Metallomics-based platforms for comparing the human blood serum profiles between bipolar disorder and schizophrenia patients

Detalhes bibliográficos
Autor(a) principal: Souza Pessoa, Gustavo de
Data de Publicação: 2020
Outros Autores: Jesus, Jemmyson Romario de, Balbuena, Tiago Santana [UNESP], Arruda, Marco Aurelio Zezzi
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1002/rcm.8698
http://hdl.handle.net/11449/196583
Resumo: Rationale An evaluation of bipolar disorder (BD) and schizophrenia (SCZ) was carried out, from a metallomics point of view, using native conditions, attempting to preserve the interaction between metals and biomolecules. Method For this task, blood serum samples from healthy individuals and patients were compared. In addition, the profiles of metal ions and metalloids involved in the pathologies were quantified, and a comparison was carried out of the protein profile in serum samples of healthy individuals and diseased patients. Results After optimization and accuracy evaluation of the method, different concentrations of Li, Mg, Mn and Zn were observed in the samples of BD patients and high levels of copper for SCZ patients, indicating an imbalance in the homeostasis of important micronutrients. The treatment, especially with lithium, may be related to competition between metallic ions. BD-related metallobiomolecules were detected, preserving the binding between metal ions and biomolecules, with four fractions detected in the ultraviolet range (280 nm). Four fractions were collected by high-performance liquid chromatography/inductively coupled plasma mass spectrometry (HPLC/ICP-MS) and the proteins were identified by liquid chromatography/tandem mass spectrometry (LC/MS/MS). The Ig lambda chain V-IV region Hil, immunoglobulin heavy constant gama 1 (IGHG1) and beta-2-glycoprotein 1 (or ApoH) was identified in SCZ samples, suggesting its relationship with mood disorders. Surprisingly, Protein IGKV2D-28 was identified only in BD samples, opening up new possibilities for studies regarding the role of this protein in BD. Conclusions This approach brings new perspectives to the comprehension of mood disorders, highlighting the importance of metallomics science in disease development. This strategy showed an innovative potential for evaluating mood disorders at the proteomic level, making it possible to identify proteins related to mood disorders and BD.
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spelling Metallomics-based platforms for comparing the human blood serum profiles between bipolar disorder and schizophrenia patientsRationale An evaluation of bipolar disorder (BD) and schizophrenia (SCZ) was carried out, from a metallomics point of view, using native conditions, attempting to preserve the interaction between metals and biomolecules. Method For this task, blood serum samples from healthy individuals and patients were compared. In addition, the profiles of metal ions and metalloids involved in the pathologies were quantified, and a comparison was carried out of the protein profile in serum samples of healthy individuals and diseased patients. Results After optimization and accuracy evaluation of the method, different concentrations of Li, Mg, Mn and Zn were observed in the samples of BD patients and high levels of copper for SCZ patients, indicating an imbalance in the homeostasis of important micronutrients. The treatment, especially with lithium, may be related to competition between metallic ions. BD-related metallobiomolecules were detected, preserving the binding between metal ions and biomolecules, with four fractions detected in the ultraviolet range (280 nm). Four fractions were collected by high-performance liquid chromatography/inductively coupled plasma mass spectrometry (HPLC/ICP-MS) and the proteins were identified by liquid chromatography/tandem mass spectrometry (LC/MS/MS). The Ig lambda chain V-IV region Hil, immunoglobulin heavy constant gama 1 (IGHG1) and beta-2-glycoprotein 1 (or ApoH) was identified in SCZ samples, suggesting its relationship with mood disorders. Surprisingly, Protein IGKV2D-28 was identified only in BD samples, opening up new possibilities for studies regarding the role of this protein in BD. Conclusions This approach brings new perspectives to the comprehension of mood disorders, highlighting the importance of metallomics science in disease development. This strategy showed an innovative potential for evaluating mood disorders at the proteomic level, making it possible to identify proteins related to mood disorders and BD.