Comparative Proteomic Analysis of Intra- and Interindividual Variation in Human Cerebrospinal Fluid
Cerebrospinal fluid (CSF) is a potential source of biomarkers for many disorders of the central nervous system, including Alzheimer disease (AD). Prior to comparing CSF samples between individuals to identify patterns of disease-associated proteins, it is important to examine variation within indivi...
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Veröffentlicht in: | Molecular & cellular proteomics 2005-12, Vol.4 (12), p.2000-2009 |
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container_title | Molecular & cellular proteomics |
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creator | Hu, Yan Malone, James P Fagan, Anne M Townsend, R Reid Holtzman, David M |
description | Cerebrospinal fluid (CSF) is a potential source of biomarkers for many disorders of the central nervous system, including
Alzheimer disease (AD). Prior to comparing CSF samples between individuals to identify patterns of disease-associated proteins,
it is important to examine variation within individuals over a short period of time so that one can better interpret potential
changes in CSF between individuals as well as changes within a given individual over a longer time span. In this study, we
analyzed 12 CSF samples, composed of pairs of samples from six individuals, obtained 2 weeks apart. Multiaffinity depletion,
two-dimensional DIGE, and tandem mass spectrometry were used. A number of proteins whose abundance varied between the two
time points was identified for each individual. Some of these proteins were commonly identified in multiple individuals. More
importantly, despite the intraindividual variations, hierarchical clustering and multidimensional scaling analysis of the
proteomic profiles revealed that two CSF samples from the same individual cluster the closest together and that the between-subject
variability is much larger than the within-subject variability. Among the six subjects, comparison between the four cognitively
normal and the two very mildly demented subjects also yielded some proteins that have been identified in previous AD biomarker
studies. These results validate our method of identifying differences in proteomic profiles of CSF samples and have important
implications for the design of CSF biomarker studies for AD and other central nervous system disorders. |
doi_str_mv | 10.1074/mcp.M500207-MCP200 |
format | Article |
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Alzheimer disease (AD). Prior to comparing CSF samples between individuals to identify patterns of disease-associated proteins,
it is important to examine variation within individuals over a short period of time so that one can better interpret potential
changes in CSF between individuals as well as changes within a given individual over a longer time span. In this study, we
analyzed 12 CSF samples, composed of pairs of samples from six individuals, obtained 2 weeks apart. Multiaffinity depletion,
two-dimensional DIGE, and tandem mass spectrometry were used. A number of proteins whose abundance varied between the two
time points was identified for each individual. Some of these proteins were commonly identified in multiple individuals. More
importantly, despite the intraindividual variations, hierarchical clustering and multidimensional scaling analysis of the
proteomic profiles revealed that two CSF samples from the same individual cluster the closest together and that the between-subject
variability is much larger than the within-subject variability. Among the six subjects, comparison between the four cognitively
normal and the two very mildly demented subjects also yielded some proteins that have been identified in previous AD biomarker
studies. These results validate our method of identifying differences in proteomic profiles of CSF samples and have important
implications for the design of CSF biomarker studies for AD and other central nervous system disorders.</description><identifier>ISSN: 1535-9476</identifier><identifier>EISSN: 1535-9484</identifier><identifier>DOI: 10.1074/mcp.M500207-MCP200</identifier><identifier>PMID: 16199891</identifier><language>eng</language><publisher>United States: American Society for Biochemistry and Molecular Biology</publisher><subject>Cerebrospinal Fluid Proteins - chemistry ; Cerebrospinal Fluid Proteins - isolation & purification ; Electrophoresis, Gel, Two-Dimensional ; Humans ; Mass Spectrometry ; Proteome - chemistry ; Proteome - genetics ; Proteomics - methods ; Reproducibility of Results</subject><ispartof>Molecular & cellular proteomics, 2005-12, Vol.4 (12), p.2000-2009</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c468t-cca6a6e4447ccdd9c4ff363d33381752d654255f487ee3a82cccae2e9a6fa1033</citedby><cites>FETCH-LOGICAL-c468t-cca6a6e4447ccdd9c4ff363d33381752d654255f487ee3a82cccae2e9a6fa1033</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16199891$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hu, Yan</creatorcontrib><creatorcontrib>Malone, James P</creatorcontrib><creatorcontrib>Fagan, Anne M</creatorcontrib><creatorcontrib>Townsend, R Reid</creatorcontrib><creatorcontrib>Holtzman, David M</creatorcontrib><title>Comparative Proteomic Analysis of Intra- and Interindividual Variation in Human Cerebrospinal Fluid</title><title>Molecular & cellular proteomics</title><addtitle>Mol Cell Proteomics</addtitle><description>Cerebrospinal fluid (CSF) is a potential source of biomarkers for many disorders of the central nervous system, including
Alzheimer disease (AD). Prior to comparing CSF samples between individuals to identify patterns of disease-associated proteins,
it is important to examine variation within individuals over a short period of time so that one can better interpret potential
changes in CSF between individuals as well as changes within a given individual over a longer time span. In this study, we
analyzed 12 CSF samples, composed of pairs of samples from six individuals, obtained 2 weeks apart. Multiaffinity depletion,
two-dimensional DIGE, and tandem mass spectrometry were used. A number of proteins whose abundance varied between the two
