Relative Abundance of Integral Plasma Membrane Proteins in Arabidopsis Leaf and Root Tissue Determined by Metabolic Labeling and Mass Spectrometry

被引:9
作者
Bernfur, Katja [1 ]
Larsson, Olaf [2 ]
Larsson, Christer [1 ]
Gustavsson, Niklas [3 ]
机构
[1] Lund Univ, Ctr Mol Prot Sci, Dept Biochem & Struct Biol, Lund, Sweden
[2] Huddinge Univ Hosp, Mutat Anal Facil, Clin Res Ctr, Novum, Stockholm, Sweden
[3] Novo Nordisk AS, Malov, Denmark
来源
PLOS ONE | 2013年 / 8卷 / 08期
关键词
GENE ENCODES; ARABINOGALACTAN PROTEINS; DIFFERENTIAL EXPRESSION; SNARE PROTEIN; REVEALS; FAMILY; QUANTITATION; PROTEOMICS; THALIANA; ATPASE;
D O I
10.1371/journal.pone.0071206
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Metabolic labeling of proteins with a stable isotope (N-15) in intact Arabidopsis plants was used for accurate determination by mass spectrometry of differences in protein abundance between plasma membranes isolated from leaves and roots. In total, 703 proteins were identified, of which 188 were predicted to be integral membrane proteins. Major classes were transporters, receptors, proteins involved in membrane trafficking and cell wall-related proteins. Forty-one of the integral proteins, including nine of the 13 isoforms of the PIP (plasma membrane intrinsic protein) aquaporin subfamily, could be identified by peptides unique to these proteins, which made it possible to determine their relative abundance in leaf and root tissue. In addition, peptides shared between isoforms gave information on the proportions of these isoforms. A comparison between our data for protein levels and corresponding data for mRNA levels in the widely used database Genevestigator showed an agreement for only about two thirds of the proteins. By contrast, localization data available in the literature for 21 of the 41 proteins show a much better agreement with our data, in particular data based on immunostaining of proteins and GUS-staining of promoter activity. Thus, although mRNA levels may provide a useful approximation for protein levels, detection and quantification of isoform-specific peptides by proteomics should generate the most reliable data for the proteome.
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页数:12
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