Challenges in mass spectrometry-based proteomics

被引:119
作者
Reinders, J [1 ]
Lewandrowski, U [1 ]
Moebius, J [1 ]
Wagner, Y [1 ]
Sickmann, A [1 ]
机构
[1] Univ Wurzburg, Rudolf Virchow Ctr Expt Biomed, Prot Mass Spectrometry & Funct Proteom Grp, D-97078 Wurzburg, Germany
关键词
de novo sequencing; organelle analysis; post-translational modifications; quantification; review;
D O I
10.1002/pmic.200400869
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
During the last decade, protein analysis and proteomics have been established as new tools for understanding various biological problems. As the identification of proteins after classical separation techniques, such as two-dimensional gel electrophoresis, have become standard methods, new challenges arise in the field of proteomics. The development of "functional proteomics" combines functional characterization, like regulation, localization and modification, with the identification of proteins for deeper insight into cellular functions. Therefore, different mass spectrometric techniques for the analysis of post-translational modifications, such as phosphorylation and glycosylation, have been established as well as isolation and separation methods for the analysis of highly complex samples, e.g. protein complexes or cell organelles. Furthermore, quantification of protein levels within cells is becoming a focus of interest as mass spectrometric methods for relative or even absolute quantification have currently not been available.
引用
收藏
页码:3686 / 3703
页数:18
相关论文
共 125 条
[1]   Mass spectrometry-based proteomics [J].
Aebersold, R ;
Mann, M .
NATURE, 2003, 422 (6928) :198-207
[2]   Phosphopeptide analysis by matrix-assisted laser desorption time-of-flight mass spectrometry [J].
Annan, RS ;
Carr, SA .
ANALYTICAL CHEMISTRY, 1996, 68 (19) :3413-3421
[3]   On the frequency of protein glycosylation, as deduced from analysis of the SWISS-PROT database [J].
Apweiler, R ;
Hermjakob, H ;
Sharon, N .
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS, 1999, 1473 (01) :4-8
[4]   Affinity purification-mass spectrometry - Powerful tools for the characterization of protein complexes [J].
Bauer, A ;
Kuster, B .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2003, 270 (04) :570-578
[5]   MASS-SPECTROMETRY OF PEPTIDES AND PROTEINS [J].
BIEMANN, K .
ANNUAL REVIEW OF BIOCHEMISTRY, 1992, 61 :977-1010
[6]   Cell biologists sort things out: analysis and purification of intracellular organelles by flow cytometry [J].
Bock, I ;
Steinlein, P ;
Huber, LA .
TRENDS IN CELL BIOLOGY, 1997, 7 (12) :499-503
[7]   Gaining insight into a complex organelle, the phagosome, using two-dimensional gel electrophoresis [J].
Burkhardt, J ;
Huber, LA ;
Dieplinger, H ;
Blocker, A ;
Griffiths, G ;
Desjardins, M .
ELECTROPHORESIS, 1995, 16 (12) :2249-2257
[8]   De novo peptide sequencing and quantitative profiling of complex protein mixtures using mass-coded abundance tagging [J].
Cagney, G ;
Emili, A .
NATURE BIOTECHNOLOGY, 2002, 20 (02) :163-170
[9]  
CARLSON DM, 1968, J BIOL CHEM, V243, P616
[10]   On the detailed mechanisms of collision-induced dissociation experiments performed by electrospray ion trap [J].
Catinella, S ;
Pelizzi, N ;
Barboso, S ;
Favretto, D ;
Seraglia, R ;
Traldi, P .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2002, 16 (20) :1897-1902