Label-free quantification using MALDI mass spectrometry: considerations and perspectives
Profound knowledge of protein abundances in healthy tissues and their changes in disease is crucial for understanding biological processes in basic science and for the development of novel diagnostics and therapeutics. Mass spectrometrybased label-free protein quantification is used increasingly oft...
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Veröffentlicht in: | Analytical and bioanalytical chemistry 2012-09, Vol.404 (4), p.1039-1056 |
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description | Profound knowledge of protein abundances in healthy tissues and their changes in disease is crucial for understanding biological processes in basic science and for the development of novel diagnostics and therapeutics. Mass spectrometrybased label-free protein quantification is used increasingly often to gain insights into physiological changes observed in perturbed systems. Although the soft ionization techniques electrospray ionization and matrix-assisted laser desorption/ionization have both been used for protein quantification, this article focuses on instrumental setups with a MALDI ion source. Beside reviewing current bioinformatic data-processing tools for label-free quantification and elaborating on the technical benefits of combining UHPLC and MALDI–MS, we outline the potential of state-of-the-art instruments by reporting unpublished results obtained from twenty-four complex biological samples. This review points out that the capabilities of LC–MALDI MS systems have not yet been fully utilized because of a lack of suitable software tools.
Online Abstract Figure
Graphical representation of the LC–MALDI–MS procedure for label-free protein quantification. Tryptic peptides are separated by reversed-phase ultra-high performance liquid chromatography and eluting fractions are mixed with matrix before robotic deposition on a MALDI target plate. Subsequent to analysis of each spot by MS
1
and MS
2
, bioinformatic tools are used for the label-free protein quantification |
doi_str_mv | 10.1007/s00216-012-5832-y |
format | Article |
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Online Abstract Figure
Graphical representation of the LC–MALDI–MS procedure for label-free protein quantification. Tryptic peptides are separated by reversed-phase ultra-high performance liquid chromatography and eluting fractions are mixed with matrix before robotic deposition on a MALDI target plate. Subsequent to analysis of each spot by MS
1
and MS
2
, bioinformatic tools are used for the label-free protein quantification</description><identifier>ISSN: 1618-2642</identifier><identifier>EISSN: 1618-2650</identifier><identifier>DOI: 10.1007/s00216-012-5832-y</identifier><identifier>PMID: 22358999</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer-Verlag</publisher><subject>Analytical Chemistry ; Animals ; Biochemistry ; Bioinformatics ; Biological ; Characterization and Evaluation of Materials ; Chemistry ; Chemistry and Materials Science ; Chromatography, High Pressure Liquid ; Computer programs ; Food Science ; Graphical representations ; Humans ; Ionization ; Laboratory Medicine ; Liquid chromatography ; Monitoring/Environmental Analysis ; Peptides ; Proteins ; Proteins - chemistry ; Proteomics - methods ; Proteomics - trends ; Review ; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - methods ; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - trends</subject><ispartof>Analytical and bioanalytical chemistry, 2012-09, Vol.404 (4), p.1039-1056</ispartof><rights>Springer-Verlag 2012</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c410t-2f3793eaeeec1e15f966ebb5ceb82029077d4b65361ea387ccfc0c2b36226fd23</citedby><cites>FETCH-LOGICAL-c410t-2f3793eaeeec1e15f966ebb5ceb82029077d4b65361ea387ccfc0c2b36226fd23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00216-012-5832-y$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00216-012-5832-y$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22358999$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Benk, Amelie S.</creatorcontrib><creatorcontrib>Roesli, Christoph</creatorcontrib><title>Label-free quantification using MALDI mass spectrometry: considerations and perspectives</title><title>Analytical and bioanalytical chemistry</title><addtitle>Anal Bioanal Chem</addtitle><addtitle>Anal Bioanal Chem</addtitle><description>Profound knowledge of protein abundances in healthy tissues and their changes in disease is crucial for understanding biological processes in basic science and for the development of novel diagnostics and therapeutics. Mass spectrometrybased label-free protein quantification is used increasingly often to gain insights into physiological changes observed in perturbed systems. Although the soft ionization techniques electrospray ionization and matrix-assisted laser desorption/ionization have both been used for protein quantification, this article focuses on instrumental setups with a MALDI ion source. Beside reviewing current bioinformatic data-processing tools for label-free quantification and elaborating on the technical benefits of combining UHPLC and MALDI–MS, we outline the potential of state-of-the-art instruments by reporting unpublished results obtained from twenty-four complex biological samples. This review points out that the capabilities of LC–MALDI MS systems have not yet been fully utilized because of a lack of suitable software tools.