time points was identified for each individual. Some of these proteins were commonly identified in multiple individuals. More
importantly, despite the intraindividual variations, hierarchical clustering and multidimensional scaling analysis of the
proteomic profiles revealed that two CSF samples from the same individual cluster the closest together and that the between-subject
variability is much larger than the within-subject variability. Among the six subjects, comparison between the four cognitively
normal and the two very mildly demented subjects also yielded some proteins that have been identified in previous AD biomarker
studies. These results validate our method of identifying differences in proteomic profiles of CSF samples and have important
implications for the design of CSF biomarker studies for AD and other central nervous system disorders.</description><subject>Cerebrospinal Fluid Proteins - chemistry</subject><subject>Cerebrospinal Fluid Proteins - isolation & purification</subject><subject>Electrophoresis, Gel, Two-Dimensional</subject><subject>Humans</subject><subject>Mass Spectrometry</subject><subject>Proteome - chemistry</subject><subject>Proteome - genetics</subject><subject>Proteomics - methods</subject><subject>Reproducibility of Results</subject><issn>1535-9476</issn><issn>1535-9484</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkTlv3DAQhQkjhq_4D6QImMadbN6iSkOID8BGtkjSElxy5GUgiQopOdh_by52YZepZorvvTkeQl8ouaakFjeDm66fJSGM1NVzu2KEHKEzKrmsGqHFp_e-VqfoPOc_O5LW8gSdUkWbRjf0DLk2DpNNdg6vgFcpzhCH4PDtaPttDhnHDj-Oc7IVtqPftZDC6MNr8Ivt8W-bQpHGEYcRPyyDHXELCdYp5ikUC3zXL8F_Rsed7TNcHuoF-nX3_Wf7UD39uH9sb58qJ5SeK-essgqEELVz3jdOdB1X3HPOdVmbeSUFk7ITugbgVjNXFMCgsaqzlHB-ga72vlOKfxfIsxlCdtD3doS4ZKO0rlVD5H9BRqTmDSMFZHvQlYtygs5MKQw2bQ0lZpeBKRmYQwZmn0ERfT24L-sB_Ifk8PQCfNsDm_Cy-RcSmHWIbgODEYayMr2YvAHDpY-S</recordid><startdate>20051201</startdate><enddate>20051201</enddate><creator>Hu, Yan</creator><creator>Malone, James P</creator><creator>Fagan, Anne M</creator><creator>Townsend, R Reid</creator><creator>Holtzman, David M</creator><general>American Society for Biochemistry and Molecular Biology</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>7TK</scope><scope>7X8</scope></search><sort><creationdate>20051201</creationdate><title>Comparative Proteomic Analysis of Intra- and Interindividual Variation in Human Cerebrospinal Fluid</title><author>Hu, Yan ; Malone, James P ; Fagan, Anne M ; Townsend, R Reid ; Holtzman, David M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c468t-cca6a6e4447ccdd9c4ff363d33381752d654255f487ee3a82cccae2e9a6fa1033</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Cerebrospinal Fluid Proteins - chemistry</topic><topic>Cerebrospinal Fluid Proteins - isolation & purification</topic><topic>Electrophoresis, Gel, Two-Dimensional</topic><topic>Humans</topic><topic>Mass Spectrometry</topic><topic>Proteome - chemistry</topic><topic>Proteome - genetics</topic><topic>Proteomics - methods</topic><topic>Reproducibility of Results</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hu, Yan</creatorcontrib><creatorcontrib>Malone, James P</creatorcontrib><creatorcontrib>Fagan, Anne M</creatorcontrib><creatorcontrib>Townsend, R Reid</creatorcontrib><creatorcontrib>Holtzman, David M</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular & cellular proteomics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hu, Yan</au><au>Malone, James P</au><au>Fagan, Anne M</au><au>Townsend, R Reid</au><au>Holtzman, David M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparative Proteomic Analysis of Intra- and Interindividual Variation in Human Cerebrospinal Fluid</atitle><jtitle>Molecular & cellular proteomics</jtitle><addtitle>Mol Cell Proteomics</addtitle><date>2005-12-01</date><risdate>2005</risdate><volume>4</volume><issue>12</issue><spage>2000</spage><epage>2009</epage><pages>2000-2009</pages><issn>1535-9476</issn><eissn>1535-9484</eissn><abstract>Cerebrospinal fluid (CSF) is a potential source of biomarkers for many disorders of the central nervous system, including
Alzheimer disease (AD). Prior to comparing CSF samples between individuals to identify patterns of disease-associated proteins,
it is important to examine variation within individuals over a short period of time so that one can better interpret potential
changes in CSF between individuals as well as changes within a given individual over a longer time span. In this study, we
analyzed 12 CSF samples, composed of pairs of samples from six individuals, obtained 2 weeks apart. Multiaffinity depletion,
two-dimensional DIGE, and tandem mass spectrometry were used. A number of proteins whose abundance varied between the two
time points was identified for each individual. Some of these proteins were commonly identified in multiple individuals. More
importantly, despite the intraindividual variations, hierarchical clustering and multidimensional scaling analysis of the
proteomic profiles revealed that two CSF samples from the same individual cluster the closest together and that the between-subject
variability is much larger than the within-subject variability. Among the six subjects, comparison between the four cognitively
normal and the two very mildly demented subjects also yielded some proteins that have been identified in previous AD biomarker
studies. These results validate our method of identifying differences in proteomic profiles of CSF samples and have important
implications for the design of CSF biomarker studies for AD and other central nervous system disorders.</abstract><cop>United States</cop><pub>American Society for Biochemistry and Molecular Biology</pub><pmid>16199891</pmid><doi>10.1074/mcp.M500207-MCP200</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection; Free Full-Text Journals in Chemistry |
subjects | Cerebrospinal Fluid Proteins - chemistry Cerebrospinal Fluid Proteins - isolation & purification Electrophoresis, Gel, Two-Dimensional Humans Mass Spectrometry Proteome - chemistry Proteome - genetics Proteomics - methods Reproducibility of Results |
title | Comparative Proteomic Analysis of Intra- and Interindividual Variation in Human Cerebrospinal Fluid |
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