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Univ Estadual Campinas, UNICAMP, Inst Chem, Grp Spectrometry Sample Preparat & Mechanizat GEP, POB 6154, BR-13084862 Campinas, SP, BrazilUniv Estadual Campinas, UNICAMP, Inst Chem, Natl Inst Sci & Technol Bioanalyt, BR-13084862 Campinas, SP, BrazilUniv Estadual Paulista, Fac Ciencias Agr & Vet, Dept Tecnol, Jaboticabal, SP, BrazilUniv Estadual Paulista, Fac Ciencias Agr & Vet, Dept Tecnol, Jaboticabal, SP, BrazilCAPES: 88887.115406/2015FAPESP: 2014/50867-3FAPESP: 2016/07384-7FAPESP: 2018/25207-0Wiley-BlackwellUniversidade Estadual de Campinas (UNICAMP)Universidade Estadual Paulista (Unesp)Souza Pessoa, Gustavo deJesus, Jemmyson Romario deBalbuena, Tiago Santana [UNESP]Arruda, Marco Aurelio Zezzi2020-12-10T19:49:33Z2020-12-10T19:49:33Z2020-02-18info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article10http://dx.doi.org/10.1002/rcm.8698Rapid Communications In Mass Spectrometry. Hoboken: Wiley, 10 p., 2020.0951-4198http://hdl.handle.net/11449/19658310.1002/rcm.8698WOS:000514009700001Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengRapid Communications In Mass Spectrometryinfo:eu-repo/semantics/openAccess2024-06-07T15:32:11Zoai:repositorio.unesp.br:11449/196583Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T19:46:20.588009Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Metallomics-based platforms for comparing the human blood serum profiles between bipolar disorder and schizophrenia patients
title Metallomics-based platforms for comparing the human blood serum profiles between bipolar disorder and schizophrenia patients
spellingShingle Metallomics-based platforms for comparing the human blood serum profiles between bipolar disorder and schizophrenia patients
Souza Pessoa, Gustavo de
title_short Metallomics-based platforms for comparing the human blood serum profiles between bipolar disorder and schizophrenia patients
title_full Metallomics-based platforms for comparing the human blood serum profiles between bipolar disorder and schizophrenia patients
title_fullStr Metallomics-based platforms for comparing the human blood serum profiles between bipolar disorder and schizophrenia patients
title_full_unstemmed Metallomics-based platforms for comparing the human blood serum profiles between bipolar disorder and schizophrenia patients
title_sort Metallomics-based platforms for comparing the human blood serum profiles between bipolar disorder and schizophrenia patients
author Souza Pessoa, Gustavo de
author_facet Souza Pessoa, Gustavo de
Jesus, Jemmyson Romario de
Balbuena, Tiago Santana [UNESP]
Arruda, Marco Aurelio Zezzi
author_role author
author2 Jesus, Jemmyson Romario de
Balbuena, Tiago Santana [UNESP]
Arruda, Marco Aurelio Zezzi
author2_role author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual de Campinas (UNICAMP)
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Souza Pessoa, Gustavo de
Jesus, Jemmyson Romario de
Balbuena, Tiago Santana [UNESP]
Arruda, Marco Aurelio Zezzi
description Rationale An evaluation of bipolar disorder (BD) and schizophrenia (SCZ) was carried out, from a metallomics point of view, using native conditions, attempting to preserve the interaction between metals and biomolecules. Method For this task, blood serum samples from healthy individuals and patients were compared. In addition, the profiles of metal ions and metalloids involved in the pathologies were quantified, and a comparison was carried out of the protein profile in serum samples of healthy individuals and diseased patients. Results After optimization and accuracy evaluation of the method, different concentrations of Li, Mg, Mn and Zn were observed in the samples of BD patients and high levels of copper for SCZ patients, indicating an imbalance in the homeostasis of important micronutrients. The treatment, especially with lithium, may be related to competition between metallic ions. BD-related metallobiomolecules were detected, preserving the binding between metal ions and biomolecules, with four fractions detected in the ultraviolet range (280 nm). Four fractions were collected by high-performance liquid chromatography/inductively coupled plasma mass spectrometry (HPLC/ICP-MS) and the proteins were identified by liquid chromatography/tandem mass spectrometry (LC/MS/MS). The Ig lambda chain V-IV region Hil, immunoglobulin heavy constant gama 1 (IGHG1) and beta-2-glycoprotein 1 (or ApoH) was identified in SCZ samples, suggesting its relationship with mood disorders. Surprisingly, Protein IGKV2D-28 was identified only in BD samples, opening up new possibilities for studies regarding the role of this protein in BD. Conclusions This approach brings new perspectives to the comprehension of mood disorders, highlighting the importance of metallomics science in disease development. This strategy showed an innovative potential for evaluating mood disorders at the proteomic level, making it possible to identify proteins related to mood disorders and BD.
publishDate 2020
dc.date.none.fl_str_mv 2020-12-10T19:49:33Z
2020-12-10T19:49:33Z
2020-02-18
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://dx.doi.org/10.1002/rcm.8698
Rapid Communications In Mass Spectrometry. Hoboken: Wiley, 10 p., 2020.
0951-4198
http://hdl.handle.net/11449/196583
10.1002/rcm.8698
WOS:000514009700001
url http://dx.doi.org/10.1002/rcm.8698
http://hdl.handle.net/11449/196583
identifier_str_mv Rapid Communications In Mass Spectrometry. Hoboken: Wiley, 10 p., 2020.
0951-4198
10.1002/rcm.8698
WOS:000514009700001
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Rapid Communications In Mass Spectrometry
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 10
dc.publisher.none.fl_str_mv Wiley-Blackwell
publisher.none.fl_str_mv Wiley-Blackwell
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
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