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Label-free quantitative proteomic analysis of human plasma-derived microvesicles to find protein signatures of abdominal aortic aneurysms
Purpose To find potential biomarkers of abdominal aortic aneurysms (AAA), we performed a differential proteomic study based on human plasma‐derived microvesicles. Experimental design Exosomes and microparticles isolated from plasma of AAA patients and control subjects (n = 10 each group) were analyz...
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Published in: | Proteomics. Clinical applications 2014-08, Vol.8 (7-8), p.620-625 |
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container_title | Proteomics. Clinical applications |
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creator | Martinez-Pinna, Roxana de Peredo, Anne Gonzalez Monsarrat, Bernard Burlet-Schiltz, Odile Martin-Ventura, Jose Luis |
description | Purpose
To find potential biomarkers of abdominal aortic aneurysms (AAA), we performed a differential proteomic study based on human plasma‐derived microvesicles.
Experimental design
Exosomes and microparticles isolated from plasma of AAA patients and control subjects (n = 10 each group) were analyzed by a label‐free quantitative MS‐based strategy. Homemade and publicly available software packages have been used for MS data analysis.
Results
The application of two kinds of bioinformatic tools allowed us to find differential protein profiles from AAA patients. Some of these proteins found by the two analysis methods belong to main pathological mechanisms of AAA such as oxidative stress, immune‐inflammation, and thrombosis.
Conclusions and clinical relevance
Data analysis from label‐free MS‐based experiments requires the use of sophisticated bioinformatic approaches to perform quantitative studies from complex protein mixtures. The application of two of these bioinformatic tools provided us a preliminary list of differential proteins found in plasma‐derived microvesicles not previously associated to AAA, which could help us to understand the pathological mechanisms related to this disease. |
doi_str_mv | 10.1002/prca.201400010 |
format | article |
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To find potential biomarkers of abdominal aortic aneurysms (AAA), we performed a differential proteomic study based on human plasma‐derived microvesicles.
Experimental design
Exosomes and microparticles isolated from plasma of AAA patients and control subjects (n = 10 each group) were analyzed by a label‐free quantitative MS‐based strategy. Homemade and publicly available software packages have been used for MS data analysis.
Results
The application of two kinds of bioinformatic tools allowed us to find differential protein profiles from AAA patients. Some of these proteins found by the two analysis methods belong to main pathological mechanisms of AAA such as oxidative stress, immune‐inflammation, and thrombosis.
Conclusions and clinical relevance
Data analysis from label‐free MS‐based experiments requires the use of sophisticated bioinformatic approaches to perform quantitative studies from complex protein mixtures. The application of two of these bioinformatic tools provided us a preliminary list of differential proteins found in plasma‐derived microvesicles not previously associated to AAA, which could help us to understand the pathological mechanisms related to this disease.</description><identifier>ISSN: 1862-8346</identifier><identifier>EISSN: 1862-8354</identifier><identifier>DOI: 10.1002/prca.201400010</identifier><identifier>PMID: 24888668</identifier><language>eng</language><publisher>Germany: Blackwell Publishing Ltd</publisher><subject>Abdominal aortic aneurysm ; Aneurysms ; Aortic Aneurysm, Abdominal - blood ; Aortic Aneurysm, Abdominal - metabolism ; Aortic Aneurysm, Abdominal - pathology ; Data analysis ; Exosomes - metabolism ; Humans ; Microvesicles ; Plasma ; Proteins ; Proteomics - methods</subject><ispartof>Proteomics. Clinical applications, 2014-08, Vol.8 (7-8), p.620-625</ispartof><rights>2014 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.</rights><rights>2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5050-340ce5ef9c7885710ba3a5c29c13301e95df2522ef78266e3e01f97a9b7f947c3</citedby><cites>FETCH-LOGICAL-c5050-340ce5ef9c7885710ba3a5c29c13301e95df2522ef78266e3e01f97a9b7f947c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24888668$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Martinez-Pinna, Roxana</creatorcontrib><creatorcontrib>de Peredo, Anne Gonzalez</creatorcontrib><creatorcontrib>Monsarrat, Bernard</creatorcontrib><creatorcontrib>Burlet-Schiltz, Odile</creatorcontrib><creatorcontrib>Martin-Ventura, Jose Luis</creatorcontrib><title>Label-free quantitative proteomic analysis of human plasma-derived microvesicles to find protein signatures of abdominal aortic aneurysms</title><title>Proteomics. Clinical applications</title><addtitle>Prot. Clin. Appl</addtitle><description>Purpose
To find potential biomarkers of abdominal aortic aneurysms (AAA), we performed a differential proteomic study based on human plasma‐derived microvesicles.
Experimental design
Exosomes and microparticles isolated from plasma of AAA patients and control subjects (n = 10 each group) were analyzed by a label‐free quantitative MS‐based strategy. Homemade and publicly available software packages have been used for MS data analysis.
Results
The application of two kinds of bioinformatic tools allowed us to find differential protein profiles from AAA patients. Some of these proteins found by the two analysis methods belong to main pathological mechanisms of AAA such as oxidative stress, immune‐inflammation, and thrombosis.
