Targeted metabolomics in cultured cells and tissues by mass spectrometry: Method development and validation
[Display omitted] •This study introduce a valid bioanalytical method for metabolic profiling.•The method validation and stability were studied carefully based on USFDA guidelines.•The targeted metabolomics method was tested on couple of biological systems cell lines and mouse tissue. Metabolomics is...
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Veröffentlicht in: | Analytica chimica acta 2014-10, Vol.845, p.53-61 |
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creator | Abdel Rahman, Anas M. Pawling, Judy Ryczko, Michael Caudy, Amy A. Dennis, James W. |
description | [Display omitted]
•This study introduce a valid bioanalytical method for metabolic profiling.•The method validation and stability were studied carefully based on USFDA guidelines.•The targeted metabolomics method was tested on couple of biological systems cell lines and mouse tissue.
Metabolomics is the identification and quantitation of small bio-molecules (metabolites) in biological samples under various environmental and genetic conditions. Mass spectrometry provides the unique opportunity for targeted identification and quantification of known metabolites by selective reaction monitoring (SRM). However, reproducibility of this approach depends on careful consideration of sample preparation, chemical classes, and stability of metabolites to be evaluated. Herein, we introduce and validate a targeted metabolite profiling workflow for cultured cells and tissues by liquid chromatography–triple quadrupole tandem mass spectrometry. The method requires a one-step extraction of water-soluble metabolites and targeted analysis of central metabolites that include glycolysis, amino acids, nucleotides, citric acid cycle, and the hexosamine biosynthetic pathway. The sensitivity, reproducibility and molecular stability of each targeted metabolite were assessed under experimental conditions. Quantitation of metabolites by peak area ratio was linear with a dilution over a 4 fold dynamic range with minimal deviation R2=0.98. Inter- and intra-day precision with cells and tissues had an average coefficient of variation |
doi_str_mv | 10.1016/j.aca.2014.06.012 |
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•This study introduce a valid bioanalytical method for metabolic profiling.•The method validation and stability were studied carefully based on USFDA guidelines.•The targeted metabolomics method was tested on couple of biological systems cell lines and mouse tissue.
Metabolomics is the identification and quantitation of small bio-molecules (metabolites) in biological samples under various environmental and genetic conditions. Mass spectrometry provides the unique opportunity for targeted identification and quantification of known metabolites by selective reaction monitoring (SRM). However, reproducibility of this approach depends on careful consideration of sample preparation, chemical classes, and stability of metabolites to be evaluated. Herein, we introduce and validate a targeted metabolite profiling workflow for cultured cells and tissues by liquid chromatography–triple quadrupole tandem mass spectrometry. The method requires a one-step extraction of water-soluble metabolites and targeted analysis of central metabolites that include glycolysis, amino acids, nucleotides, citric acid cycle, and the hexosamine biosynthetic pathway. The sensitivity, reproducibility and molecular stability of each targeted metabolite were assessed under experimental conditions. Quantitation of metabolites by peak area ratio was linear with a dilution over a 4 fold dynamic range with minimal deviation R2=0.98. Inter- and intra-day precision with cells and tissues had an average coefficient of variation <15% for cultured cell lines, and somewhat higher for mouse liver tissues. The method applied in triplicate measurements readily distinguished immortalized cells from malignant cells, as well as mouse littermates based on their hepatic metabolic profiles.</description><identifier>ISSN: 0003-2670</identifier><identifier>EISSN: 1873-4324</identifier><identifier>DOI: 10.1016/j.aca.2014.06.012</identifier><identifier>PMID: 25201272</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Amino acids ; Amino Acids - analysis ; Amino Acids - metabolism ; Animals ; Biological ; Cells, Cultured ; Citric Acid - analysis ; Citric Acid - metabolism ; Citric Acid Cycle ; Deviation ; Diagnostics ; Extraction ; HEK293 Cells ; HeLa Cells ; Hexosamines - analysis ; Hexosamines - biosynthesis ; Humans ; Mass Spectrometry ; Metabolism ; Metabolites ; Metabolomics - methods ; Mice ; Nucleotides - analysis ; Nucleotides - metabolism ; Precision ; Reproducibility ; Sensitivity ; Stability</subject><ispartof>Analytica chimica acta, 2014-10, Vol.845, p.53-61</ispartof><rights>2014</rights><rights>Copyright © 2014. Published by Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c555t-2cb8bf5ab148da054e552b99f779003894320ad1a12d2f5923afe5363dcf9a633</citedby><cites>FETCH-LOGICAL-c555t-2cb8bf5ab148da054e552b99f779003894320ad1a12d2f5923afe5363dcf9a633</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0003267014007259$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25201272$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Abdel Rahman, Anas M.</creatorcontrib><creatorcontrib>Pawling, Judy</creatorcontrib><creatorcontrib>Ryczko, Michael</creatorcontrib><creatorcontrib>Caudy, Amy A.</creatorcontrib><creatorcontrib>Dennis, James W.</creatorcontrib><title>Targeted metabolomics in cultured cells and tissues by mass spectrometry: Method development and validation</title><title>Analytica chimica acta</title><addtitle>Anal Chim Acta</addtitle><description>[Display omitted]
•This study introduce a valid bioanalytical method for metabolic profiling.•The method validation and stability were studied carefully based on USFDA guidelines.•The targeted metabolomics method was tested on couple of biological systems cell lines and mouse tissue.
