Investigation of interaction of nuclear fast red with human serum albumin by experimental and computational approaches

Autores
Gholivanda, Mohammad Bagher; Jalalvand, Ali R.; Goicoechea, Hector Casimiro; Omidi, Mehdi
Año de publicación
2013
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
For the first time, interaction of nuclear fast red (NFR) with human serum albumin (HSA) was studied by experimental and computational approaches. Firstly, experimental measurements including fluorescence spectroscopy (F), UVvis spectrophotometry (UVvis), cyclic voltammetry (CV), differential pulse voltammetry (DPV) and linear sweep voltammetry (LSV) were separately used to investigate the interaction of NFR with HSA and interesting thermodynamics information was obtained from these studies. Secondly, new information including electrochemical behavior of NFR–HSA complex species, relative concentrations of the various reacting species and effects of NFR on the sub-structure of HSA was obtained by applying multivariate curve resolution–alternating least squares (MCR–ALS). In this case, a row- and column-wise augmented matrix was built with DPV, LSV, F and UVvis sub-matrices and resolved by MCR–ALS. Surprisingly, by this method two NFR–HSA complex species with different stoichiometries and different electrochemical behaviors were found. Furthermore, by the use of the recorded voltammetric and spectroscopic data the binding constants of complex species were computed by EQUISPEC (a hard-modeling algorithm). Finally, the binding of NFR to HSA was modeled by molecular modeling and molecular dynamics (MD) simulations methods. Excellent agreement was found between experimental and computational results. Both experimental and computational results suggested that the NFR binds mainly to the sub-domain IIA of HSA.
Fil: Gholivanda, Mohammad Bagher. Razi University. Faculty of Chemistry. Department of Analytical Chemistry; Irán
Fil: Jalalvand, Ali R.. Razi University. Faculty of Chemistry. Department of Analytical Chemistry; Irán. Kermanshah Oil Refining Company. Quality Control Laboratory; Irán
Fil: Goicoechea, Hector Casimiro. Universidad Nacional del Litoral. Facultad de Ingenieria Quimica. Laboratorio de Quimica Analitica; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Santa Fe; Argentina
Fil: Omidi, Mehdi. Razi University. Faculty of Chemistry. Department of Analytical Chemistry; Irán
Materia
Nuclear Fast Red
Voltametry
Spectroscopy
Computational Aproaches
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/6409

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spelling Investigation of interaction of nuclear fast red with human serum albumin by experimental and computational approachesGholivanda, Mohammad BagherJalalvand, Ali R.Goicoechea, Hector CasimiroOmidi, MehdiNuclear Fast RedVoltametrySpectroscopyComputational Aproacheshttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1For the first time, interaction of nuclear fast red (NFR) with human serum albumin (HSA) was studied by experimental and computational approaches. Firstly, experimental measurements including fluorescence spectroscopy (F), UVvis spectrophotometry (UVvis), cyclic voltammetry (CV), differential pulse voltammetry (DPV) and linear sweep voltammetry (LSV) were separately used to investigate the interaction of NFR with HSA and interesting thermodynamics information was obtained from these studies. Secondly, new information including electrochemical behavior of NFR–HSA complex species, relative concentrations of the various reacting species and effects of NFR on the sub-structure of HSA was obtained by applying multivariate curve resolution–alternating least squares (MCR–ALS). In this case, a row- and column-wise augmented matrix was built with DPV, LSV, F and UVvis sub-matrices and resolved by MCR–ALS. Surprisingly, by this method two NFR–HSA complex species with different stoichiometries and different electrochemical behaviors were found. Furthermore, by the use of the recorded voltammetric and spectroscopic data the binding constants of complex species were computed by EQUISPEC (a hard-modeling algorithm). Finally, the binding of NFR to HSA was modeled by molecular modeling and molecular dynamics (MD) simulations methods. Excellent agreement was found between experimental and computational results. Both experimental and computational results suggested that the NFR binds mainly to the sub-domain IIA of HSA.Fil: Gholivanda, Mohammad Bagher. Razi University. Faculty of Chemistry. Department of Analytical Chemistry; IránFil: Jalalvand, Ali R.. Razi University. Faculty of Chemistry. Department of Analytical Chemistry; Irán. Kermanshah Oil Refining Company. Quality Control Laboratory; IránFil: Goicoechea, Hector Casimiro. Universidad Nacional del Litoral. Facultad de Ingenieria Quimica. Laboratorio de Quimica Analitica; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Santa Fe; ArgentinaFil: Omidi, Mehdi. Razi University. Faculty of Chemistry. Department of Analytical Chemistry; IránElsevier2013-07info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/6409Gholivanda, Mohammad Bagher; Jalalvand, Ali R.; Goicoechea, Hector Casimiro; Omidi, Mehdi; Investigation of interaction of nuclear fast red with human serum albumin by experimental and computational approaches; Elsevier; Spectrochimica Acta A: Molecular and Biomolecular Spectroscopy; 115; 7-2013; 516-5271386-1425enginfo:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S1386142513006483info:eu-repo/semantics/altIdentifier/doi/10.1016/j.saa.2013.06.044info:eu-repo/semantics/altIdentifier/doi/info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-nd/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-15T14:31:18Zoai:ri.conicet.gov.ar:11336/6409instacron: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:34982025-10-15 14:31:18.372CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Investigation of interaction of nuclear fast red with human serum albumin by experimental and computational approaches
title Investigation of interaction of nuclear fast red with human serum albumin by experimental and computational approaches
spellingShingle Investigation of interaction of nuclear fast red with human serum albumin by experimental and computational approaches
Gholivanda, Mohammad Bagher
Nuclear Fast Red
Voltametry
Spectroscopy
Computational Aproaches
title_short Investigation of interaction of nuclear fast red with human serum albumin by experimental and computational approaches
title_full Investigation of interaction of nuclear fast red with human serum albumin by experimental and computational approaches
title_fullStr Investigation of interaction of nuclear fast red with human serum albumin by experimental and computational approaches
title_full_unstemmed Investigation of interaction of nuclear fast red with human serum albumin by experimental and computational approaches
title_sort Investigation of interaction of nuclear fast red with human serum albumin by experimental and computational approaches
dc.creator.none.fl_str_mv Gholivanda, Mohammad Bagher
Jalalvand, Ali R.
