Docking and electron transfer studies between rubredoxin and rubredoxin : oxygen oxidoreductase

Bibliographic Details
Main Author: Victor, Bruno
Publication Date: 2003
Other Authors: Vicente, João, Rodrigues, Rute, Oliveira, Solange, Rodrigues-Pousada, Claudina, Frazão, Carlos, Gomes, Cláudio, Teixeira, Miguel, Soares, Cláudio
Format: Article
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: http://hdl.handle.net/10174/2103
Summary: Abstract: The interaction and electron transfer (ET) between rubredoxin (Rd) and rubredoxin: oxygen oxidoreductase (ROO) from Desulfovibrio gigas is studied by molecular modelling techniques. Experimental kinetic assays using recombinant proteins show that the Rd reoxidation by ROO displays a bell-shaped dependence on ionic strength, suggesting a non-trivial electrostatic dependence of the interaction between these two proteins. Rigid docking studies reveal a prevalence for Rd to interact, in a very specific way, with the surface of the ROO dimer near its FMN cofactors. The optimization of the lowest energy complexes, using molecular dynamics simulation, shows a very tight interaction between the surface of the two proteins, with a high probability for Rd residues (but not the iron centre directly) to be in direct contact with the FMN cofactors of ROO. Both electrostatics and van der Waals interactions contribute to the final energy of the complex. In these complexes, the major contributions for complex formation are polar interactions between acidic residues of Rd and basic residues of ROO, plus substantial non-polar interactions between different groups. Important residues for this process are identified. ET estimates (using the Pathways model), in the optimized lowest energy complexes, suggest that these configurations are efficient for transferring electrons. The experimental bell-shaped dependence of kinetics on ionic strength is analysed in view of the molecular modelling results, and hypotheses for the molecular basis of this phenomenon are discussed.
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spelling Docking and electron transfer studies between rubredoxin and rubredoxin : oxygen oxidoreductaserubredoxinROOAbstract: The interaction and electron transfer (ET) between rubredoxin (Rd) and rubredoxin: oxygen oxidoreductase (ROO) from Desulfovibrio gigas is studied by molecular modelling techniques. Experimental kinetic assays using recombinant proteins show that the Rd reoxidation by ROO displays a bell-shaped dependence on ionic strength, suggesting a non-trivial electrostatic dependence of the interaction between these two proteins. Rigid docking studies reveal a prevalence for Rd to interact, in a very specific way, with the surface of the ROO dimer near its FMN cofactors. The optimization of the lowest energy complexes, using molecular dynamics simulation, shows a very tight interaction between the surface of the two proteins, with a high probability for Rd residues (but not the iron centre directly) to be in direct contact with the FMN cofactors of ROO. Both electrostatics and van der Waals interactions contribute to the final energy of the complex. In these complexes, the major contributions for complex formation are polar interactions between acidic residues of Rd and basic residues of ROO, plus substantial non-polar interactions between different groups. Important residues for this process are identified. ET estimates (using the Pathways model), in the optimized lowest energy complexes, suggest that these configurations are efficient for transferring electrons. The experimental bell-shaped dependence of kinetics on ionic strength is analysed in view of the molecular modelling results, and hypotheses for the molecular basis of this phenomenon are discussed.2010-09-27T14:44:17Z2010-09-272003-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article126583 bytesapplication/pdfhttp://hdl.handle.net/10174/2103http://hdl.handle.net/10174/2103engpag 475-4888JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRYlivrendndndndndndndndnd548Victor, BrunoVicente, JoãoRodrigues, RuteOliveira, SolangeRodrigues-Pousada, ClaudinaFrazão, CarlosGomes, CláudioTeixeira, MiguelSoares, Cláudioinfo:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2024-01-03T18:38:17Zoai:dspace.uevora.pt:10174/2103Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T11:50:59.264093Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Docking and electron transfer studies between rubredoxin and rubredoxin : oxygen oxidoreductase
title Docking and electron transfer studies between rubredoxin and rubredoxin : oxygen oxidoreductase
spellingShingle Docking and electron transfer studies between rubredoxin and rubredoxin : oxygen oxidoreductase
Victor, Bruno
rubredoxin
ROO
title_short Docking and electron transfer studies between rubredoxin and rubredoxin : oxygen oxidoreductase
title_full Docking and electron transfer studies between rubredoxin and rubredoxin : oxygen oxidoreductase
title_fullStr Docking and electron transfer studies between rubredoxin and rubredoxin : oxygen oxidoreductase
title_full_unstemmed Docking and electron transfer studies between rubredoxin and rubredoxin : oxygen oxidoreductase
title_sort Docking and electron transfer studies between rubredoxin and rubredoxin : oxygen oxidoreductase
author Victor, Bruno
author_facet Victor, Bruno
Vicente, João
Rodrigues, Rute
Oliveira, Solange
Rodrigues-Pousada, Claudina
Frazão, Carlos
Gomes, Cláudio
Teixeira, Miguel
Soares, Cláudio
author_role author
author2 Vicente, João
Rodrigues, Rute
Oliveira, Solange
Rodrigues-Pousada, Claudina
Frazão, Carlos
Gomes, Cláudio
Teixeira, Miguel
Soares, Cláudio
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Victor, Bruno
Vicente, João
Rodrigues, Rute
Oliveira, Solange
Rodrigues-Pousada, Claudina
Frazão, Carlos
Gomes, Cláudio
Teixeira, Miguel
Soares, Cláudio
dc.subject.por.fl_str_mv rubredoxin
ROO
topic rubredoxin
ROO
description Abstract: The interaction and electron transfer (ET) between rubredoxin (Rd) and rubredoxin: oxygen oxidoreductase (ROO) from Desulfovibrio gigas is studied by molecular modelling techniques. Experimental kinetic assays using recombinant proteins show that the Rd reoxidation by ROO displays a bell-shaped dependence on ionic strength, suggesting a non-trivial electrostatic dependence of the interaction between these two proteins. Rigid docking studies reveal a prevalence for Rd to interact, in a very specific way, with the surface of the ROO dimer near its FMN cofactors. The optimization of the lowest energy complexes, using molecular dynamics simulation, shows a very tight interaction between the surface of the two proteins, with a high probability for Rd residues (but not the iron centre directly) to be in direct contact with the FMN cofactors of ROO. Both electrostatics and van der Waals interactions contribute to the final energy of the complex. In these complexes, the major contributions for complex formation are polar interactions between acidic residues of Rd and basic residues of ROO, plus substantial non-polar interactions between different groups. Important residues for this process are identified. ET estimates (using the Pathways model), in the optimized lowest energy complexes, suggest that these configurations are efficient for transferring electrons. The experimental bell-shaped dependence of kinetics on ionic strength is analysed in view of the molecular modelling results, and hypotheses for the molecular basis of this phenomenon are discussed.
publishDate 2003
dc.date.none.fl_str_mv 2003-01-01T00:00:00Z
2010-09-27T14:44:17Z
2010-09-27
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