Evidence of native Metal–S2–Metallothionein complexes confirmed by the analysis of Cup1 Divalent-Metal-Ion binding properties

Autores
Orihuela, Rubén; Monteiro, Freddy; Pagani, María Ayelén; Capdevila, Merce; Atrian, Silvia
Año de publicación
2010
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
It has previously been shown that recombinant synthesis, under metal-supplemented conditions, of diverse metallothioneins (MTs) results in the recovery of a subpopulation of S2- containing complexes in addition to the S2-devoid canonical metal–MT species. Further significance of this finding has remained veiled by the possibility of it being a mere consequence of synthesis in a heterologous bacterial system. Herein, we present definitive evidence that S2 ligands are also constituents of native metal–MT complexes. Because, although practically universal, the highest S2 content is incorporated by copper-thioneins when coordinating divalent metal ions, we adapted the Saccharomyces cerevisiae Cup1 protein, which is the most paradigmatic copper-thionein, as an experimental model. Most significantly, native Cd–Cup1 complexes were purified and fully spectroscopically and spectrometrically characterized from the 301N mutant yeast strain, which allows Cup1 synthesis even in the absence of copper. These results undoubtedly revealed the presence of a Cd– S2–Cup1 species in native preparations, which were only recovered when carefully avoiding the use of ion-exchange chromatography in the purification protocol. Furthermore, complete analysis of recombinant (Escherichia coli) Zn–Cup1, Cd–Cup1, and Cu– Cup1 and those complexes that result from Zn/Cd and Zn/Cu replacements in vitro and acidification/renaturalization processes yielded a comprehensive and comparative overview of the metal-binding abilities of Cup1. Overall, we consider the main conclusions of this study to go beyond the mere study of the particular Cup1 MT, so that they should be considered to delineate a new point of view on the interaction between copper-thioneins and divalent metal ions, still an unexplored aspect in MT research.
Fil: Orihuela, Rubén. Universitat Autonoma de Barcelona; España
Fil: Monteiro, Freddy. Universidad de Barcelona; España
Fil: Pagani, María Ayelén. Universidad de Barcelona; España. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Centro de Estudios Fotosintéticos y Bioquímicos (i); Argentina. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas; Argentina
Fil: Capdevila, Merce. Universitat Autonoma de Barcelona; España
Fil: Atrian, Silvia. Universidad de Barcelona; España
Materia
Bioinorganic Chemistry
Circular Dichroism
Metalloproteins
Metallothioneins
Sulfide Ligands
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/15375

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spelling Evidence of native Metal–S2–Metallothionein complexes confirmed by the analysis of Cup1 Divalent-Metal-Ion binding propertiesOrihuela, RubénMonteiro, FreddyPagani, María AyelénCapdevila, MerceAtrian, SilviaBioinorganic ChemistryCircular DichroismMetalloproteinsMetallothioneinsSulfide Ligandshttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1https://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1It has previously been shown that recombinant synthesis, under metal-supplemented conditions, of diverse metallothioneins (MTs) results in the recovery of a subpopulation of S2- containing complexes in addition to the S2-devoid canonical metal–MT species. Further significance of this finding has remained veiled by the possibility of it being a mere consequence of synthesis in a heterologous bacterial system. Herein, we present definitive evidence that S2 ligands are also constituents of native metal–MT complexes. Because, although practically universal, the highest S2 content is incorporated by copper-thioneins when coordinating divalent metal ions, we adapted the Saccharomyces cerevisiae Cup1 protein, which is the most paradigmatic copper-thionein, as an experimental model. Most significantly, native Cd–Cup1 complexes were purified and fully spectroscopically and spectrometrically characterized from the 301N mutant yeast strain, which allows Cup1 synthesis even in the absence of copper. These results undoubtedly revealed the presence of a Cd– S2–Cup1 species in native preparations, which were only recovered when carefully avoiding the use of ion-exchange chromatography in the purification protocol. Furthermore, complete analysis of recombinant (Escherichia coli) Zn–Cup1, Cd–Cup1, and Cu– Cup1 and those complexes that result from Zn/Cd and Zn/Cu replacements in vitro and acidification/renaturalization processes yielded a comprehensive and comparative overview of the metal-binding abilities of Cup1. Overall, we consider the main conclusions of this study to go beyond the mere study of the particular Cup1 MT, so that they should be considered to delineate a new point of view on the interaction between copper-thioneins and divalent metal ions, still an unexplored aspect in MT research.Fil: Orihuela, Rubén. Universitat Autonoma de Barcelona; EspañaFil: Monteiro, Freddy. Universidad de Barcelona; EspañaFil: Pagani, María Ayelén. Universidad de Barcelona; España. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Centro de Estudios Fotosintéticos y Bioquímicos (i); Argentina. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas; ArgentinaFil: Capdevila, Merce. Universitat Autonoma de Barcelona; EspañaFil: Atrian, Silvia. Universidad de Barcelona; EspañaWiley VCH Verlag2010-11info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/15375Orihuela, Rubén; Monteiro, Freddy; Pagani, María Ayelén; Capdevila, Merce; Atrian, Silvia; Evidence of native Metal–S2–Metallothionein complexes confirmed by the analysis of Cup1 Divalent-Metal-Ion binding properties; Wiley VCH Verlag; Chemistry- A European Journal; 16; 41; 11-2010; 12363-123721521-3765enginfo:eu-repo/semantics/altIdentifier/doi/10.1002/chem.201001125info:eu-repo/semantics/altIdentifier/url/http://onlinelibrary.wiley.com/doi/10.1002/chem.201001125/abstractinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T10:10:26Zoai:ri.conicet.gov.ar:11336/15375instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-29 10:10:27.242CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Evidence of native Metal–S2–Metallothionein complexes confirmed by the analysis of Cup1 Divalent-Metal-Ion binding properties
title Evidence of native Metal–S2–Metallothionein complexes confirmed by the analysis of Cup1 Divalent-Metal-Ion binding properties
spellingShingle Evidence of native Metal–S2–Metallothionein complexes confirmed by the analysis of Cup1 Divalent-Metal-Ion binding properties
Orihuela, Rubén
Bioinorganic Chemistry
Circular Dichroism
Metalloproteins
Metallothioneins
Sulfide Ligands
title_short Evidence of native Metal–S2–Metallothionein complexes confirmed by the analysis of Cup1 Divalent-Metal-Ion binding properties
title_full Evidence of native Metal–S2–Metallothionein complexes confirmed by the analysis of Cup1 Divalent-Metal-Ion binding properties
title_fullStr Evidence of native Metal–S2–Metallothionein complexes confirmed by the analysis of Cup1 Divalent-Metal-Ion binding properties
title_full_unstemmed Evidence of native Metal–S2–Metallothionein complexes confirmed by the analysis of Cup1 Divalent-Metal-Ion binding properties
title_sort Evidence of native Metal–S2–Metallothionein complexes confirmed by the analysis of Cup1 Divalent-Metal-Ion binding properties
dc.creator.none.fl_str_mv Orihuela, Rubén
Monteiro, Freddy
Pagani, María Ayelén
Capdevila, Merce
Atrian, Silvia
author Orihuela, Rubén
author_facet Orihuela, Rubén
Monteiro, Freddy
Pagani, María Ayelén
Capdevila, Merce
Atrian, Silvia
author_role author
author2 Monteiro, Freddy
Pagani, María Ayelén
Capdevila, Merce
Atrian, Silvia
author2_role author
author
author
author
dc.subject.none.fl_str_mv Bioinorganic Chemistry
Circular Dichroism
Metalloproteins
Metallothioneins
Sulfide Ligands
topic Bioinorganic Chemistry
Circular Dichroism
Metalloproteins
Metallothioneins
Sulfide Ligands
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv It has previously been shown that recombinant synthesis, under metal-supplemented conditions, of diverse metallothioneins (MTs) results in the recovery of a subpopulation of S2- containing complexes in addition to the S2-devoid canonical metal–MT species. Further significance of this finding has remained veiled by the possibility of it being a mere consequence of synthesis in a heterologous bacterial system. Herein, we present definitive evidence that S2 ligands are also constituents of native metal–MT complexes. Because, although practically universal, the highest S2 content is incorporated by copper-thioneins when coordinating divalent metal ions, we adapted the Saccharomyces cerevisiae Cup1 protein, which is the most paradigmatic copper-thionein, as an experimental model. Most significantly, native Cd–Cup1 complexes were purified and fully spectroscopically and spectrometrically characterized from the 301N mutant yeast strain, which allows Cup1 synthesis even in the absence of copper. These results undoubtedly revealed the presence of a Cd– S2–Cup1 species in native preparations, which were only recovered when carefully avoiding the use of ion-exchange chromatography in the purification protocol. Furthermore, complete analysis of recombinant (Escherichia coli) Zn–Cup1, Cd–Cup1, and Cu– Cup1 and those complexes that result from Zn/Cd and Zn/Cu replacements in vitro and acidification/renaturalization processes yielded a comprehensive and comparative overview of the metal-binding abilities of Cup1. Overall, we consider the main conclusions of this study to go beyond the mere study of the particular Cup1 MT, so that they should be considered to delineate a new point of view on the interaction between copper-thioneins and divalent metal ions, still an unexplored aspect in MT research.