Metabolomics is the identification and quantitation of small bio-molecules (metabolites) in biological samples under various environmental and genetic conditions. Mass spectrometry provides the unique opportunity for targeted identification and quantification of known metabolites by selective reaction monitoring (SRM). However, reproducibility of this approach depends on careful consideration of sample preparation, chemical classes, and stability of metabolites to be evaluated. Herein, we introduce and validate a targeted metabolite profiling workflow for cultured cells and tissues by liquid chromatography–triple quadrupole tandem mass spectrometry. The method requires a one-step extraction of water-soluble metabolites and targeted analysis of central metabolites that include glycolysis, amino acids, nucleotides, citric acid cycle, and the hexosamine biosynthetic pathway. The sensitivity, reproducibility and molecular stability of each targeted metabolite were assessed under experimental conditions. Quantitation of metabolites by peak area ratio was linear with a dilution over a 4 fold dynamic range with minimal deviation R2=0.98. Inter- and intra-day precision with cells and tissues had an average coefficient of variation <15% for cultured cell lines, and somewhat higher for mouse liver tissues. The method applied in triplicate measurements readily distinguished immortalized cells from malignant cells, as well as mouse littermates based on their hepatic metabolic profiles.</description><subject>Amino acids</subject><subject>Amino Acids - analysis</subject><subject>Amino Acids - metabolism</subject><subject>Animals</subject><subject>Biological</subject><subject>Cells, Cultured</subject><subject>Citric Acid - analysis</subject><subject>Citric Acid - metabolism</subject><subject>Citric Acid Cycle</subject><subject>Deviation</subject><subject>Diagnostics</subject><subject>Extraction</subject><subject>HEK293 Cells</subject><subject>HeLa Cells</subject><subject>Hexosamines - analysis</subject><subject>Hexosamines - biosynthesis</subject><subject>Humans</subject><subject>Mass Spectrometry</subject><subject>Metabolism</subject><subject>Metabolites</subject><subject>Metabolomics - methods</subject><subject>Mice</subject><subject>Nucleotides - analysis</subject><subject>Nucleotides - metabolism</subject><subject>Precision</subject><subject>Reproducibility</subject><subject>Sensitivity</subject><subject>Stability</subject><issn>0003-2670</issn><issn>1873-4324</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc1u1DAURq0K1E4LD8AGeckmwT-xk8AKVUCRitiUtXVj34CHJB5sZ6R5-3qYwpJ2ZVk-35W_ewh5xVnNGddvtzVYqAXjTc10zbg4IxvetbJqpGiekQ1jTFZCt-yCXKa0LVfBWXNOLoQqIdGKDfl1B_EHZnR0xgxDmMLsbaJ-oXad8hrLg8VpShQWR7NPacVEhwOdISWadmhzDCUZD-_oV8w_g6MO9ziF3YxL_hPaw-QdZB-WF-T5CFPClw_nFfn-6ePd9U11--3zl-sPt5VVSuVK2KEbRgUDbzoHTDWolBj6fmzbvhTq-tKOgePAhROj6oWEEZXU0tmxBy3lFXlzmruL4Xf5bzazT8cWsGBYk-G67cr6OqWfgIpeqk62_eOo0pyLTqqmoPyE2hhSijiaXfQzxIPhzBzNma0p5szRnGHaFBcl8_ph_DrM6P4l_qoqwPsTgGV1e4_RJOtxseh8LBqMC_4_4-8BsTapDw</recordid><startdate>20141003</startdate><enddate>20141003</enddate><creator>Abdel Rahman, Anas M.</creator><creator>Pawling, Judy</creator><creator>Ryczko, Michael</creator><creator>Caudy, Amy A.</creator><creator>Dennis, James W.</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><scope>7QH</scope><scope>7UA</scope><scope>C1K</scope><scope>7U5</scope><scope>8FD</scope><scope>L7M</scope></search><sort><creationdate>20141003</creationdate><title>Targeted metabolomics in cultured cells and tissues by mass spectrometry: Method development and validation</title><author>Abdel Rahman, Anas M. ; Pawling, Judy ; Ryczko, Michael ; Caudy, Amy A. ; Dennis, James W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c555t-2cb8bf5ab148da054e552b99f779003894320ad1a12d2f5923afe5363dcf9a633</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Amino acids</topic><topic>Amino Acids - analysis</topic><topic>Amino Acids - metabolism</topic><topic>Animals</topic><topic>Biological</topic><topic>Cells, Cultured</topic><topic>Citric Acid - analysis</topic><topic>Citric Acid - metabolism</topic><topic>Citric