Plant proteome analysis by mass spectrometry: principles, problems, pitfalls and recent developments
Basic strategy from extraction through fractionation and purification to mass spectrometric analysis is discussed and some plant proteomic applications are reviewed, as are imminent future developments in relevant mass spectrometric instrumentation. The genome of several species has now been elucida...
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Published in | Phytochemistry Vol. 65; no. 11; pp. 1449 - 1485 |
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Main Authors | , , , |
Format | Book Review Journal Article |
Language | English |
Published |
England
Elsevier Ltd
01.06.2004
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Abstract | Basic strategy from extraction through fractionation and purification to mass spectrometric analysis is discussed and some plant proteomic applications are reviewed, as are imminent future developments in relevant mass spectrometric instrumentation.
The genome of several species has now been elucidated; these genomes indicate the proteomic potential of the cell. While identification of genomes has been, and continues to be, a technically and intellectually demanding process, the identification of the proteome contains inherently greater difficulties. The proteome of each living cell is dynamic, altering in response to the individual cell's metabolic state and reception of intracellular and extracellular signal molecules, and many of the proteins which are expressed will be post-translationally altered. Thus if the purpose of the proteome analysis is to aid the understanding of protein function and interaction, then it is identification of the proteins in their final state which is required: for this mass spectrometric identification of individual proteins, indicating site and nature of modifications, is essential. Here we review the principles of the methodologies involved in such analyses, give some indication of current achievements in plant proteomics, and indicate imminent and prospective technical developments. |
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AbstractList | The genome of several species has now been elucidated; these genomes indicate the proteomic potential of the cell. While identification of genomes has been, and continues to be, a technically and intellectually demanding process, the identification of the proteome contains inherently greater difficulties. The proteome of each living cell is dynamic, altering in response to the individual cell's metabolic state and reception of intracellular and extracellular signal molecules, and many of the proteins which are expressed will be post-translationally altered. Thus if the purpose of the proteome analysis is to aid the understanding of protein function and interaction, then it is identification of the proteins in their final state which is required: for this mass spectrometric identification of individual proteins, indicating site and nature of modifications, is essential. Here we review the principles of the methodologies involved in such analyses, give some indication of current achievements in plant proteomics, and indicate imminent and prospective technical developments. Basic strategy from extraction through fractionation and purification to mass spectrometric analysis is discussed and some plant proteomic applications are reviewed, as are imminent future developments in relevant mass spectrometric instrumentation. The genome of several species has now been elucidated; these genomes indicate the proteomic potential of the cell. While identification of genomes has been, and continues to be, a technically and intellectually demanding process, the identification of the proteome contains inherently greater difficulties. The proteome of each living cell is dynamic, altering in response to the individual cell's metabolic state and reception of intracellular and extracellular signal