Increased chemical acetylation of peptides and proteins in rats after daily ingestion of diacetyl analyzed by Nano-LC-MS/MS

Detalhes bibliográficos
Autor(a) principal: Jedlicka, Leticia Dias Lima [UNIFESP]
Data de Publicação: 2018
Outros Autores: Guterres, Sheila Barreto [UNIFESP], Balbino, Aleksandro Martins [UNIFESP], Bruno Neto, Giuseppe [UNIFESP], Landgraf, Richardt Gama [UNIFESP], Fernandes, Liliam [UNIFESP], Carrilho, Emanuel, Bechara, Etelvino José Henriques [UNIFESP], Assunção, Nilson Antonio [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: https://repositorio.unifesp.br/handle/11600/55628
http://dx.doi.org/10.7717/peerj.4688
Resumo: Background. Acetylation alters several protein properties including molecular weight, stability, enzymatic activity, protein protein interactions, and other biological functions. Our previous findings demonstrating that diacetyl/peroxynitrite can acetylate L-lysine, L-histidine, and albumin in vitro led us to investigate whether diacetyl-treated rats suffer protein acetylation as well. Methods. Wistar rats were administered diacetyl daily for four weeks, after which they were sacrificed, and their lung proteins were extracted to be analysed by Nano-LC-MS/MS (Q-TOF). A C18 reversed-phase colurnn and gradient elution with formic acid/acetonitrile solutions from 2 to 50% over 150 min were used to separate the proteins. Protein detection was performed using a microTOE-Q II (QTOF) equipped with captive source and an electrospray-ionization source. The data frommass spectrometry were processed using a Compass 1.7 and analyzed using Protein Scape, software that uses Mascot algorithms to perform protein searches. Results. A set of 3,162 acetylated peptides derived from 351 acetylated proteins in the diacetyl-treated group was identified. Among them, 23 targeted proteins were significantly more acetylated in the diacetyl-treated group than in the PBS control. Protein acetylation of the group treated with 540 mg/kg/day of diacetyl was corroborated by Western blotting analysis. Conclusions. These data support our hypothesis that diacetyl exposure in animals may lead to the generation of acetyl radicals, compounds that attach to proteins, affecting their functions and triggering adverse health problems.
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spelling Jedlicka, Leticia Dias Lima [UNIFESP]Guterres, Sheila Barreto [UNIFESP]Balbino, Aleksandro Martins [UNIFESP]Bruno Neto, Giuseppe [UNIFESP]Landgraf, Richardt Gama [UNIFESP]Fernandes, Liliam [UNIFESP]Carrilho, EmanuelBechara, Etelvino José Henriques [UNIFESP]Assunção, Nilson Antonio [UNIFESP]2020-07-20T16:30:59Z2020-07-20T16:30:59Z2018Peerj. London, v. 6, p. -, 2018.2167-8359https://repositorio.unifesp.br/handle/11600/55628http://dx.doi.org/10.7717/peerj.4688WOS000430890200002.pdf10.7717/peerj.4688WOS:000430890200002Background. Acetylation alters several protein properties including molecular weight, stability, enzymatic activity, protein protein interactions, and other biological functions. Our previous findings demonstrating that diacetyl/peroxynitrite can acetylate L-lysine, L-histidine, and albumin in vitro led us to investigate whether diacetyl-treated rats suffer protein acetylation as well. Methods. Wistar rats were administered diacetyl daily for four weeks, after which they were sacrificed, and their lung proteins were extracted to be analysed by Nano-LC-MS/MS (Q-TOF). A C18 reversed-phase colurnn and gradient elution with formic acid/acetonitrile solutions from 2 to 50% over 150 min were used to separate the proteins. Protein detection was performed using a microTOE-Q II (QTOF) equipped with captive source and an electrospray-ionization source. The data frommass spectrometry were processed using a Compass 1.7 and analyzed using Protein Scape, software that uses Mascot algorithms to perform protein searches. Results. A set of 3,162 acetylated peptides derived from 351 acetylated proteins in the diacetyl-treated group was identified. Among them, 23 targeted proteins were significantly more acetylated in the diacetyl-treated group than in the PBS control. Protein acetylation of the group treated with 540 mg/kg/day of diacetyl was corroborated by Western blotting analysis. Conclusions. These data support our hypothesis that diacetyl exposure in animals may lead to the generation of acetyl radicals, compounds that attach to proteins, affecting their functions and triggering adverse health problems.Sao Paulo Research Foundation (FAPESP)Brazilian Innovation Agency (FINEP)Univ Fed Sao Paulo, Inst Environm Chem & Pharmaceut Sci, Diadema, SP, BrazilUniv Fed Sul & Sudeste Para, Inst Studies Hlth & Biol, Collect Hlth, Maraba, PA, BrazilFundacao Univ Fed Rondonia, Dept Chem, Porto Velho, RO, BrazilUniv Sao Paulo, Sao Carlos Inst Chem, Sao Carlos, SP, BrazilUniv Sao Paulo, Inst Chem, Dept Fundamental Chem, Sao Paulo, SP, BrazilUniv Fed Sao Paulo, Inst Environm Chem & Pharmaceut Sci, Diadema, SP, BrazilFAPESP: 2012/02514-9FAPESP: 2013/07763-0FAPESP: 2010/01404-0Web of Science-engPeerj IncPeerjRadical acetylationDiacetylFood additiveLung diseasesProteomicsIncreased chemical acetylation of peptides and proteins in rats after daily ingestion of diacetyl analyzed by Nano-LC-MS/MSinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleLondonv. 6info:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESPORIGINALWOS000430890200002.pdfapplication/pdf6858024${dspace.ui.url}/bitstream/11600/55628/1/WOS000430890200002.pdfac6e6cfa28281d2fd33d22b733afb64aMD51open accessTEXTWOS000430890200002.pdf.txtWOS000430890200002.pdf.txtExtracted texttext/plain53781${dspace.ui.url}/bitstream/11600/55628/8/WOS000430890200002.pdf.txt84d79ed5283f7718181e4adf13b22524MD58open accessTHUMBNAILWOS000430890200002.pdf.jpgWOS000430890200002.pdf.jpgIM Thumbnailimage/jpeg7263${dspace.ui.url}/bitstream/11600/55628/10/WOS000430890200002.pdf.jpg2daa525c99f064ed897156a4633fb858MD510open access11600/556282023-06-05 19:28:09.31open accessoai:repositorio.unifesp.br:11600/55628Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652023-06-05T22:28:09Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.en.fl_str_mv Increased chemical acetylation of peptides and proteins in rats after daily ingestion of diacetyl analyzed by Nano-LC-MS/MS
title Increased chemical acetylation of peptides and proteins in rats after daily ingestion of diacetyl analyzed by Nano-LC-MS/MS
spellingShingle Increased chemical acetylation of peptides and proteins in rats after daily ingestion of diacetyl analyzed by Nano-LC-MS/MS
Jedlicka, Leticia Dias Lima [UNIFESP]
Radical acetylation
Diacetyl
Food additive
Lung diseases
Proteomics
title_short Increased chemical acetylation of peptides and proteins in rats after daily ingestion of diacetyl analyzed by Nano-LC-MS/MS
title_full Increased chemical acetylation of peptides and proteins in rats after daily ingestion of diacetyl analyzed by Nano-LC-MS/MS
title_fullStr Increased chemical acetylation of peptides and proteins in rats after daily ingestion of diacetyl analyzed by Nano-LC-MS/MS
title_full_unstemmed Increased chemical acetylation of peptides and proteins in rats after daily ingestion of diacetyl analyzed by Nano-LC-MS/MS