Goicoechea, Hector Casimiro
Omidi, Mehdi
author Gholivanda, Mohammad Bagher
author_facet Gholivanda, Mohammad Bagher
Jalalvand, Ali R.
Goicoechea, Hector Casimiro
Omidi, Mehdi
author_role author
author2 Jalalvand, Ali R.
Goicoechea, Hector Casimiro
Omidi, Mehdi
author2_role author
author
author
dc.subject.none.fl_str_mv Nuclear Fast Red
Voltametry
Spectroscopy
Computational Aproaches
topic Nuclear Fast Red
Voltametry
Spectroscopy
Computational Aproaches
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv For the first time, interaction of nuclear fast red (NFR) with human serum albumin (HSA) was studied by experimental and computational approaches. Firstly, experimental measurements including fluorescence spectroscopy (F), UVvis spectrophotometry (UVvis), cyclic voltammetry (CV), differential pulse voltammetry (DPV) and linear sweep voltammetry (LSV) were separately used to investigate the interaction of NFR with HSA and interesting thermodynamics information was obtained from these studies. Secondly, new information including electrochemical behavior of NFR–HSA complex species, relative concentrations of the various reacting species and effects of NFR on the sub-structure of HSA was obtained by applying multivariate curve resolution–alternating least squares (MCR–ALS). In this case, a row- and column-wise augmented matrix was built with DPV, LSV, F and UVvis sub-matrices and resolved by MCR–ALS. Surprisingly, by this method two NFR–HSA complex species with different stoichiometries and different electrochemical behaviors were found. Furthermore, by the use of the recorded voltammetric and spectroscopic data the binding constants of complex species were computed by EQUISPEC (a hard-modeling algorithm). Finally, the binding of NFR to HSA was modeled by molecular modeling and molecular dynamics (MD) simulations methods. Excellent agreement was found between experimental and computational results. Both experimental and computational results suggested that the NFR binds mainly to the sub-domain IIA of HSA.
Fil: Gholivanda, Mohammad Bagher. Razi University. Faculty of Chemistry. Department of Analytical Chemistry; Irán
Fil: Jalalvand, Ali R.. Razi University. Faculty of Chemistry. Department of Analytical Chemistry; Irán. Kermanshah Oil Refining Company. Quality Control Laboratory; Irán
Fil: Goicoechea, Hector Casimiro. Universidad Nacional del Litoral. Facultad de Ingenieria Quimica. Laboratorio de Quimica Analitica; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Santa Fe; Argentina
Fil: Omidi, Mehdi. Razi University. Faculty of Chemistry. Department of Analytical Chemistry; Irán
description For the first time, interaction of nuclear fast red (NFR) with human serum albumin (HSA) was studied by experimental and computational approaches. Firstly, experimental measurements including fluorescence spectroscopy (F), UVvis spectrophotometry (UVvis), cyclic voltammetry (CV), differential pulse voltammetry (DPV) and linear sweep voltammetry (LSV) were separately used to investigate the interaction of NFR with HSA and interesting thermodynamics information was obtained from these studies. Secondly, new information including electrochemical behavior of NFR–HSA complex species, relative concentrations of the various reacting species and effects of NFR on the sub-structure of HSA was obtained by applying multivariate curve resolution–alternating least squares (MCR–ALS). In this case, a row- and column-wise augmented matrix was built with DPV, LSV, F and UVvis sub-matrices and resolved by MCR–ALS. Surprisingly, by this method two NFR–HSA complex species with different stoichiometries and different electrochemical behaviors were found. Furthermore, by the use of the recorded voltammetric and spectroscopic data the binding constants of complex species were computed by EQUISPEC (a hard-modeling algorithm). Finally, the binding of NFR to HSA was modeled by molecular modeling and molecular dynamics (MD) simulations methods. Excellent agreement was found between experimental and computational results. Both experimental and computational results suggested that the NFR binds mainly to the sub-domain IIA of HSA.
publishDate 2013
dc.date.none.fl_str_mv 2013-07
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/11336/6409
Gholivanda, Mohammad Bagher; Jalalvand, Ali R.; Goicoechea, Hector Casimiro; Omidi, Mehdi; Investigation of interaction of nuclear fast red with human serum albumin by experimental and computational approaches; Elsevier; Spectrochimica Acta A: Molecular and Biomolecular Spectroscopy; 115; 7-2013; 516-527
1386-1425
url http://hdl.handle.net/11336/6409
identifier_str_mv Gholivanda, Mohammad Bagher; Jalalvand, Ali R.; Goicoechea, Hector Casimiro; Omidi, Mehdi; Investigation of interaction of nuclear fast red with human serum albumin by experimental and computational approaches; Elsevier; Spectrochimica Acta A: Molecular and Biomolecular Spectroscopy; 115; 7-2013; 516-527
1386-1425
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S1386142513006483
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.saa.2013.06.044
info:eu-repo/semantics/altIdentifier/doi/
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
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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