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Metalloproteomic and differential expression in plasma in a rat model of type 1 diabetes
•Metalloproteomic and differential expression in plasma.•Protein separation by a two-dimensional gel electrophoresis.•Identification of cooper, selenium and zinc present in the protein spots by FAAS or GFASS.•It was possible to characterize 35 protein spots by ESI–MS/MS. Type 1 diabetes is character...
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Published in: | International journal of biological macromolecules 2017-11, Vol.104 (Pt A), p.414-422 |
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container_issue | Pt A |
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container_title | International journal of biological macromolecules |
container_volume | 104 |
creator | Pereira Braga, Camila Cavalcante Souza Vieira, José Lima Leite, Aline de Henrique Fernandes, Ana Angélica Rabelo Buzalaf, Marília Afonso Magalhães Padilha, Pedro de |
description | •Metalloproteomic and differential expression in plasma.•Protein separation by a two-dimensional gel electrophoresis.•Identification of cooper, selenium and zinc present in the protein spots by FAAS or GFASS.•It was possible to characterize 35 protein spots by ESI–MS/MS.
Type 1 diabetes is characterized by hyperglycemia, which in the chronic stage is associated with abnormalities in lipids, protein and, carbohydrate metabolism, as well as oxidative stress. New strategies for prevention and treatment are needed, as type 1 diabetes affects life quality and survival, and involves high-cost treatment. Proteomic and metalloproteomic studies can elucidate the functional and physiological aspects of biomolecules. In the present study, differential proteomics was used to identify potential biomarkers of diabetes in rat plasma associated with copper, selenium, zinc, and magnesium fractionation in control and diabetic rats, as well as diabetic rats treated with insulin. 2D-PAGE was used in the plasma protein fractionation; graphite furnace atomic absorption spectrometry (GFAAS) and flame atomic absorption spectrometry (FAAS) were used for quantitative determination of copper, magnesium, selenium, and zinc in the spots that showed different expression; and protein spots were characterized by electrospray ionization-tandem mass spectrometry (ESI–MS/MS) after tryptic digestion. ESI–MS/MS analysis characterized 35 different proteins, indicating alpha-1-macroglobulin and haptoglobulin as potential candidates as biomarkers for diabetes treated with insulin; also, 2′-deoxynucleoside 5′-phosphate N-hydrolase 1, transmembrane protein 11, serum amyloid P component, vitamin D-binding protein, and biliverdin reductase were identified as potential candidates as biomarkers for uncontrolled diabetes. |
doi_str_mv | 10.1016/j.ijbiomac.2017.06.032 |
format | article |
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Type 1 diabetes is characterized by hyperglycemia, which in the chronic stage is associated with abnormalities in lipids, protein and, carbohydrate metabolism, as well as oxidative stress. New strategies for prevention and treatment are needed, as type 1 diabetes affects life quality and survival, and involves high-cost treatment. Proteomic and metalloproteomic studies can elucidate the functional and physiological aspects of biomolecules. In the present study, differential proteomics was used to identify potential biomarkers of diabetes in rat plasma associated with copper, selenium, zinc, and magnesium fractionation in control and diabetic rats, as well as diabetic rats treated with insulin. 2D-PAGE was used in the plasma protein fractionation; graphite furnace atomic absorption spectrometry (GFAAS) and flame atomic absorption spectrometry (FAAS) were used for quantitative determination of copper, magnesium, selenium, and zinc in the spots that showed different expression; and protein spots were characterized by electrospray ionization-tandem mass spectrometry (ESI–MS/MS) after tryptic digestion. ESI–MS/MS analysis characterized 35 different proteins, indicating alpha-1-macroglobulin and haptoglobulin as potential candidates as biomarkers for diabetes treated with insulin; also, 2′-deoxynucleoside 5′-phosphate N-hydrolase 1, transmembrane protein 11, serum amyloid P component, vitamin D-binding protein, and biliverdin reductase were identified as potential candidates as biomarkers for uncontrolled diabetes.