Online Abstract Figure
Graphical representation of the LC–MALDI–MS procedure for label-free protein quantification. Tryptic peptides are separated by reversed-phase ultra-high performance liquid chromatography and eluting fractions are mixed with matrix before robotic deposition on a MALDI target plate. Subsequent to analysis of each spot by MS
1
and MS
2
, bioinformatic tools are used for the label-free protein quantification</description><subject>Analytical Chemistry</subject><subject>Animals</subject><subject>Biochemistry</subject><subject>Bioinformatics</subject><subject>Biological</subject><subject>Characterization and Evaluation of Materials</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Computer programs</subject><subject>Food Science</subject><subject>Graphical representations</subject><subject>Humans</subject><subject>Ionization</subject><subject>Laboratory Medicine</subject><subject>Liquid chromatography</subject><subject>Monitoring/Environmental Analysis</subject><subject>Peptides</subject><subject>Proteins</subject><subject>Proteins - chemistry</subject><subject>Proteomics - methods</subject><subject>Proteomics - trends</subject><subject>Review</subject><subject>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - methods</subject><subject>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - trends</subject><issn>1618-2642</issn><issn>1618-2650</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkT1PwzAQhi0EolD4ASwoI0vAPjtOwlaVr0pFLCCxWY5zqVI1SetLkPrvST_oCEx30j3vO9zD2JXgt4Lz-I44B6FDLiCMEgnh-oidCS2SEHTEjw-7ggE7J5pzLqJE6FM2AJBRkqbpGfuc2gwXYeERg1Vn67YsSmfbsqmDjsp6FryOpg-ToLJEAS3Rtb6psPXr-8A1NZU5-i1Mga3zYIl-y5RfSBfspLALwsv9HLKPp8f38Us4fXuejEfT0CnB2xAKGacSLSI6gSIqUq0xyyKHWQIcUh7Hucp0JLVAK5PYucJxB5nUALrIQQ7Zza536ZtVh9SaqiSHi4WtsenIiFipWKQq_QcqpFYKEiX_RrmUOgHNN6jYoc43RB4Ls_RlZf26h8xGk9lpMr0ms9Fk1n3mel_fZRXmh8SPlx6AHUD9qZ6hN_Om83X_yF9avwGUkZ4e</recordid><startdate>20120901</startdate><enddate>20120901</enddate><creator>Benk, Amelie S.</creator><creator>Roesli, Christoph</creator><general>Springer-Verlag</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><scope>7QH</scope><scope>7UA</scope><scope>C1K</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20120901</creationdate><title>Label-free quantification using MALDI mass spectrometry: considerations and perspectives</title><author>Benk, Amelie S. ; Roesli, Christoph</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c410t-2f3793eaeeec1e15f966ebb5ceb82029077d4b65361ea387ccfc0c2b36226fd23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Analytical Chemistry</topic><topic>Animals</topic><topic>Biochemistry</topic><topic>Bioinformatics</topic><topic>Biological</topic><topic>Characterization and Evaluation of Materials</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Chromatography, High Pressure Liquid</topic><topic>Computer programs</topic><topic>Food Science</topic><topic>Graphical representations</topic><topic>Humans</topic><topic>Ionization</topic><topic>Laboratory Medicine</topic><topic>Liquid chromatography</topic><topic>Monitoring/Environmental Analysis</topic><topic>Peptides</topic><topic>Proteins</topic><topic>Proteins - chemistry</topic><topic>Proteomics - methods</topic><topic>Proteomics - trends</topic><topic>Review</topic><topic>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - methods</topic><topic>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - trends</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Benk, Amelie S.</creatorcontrib><creatorcontrib>Roesli, Christoph</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><collection>Aqualine</collection><collection>Water Resources Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Analytical and bioanalytical chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Benk, Amelie S.</au><au>Roesli, Christoph</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Label-free quantification using MALDI mass spectrometry: considerations and perspectives</atitle><jtitle>Analytical and bioanalytical chemistry</jtitle><stitle>Anal Bioanal Chem</stitle><addtitle>Anal Bioanal Chem</addtitle><date>2012-09-01</date><risdate>2012</risdate><volume>404</volume><issue>4</issue><spage>1039</spage><epage>1056</epage><pages>1039-1056</pages><issn>1618-2642</issn><eissn>1618-2650</eissn><abstract>Profound knowledge of protein abundances in healthy tissues and their changes in disease is crucial for understanding biological processes in basic science and for the development of novel diagnostics and therapeutics. Mass spectrometrybased label-free protein quantification is used increasingly often to gain insights into physiological changes observed in perturbed systems. Although the soft ionization techniques electrospray ionization and matrix-assisted laser desorption/ionization have both been used for protein quantification, this article focuses on instrumental setups with a MALDI ion source. Beside reviewing current bioinformatic data-processing tools for label-free quantification and elaborating on the technical benefits of combining UHPLC and MALDI–MS, we outline the potential of state-of-the-art instruments by reporting unpublished results obtained from twenty-four complex biological samples. This review points out that the capabilities of LC–MALDI MS systems have not yet been fully utilized because of a lack of suitable software tools.
Online Abstract Figure
Graphical representation of the LC–MALDI–MS procedure for label-free protein quantification. Tryptic peptides are separated by reversed-phase ultra-high performance liquid chromatography and eluting fractions are mixed with matrix before robotic deposition on a MALDI target plate. Subsequent to analysis of each spot by MS
1
and MS
2
, bioinformatic tools are used for the label-free protein quantification</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>22358999</pmid><doi>10.1007/s00216-012-5832-y</doi><tpages>18</tpages></addata></record> |
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subjects | Analytical Chemistry Animals Biochemistry Bioinformatics Biological Characterization and Evaluation of Materials Chemistry Chemistry and Materials Science Chromatography, High Pressure Liquid Computer programs Food Science Graphical representations Humans Ionization Laboratory Medicine Liquid chromatography Monitoring/Environmental Analysis Peptides Proteins Proteins - chemistry Proteomics - methods Proteomics - trends Review Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - methods Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization - trends |
title | Label-free quantification using MALDI mass spectrometry: considerations and perspectives |
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