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
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/6409
Ver los metadatos del registro completo
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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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1846082795648057344 |
score |
13.22299 |