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
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/15375
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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 |
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CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
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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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1844613994209345536 |
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13.070432 |