Down-regulation of the strawberry Bet v 1-homologous allergen in concert with the flavonoid biosynthesis pathway in colorless strawberry mutant

被引:88
作者
Hierno, K
Alm, R
Canbäck, B
Matthiesen, R
Trajkovski, K
Björk, L
Roepstorff, P
Emanuelsson, C
机构
[1] Lund Univ, Dept Biochem, Ctr Chem & Chem Engn, S-22100 Lund, Sweden
[2] Univ So Denmark, Dept Biochem & Mol Biol, Odense, Denmark
[3] Lund Univ, Dept Microbial Ecol, S-22100 Lund, Sweden
[4] Uppsala Univ, Dept Systemat Bot, Uppsala, Sweden
关键词
allergens; de novo sequencing; differential protein expression; fluorescent two-dimensional differential gel electrophoresis protein identification;
D O I
10.1002/pmic.200500469
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Proteomic screening of strawberry (Fragaria ananassa) yielded a 58% success rate in protein identification in spite of the fact that no genomic sequence is available for this species. This was achieved by a combination of MALDI-MS/MS de novo sequencing of double-derivatized peptides and indel-tolerant searching against local protein databases built on both EST and full-length nucleotide sequences. The amino acid sequence of a strawberry allergen, homologous to the well-known major birch pollen allergen Bet v 1, was partially determined. This strawberry allergen, named Fra a 1 according to the nomenclature for allergen proteins, showed sequence identity of 54 and 77%, respectively, with corresponding allergens from birch and apple. Differential expression, as evaluated by 2-D DIGE, occurred in 10% of protein spots when red strawberries were compared to a colorless (white) strawberry mutant. White strawberries, known to be tolerated by individuals affected by allergy, were found to be virtually free from the strawberry allergen. Also several enzymes in the pathway for biosynthesis of flavonoids, to which the red color pelargonidin belongs, were down-regulated. This approach to assess differential protein expression without access to genomic sequence information can also be applied to other crop plants and phenotypic traits.
引用
收藏
页码:1574 / 1587
页数:14
相关论文
共 47 条
[21]   The EMBL nucleotide sequence database [J].
Kulikova, T ;
Aldebert, P ;
Althorpe, N ;
Baker, W ;
Bates, K ;
Browne, P ;
van den Broek, A ;
Cochrane, G ;
Duggan, K ;
Eberhardt, R ;
Faruque, N ;
Garcia-Pastor, M ;
Harte, N ;
Kanz, C ;
Leinonen, R ;
Lin, Q ;
Lombard, V ;
Lopez, R ;
Mancuso, R ;
McHale, M ;
Nardone, F ;
Silventoinen, V ;
Stoehr, P ;
Stoesser, G ;
Tuli, MA ;
Tzouvara, K ;
Vaughan, R ;
Wu, D ;
Zhu, WM ;
Apweiler, R .
NUCLEIC ACIDS RESEARCH, 2004, 32 :D27-D30
[22]   Improved Ruthenium II tris (bathophenantroline disulfonate) staining and destaining protocol for a better signal-to-background ratio and improved baseline resolution [J].
Lamanda, A ;
Zahn, A ;
Röder, D ;
Langen, H .
PROTEOMICS, 2004, 4 (03) :599-608
[23]  
Larsen MR, 2002, PROTEOMICS, V2, P1277, DOI 10.1002/1615-9861(200209)2:9<1277::AID-PROT1277>3.0.CO
[24]  
2-P
[25]   Mass spectrometric identification of proteins and characterization of their post-translational modifications in proteome analysis [J].
Larsen, MR ;
Roepstorff, P .
FRESENIUS JOURNAL OF ANALYTICAL CHEMISTRY, 2000, 366 (6-7) :677-690
[26]   Combination of two matrices results in improved performance of MALDI MS for peptide mass mapping and protein analysis [J].
Laugesen, S ;
Roepstorff, P .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 2003, 14 (09) :992-1002
[27]   Automated methods for improved protein identification by peptide mass fingerprinting [J].
Levander, F ;
Rögnvaldsson, T ;
Samuelsson, J ;
James, P .
PROTEOMICS, 2004, 4 (09) :2594-2601
[28]   Proteomic analysis of post-translational modifications [J].
Mann, M ;
Jensen, ON .
NATURE BIOTECHNOLOGY, 2003, 21 (03) :255-261
[29]   Charge derivatization by 4-sulfophenyl isothiocyanate enhances peptide sequencing by post-source decay matrix-assisted laser desorption/ionization time-of-flight mass spectrometry [J].
Marekov, LN ;
Steinert, PM .
JOURNAL OF MASS SPECTROMETRY, 2003, 38 (04) :373-377
[30]   Interpreting peptide mass spectra by VEMS [J].
Matthiesen, R ;
Lundsgaard, M ;
Welinder, KG ;
Bauw, G .
BIOINFORMATICS, 2003, 19 (06) :792-793