Proteome profiling for assessing diversity:: Analysis of individual heads of Drosophila melanogaster using LC-ion mobility-MS

被引:34
作者
Taraszka, JA [1 ]
Gao, XF
Valentine, SJ
Sowell, RA
Koeniger, SL
Miller, DF
Kaufman, TC
Clemmer, DE
机构
[1] Indiana Univ, Dept Chem, Bloomington, IN 47405 USA
[2] Indiana Univ, Dept Biol, Bloomington, IN 47405 USA
[3] Novartis Inst Biomed Res Inc, Cambridge, MA 02139 USA
关键词
Drosophila melanogaster; ion mobility; mass spectrometry; proteomics;
D O I
10.1021/pr050037o
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The proteomes of three heads of individual Drosophila melanogaster organisms have been analyzed and compared by a combination of liquid chromatography, ion mobility spectrometry, and mass spectrometry approaches. In total, 197 proteins are identified among all three individuals (an average of 120 +/- 20 proteins per individual), of which at least 101 proteins are present in all three individuals. Within all three datasets, more than 25 000 molecular ions (an average of 9000 +/- 2000 per individual) corresponding to protonated precursor ions of individual peptides have been observed. A comparison of peaks among the datasets reveals that peaks corresponding to protonated pepticles that are found in all heads are more intense than those features that appear between pairs of or within only one of the individuals. Moreover, there is little variability in the relative intensities of the peaks common among all individuals. It appears that it is the lower abundance components of the proteome that play the most significant role in determining unique features of individuals.
引用
收藏
页码:1238 / 1247
页数:10
相关论文
共 58 条
[1]   Mass spectrometry-based proteomics [J].
Aebersold, R ;
Mann, M .
NATURE, 2003, 422 (6928) :198-207
[2]   Separation and identification of some chemical warfare degradation products using electrospray high resolution ion mobility spectrometry with mass selected detection [J].
Asbury, GR ;
Wu, C ;
Siems, WF ;
Hill, HH .
ANALYTICA CHIMICA ACTA, 2000, 404 (02) :273-283
[3]   Gene Ontology: tool for the unification of biology [J].
Ashburner, M ;
Ball, CA ;
Blake, JA ;
Botstein, D ;
Butler, H ;
Cherry, JM ;
Davis, AP ;
Dolinski, K ;
Dwight, SS ;
Eppig, JT ;
Harris, MA ;
Hill, DP ;
Issel-Tarver, L ;
Kasarskis, A ;
Lewis, S ;
Matese, JC ;
Richardson, JE ;
Ringwald, M ;
Rubin, GM ;
Sherlock, G .
NATURE GENETICS, 2000, 25 (01) :25-29
[4]   Regulation of alternative replication bypass pathways at stalled replication forks and its effects on genome stability: a yeast model [J].
Barbour, L ;
Xiao, W .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2003, 532 (1-2) :137-155
[5]  
BENEDICTE M, 2000, TRENDS BIOCHEM SCI, V25, P173
[6]   Protein diversity from alternative splicing: A challenge for bioinformatics and post-genome biology [J].
Black, DL .
CELL, 2000, 103 (03) :367-370
[7]   Mechanisms of alternative pre-messenger RNA splicing [J].
Black, DL .
ANNUAL REVIEW OF BIOCHEMISTRY, 2003, 72 :291-336
[8]   C-to-U RNA editing: Mechanisms leading to genetic diversity [J].
Blanc, V ;
Davidson, NO .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (03) :1395-1398
[9]   Separation of spin-orbit coupled metastable states of Kr+ and Xe+ by ion mobility [J].
Bluhm, BK ;
North, SW ;
Russell, DH .
JOURNAL OF CHEMICAL PHYSICS, 2001, 114 (04) :1709-1715
[10]   GAS-PHASE ION CHROMATOGRAPHY - TRANSITION-METAL STATE SELECTION AND CARBON CLUSTER FORMATION [J].
BOWERS, MT ;
KEMPER, PR ;
VON HELDEN, G ;
VANKOPPEN, PAM .
SCIENCE, 1993, 260 (5113) :1446-1451