Conclusions and clinical relevance
Data analysis from label‐free MS‐based experiments requires the use of sophisticated bioinformatic approaches to perform quantitative studies from complex protein mixtures. The application of two of these bioinformatic tools provided us a preliminary list of differential proteins found in plasma‐derived microvesicles not previously associated to AAA, which could help us to understand the pathological mechanisms related to this disease.</description><subject>Abdominal aortic aneurysm</subject><subject>Aneurysms</subject><subject>Aortic Aneurysm, Abdominal - blood</subject><subject>Aortic Aneurysm, Abdominal - metabolism</subject><subject>Aortic Aneurysm, Abdominal - pathology</subject><subject>Data analysis</subject><subject>Exosomes - metabolism</subject><subject>Humans</subject><subject>Microvesicles</subject><subject>Plasma</subject><subject>Proteins</subject><subject>Proteomics - methods</subject><issn>1862-8346</issn><issn>1862-8354</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqNkb1uFDEYRUcIRH6gpUSWaGhm-WyPx3YZrUiCtIKAgigtj-czOMzPxp4J7CPw1ngzYQsaqOzi3KNr36J4QWFFAdibbXR2xYBWAEDhUXFMVc1KxUX1-HCv6qPiJKUbAFExCU-LI1YppepaHRe_NrbBrvQRkdzOdpjCZKdwh2QbxwnHPjhiB9vtUkhk9OTb3NuBbDubelu2GDPZkgzF8Q5TcB0mMo3Eh6FdBGEgKXwd7DRHvBfYps3SbCR2jNO9Hee4S316Vjzxtkv4_OE8LT6fv71eX5abDxfv1meb0gkQUPIKHAr02kmlhKTQWG6FY9pRzoGiFq1ngjH0UrG6Ro5AvZZWN9LrSjp-WrxevLng7YxpMn1IDrsuNxnnZKiogVIpBP0PVHAJutaQ0Vd_oTfjHPM7F4ppraXK1Gqh8oelFNGbbQy9jTtDwez3NPs9zWHPHHj5oJ2bHtsD_mfADFQL8CN0uPuHzlx9Wp_lOntvucRCmvDnIWbjd1NLLoX58v7C6OsrxuT6oznnvwFhxLxW</recordid><startdate>201408</startdate><enddate>201408</enddate><creator>Martinez-Pinna, Roxana</creator><creator>de Peredo, Anne Gonzalez</creator><creator>Monsarrat, Bernard</creator><creator>Burlet-Schiltz, Odile</creator><creator>Martin-Ventura, Jose Luis</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><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>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>7QO</scope></search><sort><creationdate>201408</creationdate><title>Label-free quantitative proteomic analysis of human plasma-derived microvesicles to find protein signatures of abdominal aortic aneurysms</title><author>Martinez-Pinna, Roxana ; de Peredo, Anne Gonzalez ; Monsarrat, Bernard ; Burlet-Schiltz, Odile ; Martin-Ventura, Jose Luis</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5050-340ce5ef9c7885710ba3a5c29c13301e95df2522ef78266e3e01f97a9b7f947c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Abdominal aortic aneurysm</topic><topic>Aneurysms</topic><topic>Aortic Aneurysm, Abdominal - blood</topic><topic>Aortic Aneurysm, Abdominal - metabolism</topic><topic>Aortic Aneurysm, Abdominal - pathology</topic><topic>Data analysis</topic><topic>Exosomes - metabolism</topic><topic>Humans</topic><topic>Microvesicles</topic><topic>Plasma</topic><topic>Proteins</topic><topic>Proteomics - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Martinez-Pinna, Roxana</creatorcontrib><creatorcontrib>de Peredo, Anne Gonzalez</creatorcontrib><creatorcontrib>Monsarrat, Bernard</creatorcontrib><creatorcontrib>Burlet-Schiltz, Odile</creatorcontrib><creatorcontrib>Martin-Ventura, Jose Luis</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><jtitle>Proteomics. Clinical applications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Martinez-Pinna, Roxana</au><au>de Peredo, Anne Gonzalez</au><au>Monsarrat, Bernard</au><au>Burlet-Schiltz, Odile</au><au>Martin-Ventura, Jose Luis</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Label-free quantitative proteomic analysis of human plasma-derived microvesicles to find protein signatures of abdominal aortic aneurysms</atitle><jtitle>Proteomics. Clinical applications</jtitle><addtitle>Prot. Clin. Appl</addtitle><date>2014-08</date><risdate>2014</risdate><volume>8</volume><issue>7-8</issue><spage>620</spage><epage>625</epage><pages>620-625</pages><issn>1862-8346</issn><eissn>1862-8354</eissn><abstract>Purpose
To find potential biomarkers of abdominal aortic aneurysms (AAA), we performed a differential proteomic study based on human plasma‐derived microvesicles.
Experimental design
Exosomes and microparticles isolated from plasma of AAA patients and control subjects (n = 10 each group) were analyzed by a label‐free quantitative MS‐based strategy. Homemade and publicly available software packages have been used for MS data analysis.
Results
The application of two kinds of bioinformatic tools allowed us to find differential protein profiles from AAA patients. Some of these proteins found by the two analysis methods belong to main pathological mechanisms of AAA such as oxidative stress, immune‐inflammation, and thrombosis.
Conclusions and clinical relevance
Data analysis from label‐free MS‐based experiments requires the use of sophisticated bioinformatic approaches to perform quantitative studies from complex protein mixtures. The application of two of these bioinformatic tools provided us a preliminary list of differential proteins found in plasma‐derived microvesicles not previously associated to AAA, which could help us to understand the pathological mechanisms related to this disease.</abstract><cop>Germany</cop><pub>Blackwell Publishing Ltd</pub><pmid>24888668</pmid><doi>10.1002/prca.201400010</doi><tpages>6</tpages></addata></record> |
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subjects | Abdominal aortic aneurysm Aneurysms Aortic Aneurysm, Abdominal - blood Aortic Aneurysm, Abdominal - metabolism Aortic Aneurysm, Abdominal - pathology Data analysis Exosomes - metabolism Humans Microvesicles Plasma Proteins Proteomics - methods |
title | Label-free quantitative proteomic analysis of human plasma-derived microvesicles to find protein signatures of abdominal aortic aneurysms |
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