</description><identifier>ISSN: 0141-8130</identifier><identifier>EISSN: 1879-0003</identifier><identifier>DOI: 10.1016/j.ijbiomac.2017.06.032</identifier><identifier>PMID: 28601647</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Diabetes Mellitus, Type 1 - blood ; Diabetes Mellitus, Type 1 - metabolism ; Differential proteomic ; Disease Models, Animal ; Gene Expression Profiling ; Male ; Metalloproteins - blood ; Metalloproteins - metabolism ; Metalloproteomic ; Proteomics ; Rats ; Rats, Wistar ; Type 1 diabetes</subject><ispartof>International journal of biological macromolecules, 2017-11, Vol.104 (Pt A), p.414-422</ispartof><rights>2017 Elsevier B.V.</rights><rights>Copyright © 2017 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c416t-34990cec2045998757baa91ffd9ce839ea23cf6b33e0704b0c420c13aa9962f43</citedby><cites>FETCH-LOGICAL-c416t-34990cec2045998757baa91ffd9ce839ea23cf6b33e0704b0c420c13aa9962f43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27906,27907</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28601647$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pereira Braga, Camila</creatorcontrib><creatorcontrib>Cavalcante Souza Vieira, José</creatorcontrib><creatorcontrib>Lima Leite, Aline de</creatorcontrib><creatorcontrib>Henrique Fernandes, Ana Angélica</creatorcontrib><creatorcontrib>Rabelo Buzalaf, Marília Afonso</creatorcontrib><creatorcontrib>Magalhães Padilha, Pedro de</creatorcontrib><title>Metalloproteomic and differential expression in plasma in a rat model of type 1 diabetes</title><title>International journal of biological macromolecules</title><addtitle>Int J Biol Macromol</addtitle><description>•Metalloproteomic and differential expression in plasma.•Protein separation by a two-dimensional gel electrophoresis.•Identification of cooper, selenium and zinc present in the protein spots by FAAS or GFASS.•It was possible to characterize 35 protein spots by ESI–MS/MS.
Type 1 diabetes is characterized by hyperglycemia, which in the chronic stage is associated with abnormalities in lipids, protein and, carbohydrate metabolism, as well as oxidative stress. New strategies for prevention and treatment are needed, as type 1 diabetes affects life quality and survival, and involves high-cost treatment. Proteomic and metalloproteomic studies can elucidate the functional and physiological aspects of biomolecules. In the present study, differential proteomics was used to identify potential biomarkers of diabetes in rat plasma associated with copper, selenium, zinc, and magnesium fractionation in control and diabetic rats, as well as diabetic rats treated with insulin. 2D-PAGE was used in the plasma protein fractionation; graphite furnace atomic absorption spectrometry (GFAAS) and flame atomic absorption spectrometry (FAAS) were used for quantitative determination of copper, magnesium, selenium, and zinc in the spots that showed different expression; and protein spots were characterized by electrospray ionization-tandem mass spectrometry (ESI–MS/MS) after tryptic digestion. ESI–MS/MS analysis characterized 35 different proteins, indicating alpha-1-macroglobulin and haptoglobulin as potential candidates as biomarkers for diabetes treated with insulin; also, 2′-deoxynucleoside 5′-phosphate N-hydrolase 1, transmembrane protein 11, serum amyloid P component, vitamin D-binding protein, and biliverdin reductase were identified as potential candidates as biomarkers for uncontrolled diabetes.</description><subject>Animals</subject><subject>Diabetes Mellitus, Type 1 - blood</subject><subject>Diabetes Mellitus, Type 1 - metabolism</subject><subject>Differential proteomic</subject><subject>Disease Models, Animal</subject><subject>Gene Expression Profiling</subject><subject>Male</subject><subject>Metalloproteins - blood</subject><subject>Metalloproteins - metabolism</subject><subject>Metalloproteomic</subject><subject>Proteomics</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Type 1 diabetes</subject><issn>0141-8130</issn><issn>1879-0003</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNqFkE1LxDAQhoMoun78BcnRS-uk6abNTRG_YMWLgreQphPI0jY1yYr-e7OsevU0w_C8M8xDyDmDkgETl-vSrTvnR23KClhTgiiBV3tkwdpGFgDA98kCWM2KlnE4IscxrvNULFl7SI6qVuQldbMgb0-Y9DD4OfiEfnSG6qmnvbMWA07J6YHi5xwwRucn6iY6DzqOettpGnSio-9xoN7S9DUjZTmqO0wYT8mB1UPEs596Ql7vbl9uHorV8_3jzfWqMDUTqeC1lGDQVFAvpWybZdNpLZm1vTTYcom64saKjnOEBuoOTF2BYTxDUlS25ifkYrc3f_C-wZjU6KLBYdAT-k1UTEI2smSiyqjYoSb4GANaNQc36vClGKitVbVWv1bV1qoCobLVHDz_ubHpRuz_Yr8aM3C1AzB_-uEwqGgcTgZ7F9Ak1Xv3341vVJSL7w</recordid><startdate>201711</startdate><enddate>201711</enddate><creator>Pereira Braga, Camila</creator><creator>Cavalcante Souza Vieira, José</creator><creator>Lima Leite, Aline de</creator><creator>Henrique Fernandes, Ana