doi.org/10.1002/cyto.a.2005610.1002/cyto.a.20056WOS:000221855700007Background: the systematic evolution of ligands by exponential enrichment (SELEX) technique is a combinatorial library approach in which DNA or RNA molecules (aptamers) are selected by their ability to bind their protein targets with high affinity and specificity, comparable to that of monoclonal antibodies. in contrast to antibodies conventionally selected in animals, aptamers are generated by an in vitro selection process, and can be directed against almost every target, including antigens like toxins or nonimmunogenic targets, against which conventional antibodies cannot be raised.Methods: Aptamers are ideal candidates for cytomics, as they can be attached to fluorescent reporters or nanoparticles in order to study biological function by fluorescence microscopy, by flow cytometry, or to quantify the concentration of their target in biological fluids or cells using ELISA, RIA, and Western blot assays.Results: We demonstrate the in vitro selection of antikinin B1 receptor aptamers that could be used to determine B1 receptor expression during inflammation processes. These aptamers specifically recognize their target in a Northern-Western blot assay, and bind to their target protein whenever they are exposed in the membrane.Conclusions: Currently, aptamers are linked to fluorescent reporters. We discuss here the present status and future directions concerning the use of the SELEX technique in cytomics. (C) 2004 Wiley-Liss, Inc.Univ São Paulo, Inst Quim, Dept Biochem, BR-05599970 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Biophys, BR-05599970 São Paulo, BrazilUniversidade Federal de São Paulo, Dept Biophys, BR-05599970 São Paulo, BrazilWeb of Science220-231engWiley-BlackwellCytometry Part Ahttp://olabout.wiley.com/WileyCDA/Section/id-406071.htmlinfo:eu-repo/semantics/openAccessSELEXcytomicsfluorescent-tagged aptamerskinin B1 receptorNorthern-Western-Blot assayRNA and DNA aptamers in cytomics analysisinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlereponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP11600/277662022-07-08 10:45:09.117metadata only accessoai:repositorio.unifesp.br:11600/27766Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652023-05-25T12:19:47.960118Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.en.fl_str_mv RNA and DNA aptamers in cytomics analysis
title RNA and DNA aptamers in cytomics analysis
spellingShingle RNA and DNA aptamers in cytomics analysis
Ulrich, H.
SELEX
cytomics
fluorescent-tagged aptamers
kinin B1 receptor
Northern-Western-Blot assay
title_short RNA and DNA aptamers in cytomics analysis
title_full RNA and DNA aptamers in cytomics analysis
title_fullStr RNA and DNA aptamers in cytomics analysis
title_full_unstemmed RNA and DNA aptamers in cytomics analysis
title_sort RNA and DNA aptamers in cytomics analysis
author Ulrich, H.
author_facet Ulrich, H.
Martins, Antonio Henrique Baccin [UNIFESP]
Pesquero, Joao Bosco [UNIFESP]
author_role author
author2 Martins, Antonio Henrique Baccin [UNIFESP]
Pesquero, Joao Bosco [UNIFESP]
author2_role author
author
dc.contributor.institution.none.fl_str_mv Universidade de São Paulo (USP)
Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Ulrich, H.
Martins, Antonio Henrique Baccin [UNIFESP]
Pesquero, Joao Bosco [UNIFESP]
dc.subject.eng.fl_str_mv SELEX
cytomics
fluorescent-tagged aptamers
kinin B1 receptor
Northern-Western-Blot assay
topic SELEX
cytomics
fluorescent-tagged aptamers
kinin B1 receptor
Northern-Western-Blot assay
description Background: the systematic evolution of ligands by exponential enrichment (SELEX) technique is a combinatorial library approach in which DNA or RNA molecules (aptamers) are selected by their ability to bind their protein targets with high affinity and specificity, comparable to that of monoclonal antibodies. in contrast to antibodies conventionally selected in animals, aptamers are generated by an in vitro selection process, and can be directed against almost every target, including antigens like toxins or nonimmunogenic targets, against which conventional antibodies cannot be raised.Methods: Aptamers are ideal candidates for cytomics, as they can be attached to fluorescent reporters or nanoparticles in order to study biological function by fluorescence microscopy, by flow cytometry, or to quantify the concentration of their target in biological fluids or cells using ELISA, RIA, and Western blot assays.Results: We demonstrate the in vitro selection of antikinin B1 receptor aptamers that could be used to determine B1 receptor expression during inflammation processes. These aptamers specifically recognize their target in a Northern-Western blot assay, and bind to their target protein whenever they are exposed in the membrane.Conclusions: Currently, aptamers are linked to fluorescent reporters. We discuss here the present status and future directions concerning the use of the SELEX technique in cytomics. (C) 2004 Wiley-Liss, Inc.
publishDate 2004
dc.date.issued.fl_str_mv 2004-06-01
dc.date.accessioned.fl_str_mv 2016-01-24T12:37:10Z
dc.date.available.fl_str_mv 2016-01-24T12:37:10Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.citation.fl_str_mv Cytometry Part A. Hoboken: Wiley-liss, v. 59A, n. 2, p. 220-231, 2004.
dc.identifier.uri.fl_str_mv http://repositorio.unifesp.br/handle/11600/27766
http://dx.doi.org/10.1002/cyto.a.20056
dc.identifier.issn.none.fl_str_mv 0196-4763
dc.identifier.doi.none.fl_str_mv 10.1002/cyto.a.20056
dc.identifier.wos.none.fl_str_mv WOS:000221855700007
identifier_str_mv Cytometry Part A. Hoboken: Wiley-liss, v. 59A, n. 2, p. 220-231, 2004.
0196-4763
10.1002/cyto.a.20056
WOS:000221855700007
url http://repositorio.unifesp.br/handle/11600/27766
http://dx.doi.org/10.1002/cyto.a.20056
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.none.fl_str_mv Cytometry Part A
dc.rights.driver.fl_str_mv http://olabout.wiley.com/WileyCDA/Section/id-406071.html
info:eu-repo/semantics/openAccess
rights_invalid_str_mv http://olabout.wiley.com/WileyCDA/Section/id-406071.html
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 220-231
dc.publisher.none.fl_str_mv Wiley-Blackwell
publisher.none.fl_str_mv Wiley-Blackwell
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv
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