Rapid Assessment of RNAi-mediated Protein Depletion by Selected Reaction Monitoring Mass Spectrometry
We describe the use of a targeted proteomics approach, selected reaction monitoring (SRM) mass spectrometry, to detect and assess RNAi-mediated depletion or “knockdown” of specific proteins from human cells and from Drosophila flies. This label-free approach does not require any specific reagents to...
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Veröffentlicht in: | Journal of proteome research 2013-07, Vol.12 (7), p.3246-3254 |
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creator | Glukhova, Veronika A Tomazela, Daniela M Findlay, Geoffrey D Monnat, Raymond J MacCoss, Michael J |
description | We describe the use of a targeted proteomics approach, selected reaction monitoring (SRM) mass spectrometry, to detect and assess RNAi-mediated depletion or “knockdown” of specific proteins from human cells and from Drosophila flies. This label-free approach does not require any specific reagents to confirm the depletion of RNAi target protein(s) in unfractionated cell or whole organism extracts. The protocol described here is general, can be developed rapidly, and can be multiplexed to detect and measure multiple proteins at once. Furthermore, the methodology can be extended to any tandem mass spectrometer, making it widely accessible. This methodology will be applicable to a wide range of basic science and clinical questions where RNAi-mediated protein depletion needs to be verified, or where differences in relative abundance of target proteins need to be rapidly assessed between samples. |
doi_str_mv | 10.1021/pr400067k |
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Proteome Res</addtitle><description>We describe the use of a targeted proteomics approach, selected reaction monitoring (SRM) mass spectrometry, to detect and assess RNAi-mediated depletion or “knockdown” of specific proteins from human cells and from Drosophila flies. This label-free approach does not require any specific reagents to confirm the depletion of RNAi target protein(s) in unfractionated cell or whole organism extracts. The protocol described here is general, can be developed rapidly, and can be multiplexed to detect and measure multiple proteins at once. Furthermore, the methodology can be extended to any tandem mass spectrometer, making it widely accessible. This methodology will be applicable to a wide range of basic science and clinical questions where RNAi-mediated protein depletion needs to be verified, or where differences in relative abundance of target proteins need to be rapidly assessed between samples.</description><subject>Animals</subject><subject>Cell Line</subject><subject>Drosophila</subject><subject>Gene Knockdown Techniques</subject><subject>Humans</subject><subject>mass spectrometry</subject><subject>monitoring</subject><subject>Peptide Fragments - chemistry</subject><subject>Peptide Fragments - genetics</subject><subject>protein depletion</subject><subject>proteins</subject><subject>Proteins - genetics</subject><subject>Proteins - isolation & purification</subject><subject>proteome</subject><subject>proteomics</subject><subject>Proteomics - methods</subject><subject>rapid methods</subject><subject>RNA Interference</subject><subject>spectrometers</subject><subject>Tandem Mass Spectrometry</subject><issn>1535-3893</issn><issn>1535-3907</issn><issn>1535-3907</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU9v1DAQxa2Kqi2FA18A-YIEh4DtiePkgrTqP5BaQFs4W449Lm6TONhZpP32Tdl21UqVOM1o5qenefMIecPZR84E_zSmkjFWqZsdcsAlyAIapl489HUD--RlzteMcakY7JF9AYpDDfyA4NKMwdFFzphzj8NEo6fLb4tQ9OiCmdDRHylOGAZ6jGOHU4gDbdf0Eju0d9slGvtveBGHMMUUhit6YXKml-MMpNjjlNavyK43XcbX9_WQ_Do9-Xn0pTj_fvb1aHFemBLqqSiNceC5scgrZhkIJ4yvfaO8bIWXdSkq50VbGe8aK4RySjopS2hb26CoEA7J543uuGrn--3sJ5lOjyn0Jq11NEE_3Qzht76KfzWoSpVCzALv7wVS_LPCPOk-ZItdZwaMq6wFk1ArVfH_oxyaugQpQc3ohw1qU8w5od9exJm-S1BvE5zZt48tbMmHyGbg3QYwNuvruErD_NFnhG4BoOqkrA</recordid><startdate>20130705</startdate><enddate>20130705</enddate><creator>Glukhova, Veronika A</creator><creator>Tomazela, Daniela M</creator><creator>Findlay, Geoffrey D</creator><creator>Monnat, Raymond J</creator><creator>MacCoss, Michael J</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><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope></search><sort><creationdate>20130705</creationdate><title>Rapid Assessment of RNAi-mediated Protein Depletion by Selected Reaction Monitoring Mass Spectrometry</title><author>Glukhova, Veronika A ; Tomazela, Daniela M ; Findlay, Geoffrey D ; Monnat, Raymond J ; MacCoss, Michael J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a438t-4aad3f1ace160c032d2af8f97f5b2f58426df2b6afd9c227d75d5543bbc9e26e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Animals</topic><topic>Cell Line</topic><topic>Drosophila</topic><topic>Gene Knockdown Techniques</topic><topic>Humans</topic><topic>mass spectrometry</topic><topic>monitoring</topic><topic>Peptide Fragments - chemistry</topic><topic>Peptide Fragments - genetics</topic><topic>protein depletion</topic><topic>proteins</topic><topic>Proteins - genetics</topic><topic>Proteins - isolation & purification</topic><topic>proteome</topic><topic>proteomics</topic><topic>Proteomics - methods</topic><topic>rapid methods</topic><topic>RNA Interference</topic><topic>spectrometers</topic><topic>Tandem Mass Spectrometry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Glukhova, Veronika A</creatorcontrib><creatorcontrib>Tomazela, Daniela M</creatorcontrib><creatorcontrib>Findlay, Geoffrey D</creatorcontrib><creatorcontrib>Monnat, Raymond J</creatorcontrib><creatorcontrib>MacCoss, Michael J</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>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of proteome research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Glukhova, Veronika A</au><au>Tomazela, Daniela M</au><au>Findlay, Geoffrey D</au><au>Monnat, Raymond J</au><au>MacCoss, Michael J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rapid Assessment of RNAi-mediated Protein Depletion by Selected Reaction Monitoring Mass Spectrometry</atitle><jtitle>Journal of proteome research</jtitle><addtitle>J. Proteome Res</addtitle><date>2013-07-05</date><risdate>2013</risdate><volume>12</volume><issue>7</issue><spage>3246</spage><epage>3254</epage><pages>3246-3254</pages><issn>1535-3893</issn><issn>1535-3907</issn><eissn>1535-3907</eissn><abstract>We describe the use of a targeted proteomics approach, selected reaction monitoring (SRM) mass spectrometry, to detect and assess RNAi-mediated depletion or “knockdown” of specific proteins from human cells and from Drosophila flies. This label-free approach does not require any specific reagents to confirm the depletion of RNAi target protein(s) in unfractionated cell or whole organism extracts. The protocol described here is general, can be developed rapidly, and can be multiplexed to detect and measure multiple proteins at once. Furthermore, the methodology can be extended to any tandem mass spectrometer, making it widely accessible. 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subjects | Animals Cell Line Drosophila Gene Knockdown Techniques Humans mass spectrometry monitoring Peptide Fragments - chemistry Peptide Fragments - genetics protein depletion proteins Proteins - genetics Proteins - isolation & purification proteome proteomics Proteomics - methods rapid methods RNA Interference spectrometers Tandem Mass Spectrometry |
title | Rapid Assessment of RNAi-mediated Protein Depletion by Selected Reaction Monitoring Mass Spectrometry |
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