Angélica</creator><creator>Rabelo Buzalaf, Marília Afonso</creator><creator>Magalhães Padilha, Pedro de</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201711</creationdate><title>Metalloproteomic and differential expression in plasma in a rat model of type 1 diabetes</title><author>Pereira Braga, Camila ; Cavalcante Souza Vieira, José ; Lima Leite, Aline de ; Henrique Fernandes, Ana Angélica ; Rabelo Buzalaf, Marília Afonso ; Magalhães Padilha, Pedro de</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c416t-34990cec2045998757baa91ffd9ce839ea23cf6b33e0704b0c420c13aa9962f43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Animals</topic><topic>Diabetes Mellitus, Type 1 - blood</topic><topic>Diabetes Mellitus, Type 1 - metabolism</topic><topic>Differential proteomic</topic><topic>Disease Models, Animal</topic><topic>Gene Expression Profiling</topic><topic>Male</topic><topic>Metalloproteins - blood</topic><topic>Metalloproteins - metabolism</topic><topic>Metalloproteomic</topic><topic>Proteomics</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Type 1 diabetes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pereira Braga, Camila</creatorcontrib><creatorcontrib>Cavalcante Souza Vieira, José</creatorcontrib><creatorcontrib>Lima Leite, Aline de</creatorcontrib><creatorcontrib>Henrique Fernandes, Ana Angélica</creatorcontrib><creatorcontrib>Rabelo Buzalaf, Marília Afonso</creatorcontrib><creatorcontrib>Magalhães Padilha, Pedro de</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of biological macromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pereira Braga, Camila</au><au>Cavalcante Souza Vieira, José</au><au>Lima Leite, Aline de</au><au>Henrique Fernandes, Ana Angélica</au><au>Rabelo Buzalaf, Marília Afonso</au><au>Magalhães Padilha, Pedro de</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metalloproteomic and differential expression in plasma in a rat model of type 1 diabetes</atitle><jtitle>International journal of biological macromolecules</jtitle><addtitle>Int J Biol Macromol</addtitle><date>2017-11</date><risdate>2017</risdate><volume>104</volume><issue>Pt A</issue><spage>414</spage><epage>422</epage><pages>414-422</pages><issn>0141-8130</issn><eissn>1879-0003</eissn><abstract>•Metalloproteomic and differential expression in plasma.•Protein separation by a two-dimensional gel electrophoresis.•Identification of cooper, selenium and zinc present in the protein spots by FAAS or GFASS.•It was possible to characterize 35 protein spots by ESI–MS/MS.
Type 1 diabetes is characterized by hyperglycemia, which in the chronic stage is associated with abnormalities in lipids, protein and, carbohydrate metabolism, as well as oxidative stress. New strategies for prevention and treatment are needed, as type 1 diabetes affects life quality and survival, and involves high-cost treatment. Proteomic and metalloproteomic studies can elucidate the functional and physiological aspects of biomolecules. In the present study, differential proteomics was used to identify potential biomarkers of diabetes in rat plasma associated with copper, selenium, zinc, and magnesium fractionation in control and diabetic rats, as well as diabetic rats treated with insulin. 2D-PAGE was used in the plasma protein fractionation; graphite furnace atomic absorption spectrometry (GFAAS) and flame atomic absorption spectrometry (FAAS) were used for quantitative determination of copper, magnesium, selenium, and zinc in the spots that showed different expression; and protein spots were characterized by electrospray ionization-tandem mass spectrometry (ESI–MS/MS) after tryptic digestion. ESI–MS/MS analysis characterized 35 different proteins, indicating alpha-1-macroglobulin and haptoglobulin as potential candidates as biomarkers for diabetes treated with insulin; also, 2′-deoxynucleoside 5′-phosphate N-hydrolase 1, transmembrane protein 11, serum amyloid P component, vitamin D-binding protein, and biliverdin reductase were identified as potential candidates as biomarkers for uncontrolled diabetes.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>28601647</pmid><doi>10.1016/j.ijbiomac.2017.06.032</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Diabetes Mellitus, Type 1 - blood Diabetes Mellitus, Type 1 - metabolism Differential proteomic Disease Models, Animal Gene Expression Profiling Male Metalloproteins - blood Metalloproteins - metabolism Metalloproteomic Proteomics Rats Rats, Wistar Type 1 diabetes |
title | Metalloproteomic and differential expression in plasma in a rat model of type 1 diabetes |
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