Metallomics-based platforms for comparing the human blood serum profiles between bipolar disorder and schizophrenia patients
Autor(a) principal: | |
---|---|
Data de Publicação: | 2020 |
Outros Autores: | , , |
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. |
id |
UNSP_c300099490cba29435a75097adeb3b57 |
---|---|
oai_identifier_str |
oai:repositorio.unesp.br:11449/196583 |
network_acronym_str |
UNSP |
network_name_str |
Repositório Institucional da UNESP |
repository_id_str |
2946 |
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) |
repository.mail.fl_str_mv |
|
_version_ |
1808129116625436672 |