The dominant 55 kDa allergen of the subtropical Bahia grass (Paspalum notatum) pollen is a group 13 pollen allergen, Pas n 13

被引:11
作者
Davies, Janet M. [1 ,2 ,3 ,4 ]
Voskamp, Astrid [2 ,3 ,4 ]
Dang, Thanh D. [2 ,3 ,4 ]
Pettit, Benjamin [2 ,4 ]
Loo, Dorothy [5 ]
Petersen, Arnd [6 ]
Hill, Michelle M. [5 ]
Upham, John W. [1 ]
Rolland, Jennifer M. [2 ,4 ]
O'Hehir, Robyn E. [2 ,3 ,4 ]
机构
[1] Univ Queensland, Lung & Allergy Res Ctr, Brisbane, Qld 4102, Australia
[2] Cooperat Res Ctr Asthma & Airways, Sydney, NSW 2037, Australia
[3] Alfred Hosp, Dept Allergy Immunol & Resp Med, Melbourne, Vic 3004, Australia
[4] Monash Univ, Dept Immunol, Melbourne, Vic 3004, Australia
[5] Univ Queensland, Univ Queensland Diamantina Inst, Brisbane, Qld 4102, Australia
[6] Res Ctr Borstel, D-23845 Borstel, Germany
基金
澳大利亚国家健康与医学研究理事会; 英国医学研究理事会;
关键词
Grass pollen allergens; Group 13 pollen allergen; Polygalacturonase; Bahia grass pollen; Pas n 13; IgE; PHL P 4; CROSS-REACTIVITY; IMMUNOLOGICAL CHARACTERIZATION; MOLECULAR-CLONING; EXPRESSION; IMMUNOTHERAPY; IGE; PRATENSE; PROTEIN; ASTHMA;
D O I
10.1016/j.molimm.2010.12.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Bahia grass, Paspalum notatum, is an important pollen allergen source with a long season of pollination and wide distribution in subtropical and temperate regions. We aimed to characterize the 55 kDa allergen of Bahia grass pollen (BaGP) and ascertain its clinical importance. BaGP extract was separated by 2D-PAGE and immunoblotted with serum IgE of a grass pollen-allergic patient. The amino-terminal protein sequence of the predominant allergen isoform at 55 kDa had similarity with the group 13 allergens of Timothy grass and maize pollen, Phl p 13 and Zea m 13. Four sequences obtained by rapid amplification of the allergen cDNA ends represented multiple isoforms of Pas n 13. The predicted full length cDNA for Pas n 13 encoded a 423 amino acid glycoprotein including a signal peptide of 28 residues and with a predicted pI of 7.0. Tandem mass spectrometry of tryptic peptides of 2D gel spots identified peptides specific to the deduced amino acid sequence for each of the four Pas n 13 cDNA, representing 47% of the predicted mature protein sequence of Pas n 13. There was 80.6% and 72.6% amino acid identity with Zea m 13 and Phl p 13, respectively. Reactivity with a Phl p 13-specific monoclonal antibody AF6 supported designation of this allergen as Pas n 13. The allergen was purified from BaGP extract by ammonium sulphate precipitation, hydrophobic interaction and size exclusion chromatography. Purified Pas n 13 reacted with serum IgE of 34 of 71(48%) grass pollen-allergic patients and specifically inhibited IgE reactivity with the 55 kDa band of BaGP for two grass pollen-allergic donors. Four isoforms of Pas n 13 from pl 6.3-7.8 had IgE-reactivity with grass pollen allergic sera. The allergenic activity of purified Pas n 13 was demonstrated by activation of basophils from whole blood of three grass pollen-allergic donors tested but not control donors. Pas n 13 is thus a clinically relevant pollen allergen of the subtropical Bahia grass likely to be important in eliciting seasonal allergic rhinitis and asthma in grass pollen-allergic patients. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:931 / 940
页数:10
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