title_sort Increased chemical acetylation of peptides and proteins in rats after daily ingestion of diacetyl analyzed by Nano-LC-MS/MS
author Jedlicka, Leticia Dias Lima [UNIFESP]
author_facet Jedlicka, Leticia Dias Lima [UNIFESP]
Guterres, Sheila Barreto [UNIFESP]
Balbino, Aleksandro Martins [UNIFESP]
Bruno Neto, Giuseppe [UNIFESP]
Landgraf, Richardt Gama [UNIFESP]
Fernandes, Liliam [UNIFESP]
Carrilho, Emanuel
Bechara, Etelvino José Henriques [UNIFESP]
Assunção, Nilson Antonio [UNIFESP]
author_role author
author2 Guterres, Sheila Barreto [UNIFESP]
Balbino, Aleksandro Martins [UNIFESP]
Bruno Neto, Giuseppe [UNIFESP]
Landgraf, Richardt Gama [UNIFESP]
Fernandes, Liliam [UNIFESP]
Carrilho, Emanuel
Bechara, Etelvino José Henriques [UNIFESP]
Assunção, Nilson Antonio [UNIFESP]
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Jedlicka, Leticia Dias Lima [UNIFESP]
Guterres, Sheila Barreto [UNIFESP]
Balbino, Aleksandro Martins [UNIFESP]
Bruno Neto, Giuseppe [UNIFESP]
Landgraf, Richardt Gama [UNIFESP]
Fernandes, Liliam [UNIFESP]
Carrilho, Emanuel
Bechara, Etelvino José Henriques [UNIFESP]
Assunção, Nilson Antonio [UNIFESP]
dc.subject.eng.fl_str_mv Radical acetylation
Diacetyl
Food additive
Lung diseases
Proteomics
topic Radical acetylation
Diacetyl
Food additive
Lung diseases
Proteomics
description Background. Acetylation alters several protein properties including molecular weight, stability, enzymatic activity, protein protein interactions, and other biological functions. Our previous findings demonstrating that diacetyl/peroxynitrite can acetylate L-lysine, L-histidine, and albumin in vitro led us to investigate whether diacetyl-treated rats suffer protein acetylation as well. Methods. Wistar rats were administered diacetyl daily for four weeks, after which they were sacrificed, and their lung proteins were extracted to be analysed by Nano-LC-MS/MS (Q-TOF). A C18 reversed-phase colurnn and gradient elution with formic acid/acetonitrile solutions from 2 to 50% over 150 min were used to separate the proteins. Protein detection was performed using a microTOE-Q II (QTOF) equipped with captive source and an electrospray-ionization source. The data frommass spectrometry were processed using a Compass 1.7 and analyzed using Protein Scape, software that uses Mascot algorithms to perform protein searches. Results. A set of 3,162 acetylated peptides derived from 351 acetylated proteins in the diacetyl-treated group was identified. Among them, 23 targeted proteins were significantly more acetylated in the diacetyl-treated group than in the PBS control. Protein acetylation of the group treated with 540 mg/kg/day of diacetyl was corroborated by Western blotting analysis. Conclusions. These data support our hypothesis that diacetyl exposure in animals may lead to the generation of acetyl radicals, compounds that attach to proteins, affecting their functions and triggering adverse health problems.
publishDate 2018
dc.date.issued.fl_str_mv 2018
dc.date.accessioned.fl_str_mv 2020-07-20T16:30:59Z
dc.date.available.fl_str_mv 2020-07-20T16:30:59Z
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dc.identifier.citation.fl_str_mv Peerj. London, v. 6, p. -, 2018.
dc.identifier.uri.fl_str_mv https://repositorio.unifesp.br/handle/11600/55628
http://dx.doi.org/10.7717/peerj.4688
dc.identifier.issn.none.fl_str_mv 2167-8359
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dc.identifier.doi.none.fl_str_mv 10.7717/peerj.4688
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identifier_str_mv Peerj. London, v. 6, p. -, 2018.
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WOS000430890200002.pdf
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