molecules, and many of the proteins which are expressed will be post-translationally altered. Thus if the purpose of the proteome analysis is to aid the understanding of protein function and interaction, then it is identification of the proteins in their final state which is required: for this mass spectrometric identification of individual proteins, indicating site and nature of modifications, is essential. Here we review the principles of the methodologies involved in such analyses, give some indication of current achievements in plant proteomics, and indicate imminent and prospective technical developments. |
Author | Brenton, A.Gareth Dudley, Edward Smith, Chris J. Newton, Russell P. |
Author_xml | – sequence: 1 givenname: Russell P. surname: Newton fullname: Newton, Russell P. email: r.p.newton@swansea.ac.uk organization: Biochemistry Group, School of Biological Sciences, University of Wales Swansea, Wallace Building, Singleton Park, Swansea SA2 8PP, UK – sequence: 2 givenname: A.Gareth surname: Brenton fullname: Brenton, A.Gareth organization: Mass Spectrometry Research Unit, Department of Chemistry, Grove Building, University of Wales Swansea, Singleton Park, Swansea SA2 8PP, UK – sequence: 3 givenname: Chris J. surname: Smith fullname: Smith, Chris J. organization: Biochemistry Group, School of Biological Sciences, University of Wales Swansea, Wallace Building, Singleton Park, Swansea SA2 8PP, UK – sequence: 4 givenname: Edward surname: Dudley fullname: Dudley, Edward organization: Biomolecular Analysis Mass Spectrometry (BAMS) Facility, Grove Building, University of Wales Swansea, Singleton Park, Swansea SA2 8PP, UK |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/15276445$$D View this record in MEDLINE/PubMed |
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Available from Aebersold (BIB1) 2003; 14 Hale, Butler, Knierman, Becker (BIB72) 2000; 287 Andon, Hollongworth, Koller, Greenland, Yates, Haynes (BIB2) 2002; 2 Yu, Hu, Wang, Wong, Li, Liu, Deng, Dai, Zhou, Zhang, Cao, Liu, Sun, Tang, Chen, Huang, Lin, Ye, Tong, Cong, Geng, Han, Li, Li, Hu, Huang, Li, Li, Liu, Li, Liu, Qi, Liu, Li, Li, Wang, Lu, Wu, Zhu, Ni, Han, Dong, Ren, Feng, Cui, Li, Wang, Xu, Zhai, Xu, Zhang, He, Zhang, Xu, Zhang, Zheng, Dong, Zeng, Tao, Ye, Tan, Ren, Chen, He, Liu, Tian, Tian, Xia, Bao, Li, Gao, Cao, Wang, Zhao, Li, Chen, Wang, Zhang, Hu, Wang, Liu, Yang, Zhang, Xiong, Li, Mao, Zhou, Zhu, Chen, Hao, Zheng, Chen, Guo, Li, Liu, Tao, Wang, Zhu, Yuan, Yang (BIB202) 2002; 296 Ells, Froese, Hrudey, Purves, Guevremont, Barnett (BIB48) 2000; 14 Lee, Yi, Wen, Reily, Pohl, Nelson, Aebersold, Goodlett (BIB101) 2003; 803 Gomez, Bil, Aguilera, Nishio, Faull, Whitelegge (BIB65) 2003; 2 Komatsu, Konishi, Shen, Yang (BIB94) 2003; 2 Koo, Ohirogge (BIB95) 2002; 130 Schnaible, Wefing, Resemann, Suckau, Bu1cker, Wolf-Ku1mmeth, Hoffmann (BIB152) 2002; 74 Wasinger, Cordwell, Cerpapoljak, Yan, Gooley, Wilkins, Duncan, Harris, Humphrey-Smith (BIB185) 1995; 16 Chivas, Ndimba, Simon, Robertson, Yu, Knox, Bolwell, Slabas (BIB32) 2002; 23 Peck, Nuhse, Hess, Iglesias, Meins, Boller (BIB134) 2001; 13 Gaberc-Porekar, Menart (BIB56) 2001; 49 Mackun, Downard (BIB113) 2003; 318 Stroebel, Choquet, Popot, Picot (BIB168) 2003; 426 Chapman (BIB30) 2000; vol. 146 Sonksen, C.P., Roepstorff, P., Markgren, P.O., Danielson, U.H., Hamalainen, M.D., Jansson, O., 2001. Capture and analysis of low molecular weight ligands by surface Nedelkov, Nelson (BIB129) 2001; 16 Kubis, Baldwin, Patel, Razzaq, Dupree, Lilley, Kurth, Leister, Jarvis (BIB97) 2003; 15 Sweetlove, Heazlewood, Herald, Holtzapffel, Day, Leaver, Millar (BIB169) 2002; 32 Wagner, Sickmann, Meyer, Daum (BIB179) 2003; 14 Leister (BIB104) 2003; 19 Figeys (BIB53) 2003; 75 Morris, Paxton, Dell, Langhorne, Berg, Bordoli, Hoyes, Bateman (BIB126) 1996; 10 Wolff, Eckers, Sage, Giles, Bateman (BIB194) 2001; 73 Sobott, Hernandez, McCammon, Tito, Robinson (BIB164) 2002; 74 Yao, Freas, Ramirez, Demirev, Fenselau (BIB201) 2001; 73 Gallardo, Job, Groot, Puype, Demol, Vandekerckhove, Job (BIB57) 2001; 126 Heazlewood, Whelan, Millar (BIB78) 2003; 540 Maltman, Simon, Wheeler, Dunn, Wait, Slabas (BIB115) 2002; 23 Wu, Yates (BIB197) 2003 Kalume, Molina, Pandey (BIB89) 2003; 7 Xu, Caprioli (BIB199) 2002; 13 Gluckmann, Pfenninger, Kruger, Thierolf, Karas, Horneffer, Hillenkamp, Strupat (BIB62) 2001; 210/211 Shen, Sharma, Komatsu (BIB160) 2003; 26 Zhu, Bilgin, Snyder (BIB206) 2003; 72 Calikowski, Meulia, Meier (BIB21) 2003; 90 Schleiff, Eichacker, Eckart, Becker, Mirus, Stahl, Soll (BIB151) 2003; 12 Haslam, Downie, Raveton, Gallardo, Job, Pallett, John, Parry, Coleman (BIB76) 2003; 143 Laiko, Moyer, Cotter (BIB98) 2000; 72 Borner, Lilley, Stevens, Dupree (BIB15) 2003; 132 Seigneurin-Berny, Rolland, Garin, Joyard (BIB156) 1999; 19 Zivy, de Vienne (BIB207) 2000; 44 Jansen, Nap, Mylnarova (BIB86) 2002; 20 Schwartz, Reyzer, Caprioli (BIB154) 2003; 38 Skylas, Copeland, Rathmell, Wrigley (BIB163) 2001; 1 Chakraborty, Regnier (BIB25) 2002; 949 Chapman (BIB31) 2002; 30 Thiellement, Zivy, Plomion (BIB173) 2002; 782 Liu, Berger, Chakraborty, Plumb, Cohen (BIB111) 2002; 782 Butt, Lum, Lo (BIB19) 2001; 216 Froelich, Wilkerson, Ray, McAndrews, Osteryoung, Gage, Phinney (BIB54) 2003; 2 Lilley, Razzaq, Dupree (BIB106) 2001; 6 Rossignol (BIB147) 2001; 12 Whitelegge, Gunderson, Faull (BIB189) 1998; 7 Walker (BIB181) 2002 Applied Biosystems, 2002. Achieving reliable protein quantitation results using ICAT reagents, MALDI-TOF Laiko (10.1016/j.phytochem.2004.04.015_BIB98) 2000; 72 Lilley (10.1016/j.phytochem.2004.04.015_BIB106) 2001; 6 McPherson (10.1016/j.phytochem.2004.04.015_BIB121) 2001; 409 Zhang (10.1016/j.phytochem.2004.04.015_BIB204) 2000; 72 Peltier (10.1016/j.phytochem.2004.04.015_BIB137) 2001; 276 Davis (10.1016/j.phytochem.2004.04.015_BIB41) 1997; 8 Schnaible (10.1016/j.phytochem.2004.04.015_BIB152) 2002; 74 Mo (10.1016/j.phytochem.2004.04.015_BIB125) 2003; 21 Link (10.1016/j.phytochem.2004.04.015_BIB108) 1995; vol. 112 Rabilloud (10.1016/j.phytochem.2004.04.015_BIB142) 2002; 2 Salekdeh (10.1016/j.phytochem.2004.04.015_BIB148) 2002; 2 Thiellement (10.1016/j.phytochem.2004.04.015_BIB173) 2002; 782 Borner (10.1016/j.phytochem.2004.04.015_BIB15) 2003; 132 Black (10.1016/j.phytochem.2004.04.015_BIB11) 2003; 72 Rejtar (10.1016/j.phytochem.2004.04.015_BIB145) 2002; 1 Walker (10.1016/j.phytochem.2004.04.015_BIB181) 2002 Hoaglund-Hyzer (10.1016/j.phytochem.2004.04.015_BIB80) 2001; 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Snippet | Basic strategy from extraction through fractionation and purification to mass spectrometric analysis is discussed and some plant proteomic applications are... The genome of several species has now been elucidated; these genomes indicate the proteomic potential of the cell. While identification of genomes has been,... |
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SubjectTerms | chemical analysis chloroplasts electrospray tandem mass spectrometry literature reviews mass spectrometry Mass Spectrometry - instrumentation Mass Spectrometry - methods Mass Spectrometry - trends matrix-assisted laser desorption ionisation-time-of-flight mass spectrometry mitochondria Models, Molecular organelles plant extracts plant proteins Plant Proteins - analysis Plants - genetics Plants - metabolism polyacrylamide gel electrophoresis post-translational modification protein-protein interactions proteome Proteome - analysis proteomics Proteomics - methods Spectrometry, Mass, Electrospray Ionization Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization |
Title | Plant proteome analysis by mass spectrometry: principles, problems, pitfalls and recent developments |
URI | https://dx.doi.org/10.1016/j.phytochem.2004.04.015 https://www.ncbi.nlm.nih.gov/pubmed/15276445 https://search.proquest.com/docview/17821595 https://search.proquest.com/docview/66750539 |
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