Zinc-substituted desulfovibrio gigas desulforedoxins
Autor(a) principal: | |
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Data de Publicação: | 2002 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10362/1655 |
Resumo: | Protein Science (2002), 11:2464–2470 |
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Zinc-substituted desulfovibrio gigas desulforedoxinsResolving subunit degeneracy with nonsymmetric pseudocontact shiftsNMRPseudocontact shiftsDesulforedoxin[Fe-4S] centerParamagnetic proteinDesulfovibrio gigasProtein Science (2002), 11:2464–2470Desulfovibrio gigas desulforedoxin (Dx) consists of two identical peptides, each containing one [Fe-4S]center per monomer. Variants with different iron and zinc metal compositions arise when desulforedoxin is produced recombinantly from Escherichia coli. The three forms of the protein, the two homodimers [Fe(III)/Fe(III)]Dx and [Zn(II)/Zn(II)]Dx, and the heterodimer [Fe(III)/Zn(II)]Dx, can be separated by ion exchange chromatography on the basis of their charge differences. Once separated, the desulforedoxins containing iron can be reduced with added dithionite. For NMR studies, different protein samples were prepared labeled with 15N or 15N + 13C. Spectral assignments were determined for [Fe(II)/Fe(II)]Dx and [Fe(II)/Zn(II)]Dx from 3D 15N TOCSY-HSQC and NOESY-HSQC data, and compared with those reported previously for [Zn(II)/Zn(II)]Dx. Assignments for the 13C shifts were obtained from an HNCA experiment. Comparison of 1H–15N HSQC spectra of [Zn(II)/Zn(II)]Dx, [Fe(II)/Fe(II)]Dx and [Fe(II)/Zn(II)]Dx revealed that the pseudocontact shifts in [Fe(II)/Zn(II)]Dx can be decomposed into inter- and intramonomer components, which, when summed, accurately predict the observed pseudocontact shifts observed for [Fe(II)/Fe(II)]Dx. The degree of linearity observed in the pseudocontact shifts for residues 8.5 Å from the metal center indicates that the replacement of Fe(II) by Zn(II) produces little or no change in the structure of Dx. The results suggest a general strategy for the analysis of NMR spectra of homo-oligomeric proteins in which a paramagnetic center introduced into a single subunit is used to break the magnetic symmetry and make it possible to obtain distance constraints (both pseudocontact and NOE) between subunits.Cold Spring Harbor Laboratory PressRUNMoura, IsabelGoodfellow, Brian J.Nunes, Sofia G.Rusnak, FrankAscenso, CarlaMoura, José J. G.Volkman, Brian F.Markley, John L.2008-09-23T13:06:21Z20022002-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10362/1655enginfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-03-11T03:31:38Zoai:run.unl.pt:10362/1655Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T03:14:46.849158Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Zinc-substituted desulfovibrio gigas desulforedoxins Resolving subunit degeneracy with nonsymmetric pseudocontact shifts |
title |
Zinc-substituted desulfovibrio gigas desulforedoxins |
spellingShingle |
Zinc-substituted desulfovibrio gigas desulforedoxins Moura, Isabel NMR Pseudocontact shifts Desulforedoxin [Fe-4S] center Paramagnetic protein Desulfovibrio gigas |
title_short |
Zinc-substituted desulfovibrio gigas desulforedoxins |
title_full |
Zinc-substituted desulfovibrio gigas desulforedoxins |
title_fullStr |
Zinc-substituted desulfovibrio gigas desulforedoxins |
title_full_unstemmed |
Zinc-substituted desulfovibrio gigas desulforedoxins |
title_sort |
Zinc-substituted desulfovibrio gigas desulforedoxins |
author |
Moura, Isabel |
author_facet |
Moura, Isabel Goodfellow, Brian J. Nunes, Sofia G. Rusnak, Frank Ascenso, Carla Moura, José J. G. Volkman, Brian F. Markley, John L. |
author_role |
author |
author2 |
Goodfellow, Brian J. Nunes, Sofia G. Rusnak, Frank Ascenso, Carla Moura, José J. G. Volkman, Brian F. Markley, John L. |
author2_role |
author author author author author author author |
dc.contributor.none.fl_str_mv |
RUN |
dc.contributor.author.fl_str_mv |
Moura, Isabel Goodfellow, Brian J. Nunes, Sofia G. Rusnak, Frank Ascenso, Carla Moura, José J. G. Volkman, Brian F. Markley, John L. |
dc.subject.por.fl_str_mv |
NMR Pseudocontact shifts Desulforedoxin [Fe-4S] center Paramagnetic protein Desulfovibrio gigas |
topic |
NMR Pseudocontact shifts Desulforedoxin [Fe-4S] center Paramagnetic protein Desulfovibrio gigas |
description |
Protein Science (2002), 11:2464–2470 |
publishDate |
2002 |
dc.date.none.fl_str_mv |
2002 2002-01-01T00:00:00Z 2008-09-23T13:06:21Z |
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.uri.fl_str_mv |
http://hdl.handle.net/10362/1655 |
url |
http://hdl.handle.net/10362/1655 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Cold Spring Harbor Laboratory Press |
publisher.none.fl_str_mv |
Cold Spring Harbor Laboratory Press |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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1799137800299216896 |