System-Wide Quantitative Proteomics of the Metabolic Syndrome in Mice: Genotypic and Dietary Effects
Advances in mass spectrometry have made the quantitative measurement of proteins across multiple samples a reality, allowing for the study of complex biological systems such as the metabolic syndrome. Although the deregulation of lipid metabolism and increased hepatic storage of triacylglycerides ar...
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Veröffentlicht in: | Journal of proteome research 2017-02, Vol.16 (2), p.831-841 |
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container_title | Journal of proteome research |
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creator | Terfve, Camille Sabidó, Eduard Wu, Yibo Gonçalves, Emanuel Choi, Meena Vaga, Stefania Vitek, Olga Saez-Rodriguez, Julio Aebersold, Ruedi |
description | Advances in mass spectrometry have made the quantitative measurement of proteins across multiple samples a reality, allowing for the study of complex biological systems such as the metabolic syndrome. Although the deregulation of lipid metabolism and increased hepatic storage of triacylglycerides are known to play a part in the onset of the metabolic syndrome, its molecular basis and dependency on dietary and genotypic factors are poorly characterized. Here, we used an experimental design with two different mouse strains and dietary and metabolic perturbations to generate a compendium of quantitative proteome data using three mass spectrometric techniques. The data reproduce known properties of the metabolic system and indicate differential molecular adaptation of the two mouse strains to perturbations, contributing to a better understanding of the metabolic syndrome. We show that high-quality, high-throughput proteomic data sets provide an unbiased broad overview of the behavior of complex systems after perturbation. |
doi_str_mv | 10.1021/acs.jproteome.6b00815 |
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Although the deregulation of lipid metabolism and increased hepatic storage of triacylglycerides are known to play a part in the onset of the metabolic syndrome, its molecular basis and dependency on dietary and genotypic factors are poorly characterized. Here, we used an experimental design with two different mouse strains and dietary and metabolic perturbations to generate a compendium of quantitative proteome data using three mass spectrometric techniques. The data reproduce known properties of the metabolic system and indicate differential molecular adaptation of the two mouse strains to perturbations, contributing to a better understanding of the metabolic syndrome. 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Proteome Res</addtitle><description>Advances in mass spectrometry have made the quantitative measurement of proteins across multiple samples a reality, allowing for the study of complex biological systems such as the metabolic syndrome. Although the deregulation of lipid metabolism and increased hepatic storage of triacylglycerides are known to play a part in the onset of the metabolic syndrome, its molecular basis and dependency on dietary and genotypic factors are poorly characterized. Here, we used an experimental design with two different mouse strains and dietary and metabolic perturbations to generate a compendium of quantitative proteome data using three mass spectrometric techniques. The data reproduce known properties of the metabolic system and indicate differential molecular adaptation of the two mouse strains to perturbations, contributing to a better understanding of the metabolic syndrome. We show that high-quality, high-throughput proteomic data sets provide an unbiased broad overview of the behavior of complex systems after perturbation.</description><subject>Animals</subject><subject>Cell Line</subject><subject>Diet, High-Fat - adverse effects</subject><subject>Disease Models, Animal</subject><subject>Gene Expression Regulation</subject><subject>Genotype</subject><subject>Hepatocytes - metabolism</subject><subject>Hepatocytes - pathology</subject><subject>Isotope Labeling</subject><subject>Liver - metabolism</subject><subject>Liver - pathology</subject><subject>Mass Spectrometry - methods</subject><subject>Metabolic Networks and Pathways - genetics</subject><subject>Metabolic Syndrome - etiology</subject><subject>Metabolic Syndrome - genetics</subject><subject>Metabolic Syndrome - metabolism</subject><subject>Metabolic Syndrome - pathology</subject><subject>Mice, 129 Strain</subject><subject>Mice, Inbred C57BL</subject><subject>Principal Component Analysis</subject><subject>Proteome - genetics</subject><subject>Proteome - isolation & purification</subject><subject>Proteome - metabolism</subject><subject>Triglycerides - isolation & purification</subject><subject>Triglycerides - metabolism</subject><issn>1535-3893</issn><issn>1535-3907</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkF1PwyAUhonRuDn9CRouvemEMlrwzsw5TbaomcbLhsIhsqztLNRk_150H7deQcLzvufwIHRJyZCSlN4o7YfLddsEaCoYZiUhgvIj1Kec8YRJkh_v70KyHjrzfkkI5Tlhp6iX5pJleUb6yCw2PkCVfDgD-LVTdXBBBfcN-GXb7bTHjcXhE_AcgiqbldN4salNG-diV-O503CLp1A3YbOOb6o2-N5FtN3gibWggz9HJ1atPFzszgF6f5i8jR-T2fP0aXw3SxSTIiR5SeN65SiVqU0VSJmPwAgpuIXSMCq0EmA0B2tzZoAyk9GUiBI4MSnPgLEBut72Ri9fHfhQVM5rWK1UDU3nCyp4mnFJslFE-RbVbeN9C7ZYt66KOxeUFL-Ciyi4OAgudoJj7mo3oisrMIfU3mgE6Bb4yzddW8cf_1P6AyCHjPo</recordid><startdate>20170203</startdate><enddate>20170203</enddate><creator>Terfve, Camille</creator><creator>Sabidó, Eduard</creator><creator>Wu, Yibo</creator><creator>Gonçalves, Emanuel</creator><creator>Choi, Meena</creator><creator>Vaga, Stefania</creator><creator>Vitek, Olga</creator><creator>Saez-Rodriguez, Julio</creator><creator>Aebersold, Ruedi</creator><general>American Chemical Society</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><orcidid>https://orcid.org/0000-0001-6506-7714</orcidid><orcidid>https://orcid.org/0000-0002-6025-5035</orcidid><orcidid>https://orcid.org/0000-0003-1728-1104</orcidid></search><sort><creationdate>20170203</creationdate><title>System-Wide Quantitative Proteomics of the Metabolic Syndrome in Mice: Genotypic and Dietary Effects</title><author>Terfve, Camille ; Sabidó, Eduard ; Wu, Yibo ; Gonçalves, Emanuel ; Choi, Meena ; Vaga, Stefania ; Vitek, Olga ; Saez-Rodriguez, Julio ; Aebersold, Ruedi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a398t-7b1703b4292f2ae9974ed8985febd318ca8edc5eff73de13d61208be50d256e33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Animals</topic><topic>Cell Line</topic><topic>Diet, High-Fat - adverse effects</topic><topic>Disease Models, Animal</topic><topic>Gene Expression Regulation</topic><topic>Genotype</topic><topic>Hepatocytes - metabolism</topic><topic>Hepatocytes - pathology</topic><topic>Isotope Labeling</topic><topic>Liver - metabolism</topic><topic>Liver - pathology</topic><topic>Mass Spectrometry - methods</topic><topic>Metabolic Networks and Pathways - genetics</topic><topic>Metabolic Syndrome - etiology</topic><topic>Metabolic Syndrome - genetics</topic><topic>Metabolic Syndrome - metabolism</topic><topic>Metabolic Syndrome - pathology</topic><topic>Mice, 129 Strain</topic><topic>Mice, Inbred C57BL</topic><topic>Principal Component Analysis</topic><topic>Proteome - genetics</topic><topic>Proteome - isolation & purification</topic><topic>Proteome - metabolism</topic><topic>Triglycerides - isolation & purification</topic><topic>Triglycerides - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Terfve, Camille</creatorcontrib><creatorcontrib>Sabidó, Eduard</creatorcontrib><creatorcontrib>Wu, Yibo</creatorcontrib><creatorcontrib>Gonçalves, Emanuel</creatorcontrib><creatorcontrib>Choi, Meena</creatorcontrib><creatorcontrib>Vaga, Stefania</creatorcontrib><creatorcontrib>Vitek, Olga</creatorcontrib><creatorcontrib>Saez-Rodriguez, Julio</creatorcontrib><creatorcontrib>Aebersold, Ruedi</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>Journal of proteome research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Terfve, Camille</au><au>Sabidó, Eduard</au><au>Wu, Yibo</au><au>Gonçalves, Emanuel</au><au>Choi, Meena</au><au>Vaga, Stefania</au><au>Vitek, Olga</au><au>Saez-Rodriguez, Julio</au><au>Aebersold, Ruedi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>System-Wide Quantitative Proteomics of the Metabolic Syndrome in Mice: Genotypic and Dietary Effects</atitle><jtitle>Journal of proteome research</jtitle><addtitle>J. Proteome Res</addtitle><date>2017-02-03</date><risdate>2017</risdate><volume>16</volume><issue>2</issue><spage>831</spage><epage>841</epage><pages>831-841</pages><issn>1535-3893</issn><eissn>1535-3907</eissn><abstract>Advances in mass spectrometry have made the quantitative measurement of proteins across multiple samples a reality, allowing for the study of complex biological systems such as the metabolic syndrome. Although the deregulation of lipid metabolism and increased hepatic storage of triacylglycerides are known to play a part in the onset of the metabolic syndrome, its molecular basis and dependency on dietary and genotypic factors are poorly characterized. Here, we used an experimental design with two different mouse strains and dietary and metabolic perturbations to generate a compendium of quantitative proteome data using three mass spectrometric techniques. 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subjects | Animals Cell Line Diet, High-Fat - adverse effects Disease Models, Animal Gene Expression Regulation Genotype Hepatocytes - metabolism Hepatocytes - pathology Isotope Labeling Liver - metabolism Liver - pathology Mass Spectrometry - methods Metabolic Networks and Pathways - genetics Metabolic Syndrome - etiology Metabolic Syndrome - genetics Metabolic Syndrome - metabolism Metabolic Syndrome - pathology Mice, 129 Strain Mice, Inbred C57BL Principal Component Analysis Proteome - genetics Proteome - isolation & purification Proteome - metabolism Triglycerides - isolation & purification Triglycerides - metabolism |
title | System-Wide Quantitative Proteomics of the Metabolic Syndrome in Mice: Genotypic and Dietary Effects |
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