Acid Cycle</topic><topic>Deviation</topic><topic>Diagnostics</topic><topic>Extraction</topic><topic>HEK293 Cells</topic><topic>HeLa Cells</topic><topic>Hexosamines - analysis</topic><topic>Hexosamines - biosynthesis</topic><topic>Humans</topic><topic>Mass Spectrometry</topic><topic>Metabolism</topic><topic>Metabolites</topic><topic>Metabolomics - methods</topic><topic>Mice</topic><topic>Nucleotides - analysis</topic><topic>Nucleotides - metabolism</topic><topic>Precision</topic><topic>Reproducibility</topic><topic>Sensitivity</topic><topic>Stability</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Abdel Rahman, Anas M.</creatorcontrib><creatorcontrib>Pawling, Judy</creatorcontrib><creatorcontrib>Ryczko, Michael</creatorcontrib><creatorcontrib>Caudy, Amy A.</creatorcontrib><creatorcontrib>Dennis, James W.</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>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Analytica chimica acta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Abdel Rahman, Anas M.</au><au>Pawling, Judy</au><au>Ryczko, Michael</au><au>Caudy, Amy A.</au><au>Dennis, James W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Targeted metabolomics in cultured cells and tissues by mass spectrometry: Method development and validation</atitle><jtitle>Analytica chimica acta</jtitle><addtitle>Anal Chim Acta</addtitle><date>2014-10-03</date><risdate>2014</risdate><volume>845</volume><spage>53</spage><epage>61</epage><pages>53-61</pages><issn>0003-2670</issn><eissn>1873-4324</eissn><abstract>[Display omitted]
•This study introduce a valid bioanalytical method for metabolic profiling.•The method validation and stability were studied carefully based on USFDA guidelines.•The targeted metabolomics method was tested on couple of biological systems cell lines and mouse tissue.
Metabolomics is the identification and quantitation of small bio-molecules (metabolites) in biological samples under various environmental and genetic conditions. Mass spectrometry provides the unique opportunity for targeted identification and quantification of known metabolites by selective reaction monitoring (SRM). However, reproducibility of this approach depends on careful consideration of sample preparation, chemical classes, and stability of metabolites to be evaluated. Herein, we introduce and validate a targeted metabolite profiling workflow for cultured cells and tissues by liquid chromatography–triple quadrupole tandem mass spectrometry. The method requires a one-step extraction of water-soluble metabolites and targeted analysis of central metabolites that include glycolysis, amino acids, nucleotides, citric acid cycle, and the hexosamine biosynthetic pathway. The sensitivity, reproducibility and molecular stability of each targeted metabolite were assessed under experimental conditions. Quantitation of metabolites by peak area ratio was linear with a dilution over a 4 fold dynamic range with minimal deviation R2=0.98. Inter- and intra-day precision with cells and tissues had an average coefficient of variation <15% for cultured cell lines, and somewhat higher for mouse liver tissues. The method applied in triplicate measurements readily distinguished immortalized cells from malignant cells, as well as mouse littermates based on their hepatic metabolic profiles.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>25201272</pmid><doi>10.1016/j.aca.2014.06.012</doi><tpages>9</tpages></addata></record> |
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subjects | Amino acids Amino Acids - analysis Amino Acids - metabolism Animals Biological Cells, Cultured Citric Acid - analysis Citric Acid - metabolism Citric Acid Cycle Deviation Diagnostics Extraction HEK293 Cells HeLa Cells Hexosamines - analysis Hexosamines - biosynthesis Humans Mass Spectrometry Metabolism Metabolites Metabolomics - methods Mice Nucleotides - analysis Nucleotides - metabolism Precision Reproducibility Sensitivity Stability |
title | Targeted metabolomics in cultured cells and tissues by mass spectrometry: Method development and validation |
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