Fil: Orihuela, Rubén. Universitat Autonoma de Barcelona; España
Fil: Monteiro, Freddy. Universidad de Barcelona; España
Fil: Pagani, María Ayelén. Universidad de Barcelona; España. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Rosario. Centro de Estudios Fotosintéticos y Bioquímicos (i); Argentina. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas; Argentina
Fil: Capdevila, Merce. Universitat Autonoma de Barcelona; España
Fil: Atrian, Silvia. Universidad de Barcelona; España
description It has previously been shown that recombinant synthesis, under metal-supplemented conditions, of diverse metallothioneins (MTs) results in the recovery of a subpopulation of S2- containing complexes in addition to the S2-devoid canonical metal–MT species. Further significance of this finding has remained veiled by the possibility of it being a mere consequence of synthesis in a heterologous bacterial system. Herein, we present definitive evidence that S2 ligands are also constituents of native metal–MT complexes. Because, although practically universal, the highest S2 content is incorporated by copper-thioneins when coordinating divalent metal ions, we adapted the Saccharomyces cerevisiae Cup1 protein, which is the most paradigmatic copper-thionein, as an experimental model. Most significantly, native Cd–Cup1 complexes were purified and fully spectroscopically and spectrometrically characterized from the 301N mutant yeast strain, which allows Cup1 synthesis even in the absence of copper. These results undoubtedly revealed the presence of a Cd– S2–Cup1 species in native preparations, which were only recovered when carefully avoiding the use of ion-exchange chromatography in the purification protocol. Furthermore, complete analysis of recombinant (Escherichia coli) Zn–Cup1, Cd–Cup1, and Cu– Cup1 and those complexes that result from Zn/Cd and Zn/Cu replacements in vitro and acidification/renaturalization processes yielded a comprehensive and comparative overview of the metal-binding abilities of Cup1. Overall, we consider the main conclusions of this study to go beyond the mere study of the particular Cup1 MT, so that they should be considered to delineate a new point of view on the interaction between copper-thioneins and divalent metal ions, still an unexplored aspect in MT research.
publishDate 2010
dc.date.none.fl_str_mv 2010-11
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/15375
Orihuela, Rubén; Monteiro, Freddy; Pagani, María Ayelén; Capdevila, Merce; Atrian, Silvia; Evidence of native Metal–S2–Metallothionein complexes confirmed by the analysis of Cup1 Divalent-Metal-Ion binding properties; Wiley VCH Verlag; Chemistry- A European Journal; 16; 41; 11-2010; 12363-12372
1521-3765
url http://hdl.handle.net/11336/15375
identifier_str_mv Orihuela, Rubén; Monteiro, Freddy; Pagani, María Ayelén; Capdevila, Merce; Atrian, Silvia; Evidence of native Metal–S2–Metallothionein complexes confirmed by the analysis of Cup1 Divalent-Metal-Ion binding properties; Wiley VCH Verlag; Chemistry- A European Journal; 16; 41; 11-2010; 12363-12372
1521-3765
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/doi/10.1002/chem.201001125
info:eu-repo/semantics/altIdentifier/url/http://onlinelibrary.wiley.com/doi/10.1002/chem.201001125/abstract
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Wiley VCH Verlag
publisher.none.fl_str_mv Wiley VCH Verlag
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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