Physicochemical and immunological characterization of Amb a 12, a novel ragweed (Ambrosia artemisiifolia) pollen allergen

被引:7
|
作者
Grijincu, Manuela [1 ,2 ]
Hutu, Ioan [3 ]
Weber, Milena [4 ]
Babaev, Elijahu [5 ]
Stolz, Frank [5 ]
Valenta, Rudolf [4 ,6 ,7 ,8 ]
Paunescu, Virgil
Panaitescu, Carmen [1 ,2 ,9 ]
Chen, Kuan-Wei [2 ]
机构
[1] Victor Babes Univ Med & Pharm, Ctr Immuno physiol & Biotechnol, Dept Funct Sci, Timisoara, Romania
[2] Pius Brinzeu Cty Clin Emergency Hosp, OncoGen Ctr, Timisoara, Romania
[3] Univ Life Sci King Mihai I Romania, Timisoara, Romania
[4] Med Univ Vienna, Ctr Pathophysiol, Dept Pathophysiol & Allergy Res, Div Immunopathol, Vienna, Austria
[5] Vienna Competence Ctr, Biomay AG, Vienna, Austria
[6] NRC Inst Immunol FMBA Russia, Moscow, Russia
[7] Sechenov First State Med Univ, Dept Clin Immunol & Allergy, Moscow, Russia
[8] Karl Landsteiner Univ Hlth Sci, Krems, Austria
[9] Victor Babes Univ Med & Pharm, Immuno physiol & Biotechnol Ctr, Dept Funct Sci, Sq Eftimie Murgu 2, Timisoara 300041, Romania
关键词
Ragweed; Enolase; Sensitization rate; Plant allergens; COMMON RAGWEED; CLIMATE-CHANGE; ENOLASE ALLERGEN; IDENTIFICATION; PROTEIN; L; DIAGNOSIS; LATEX; SENSITIZATION; EXPRESSION;
D O I
10.1016/j.molimm.2023.03.012
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
Background: Ragweed is an invasive plant in Europe, causing hay fever and asthma in allergic patients. Climate change is predicted to increase expansion and allergenicity. Elevated NO2 induced upregulation of a new allergen in ragweed pollen, an enolase, Amb a 12.Objective: of this study was producing ragweed enolase as a recombinant protein and characterizing its physi-cochemical and immunological features.Methods: Amb a 12 was designed for E. coli and insect cell expression. Physicochemical features were determined by mass spectrometry, circular dichroism measurements and enzymatic activity assay. Immunological charac-teristics were determined in ELISA, in a mediator release assay and by investigation of association with clinical symptoms. Common allergen sources were screened for similar proteins.Results: Ragweed enolase was produced as a 48 kDa protein forming oligomers in both expression systems, showing differences in secondary structure content and enzymatic activity depending on expression system. IgE frequency and allergenicity were low regardless of expression system. Enolase-specific serum bound to similar sized molecules in mugwort, timothy grass and birch pollen, as well as food allergen sources, while highest IgE inhibition was achieved with peach pulp extract.Conclusions: Amb a 12 had high sequence similarity and comparable IgE frequency to enolase allergens from different sources. 50 kDa proteins were found in other pollen and food allergen sources, suggesting that enolases might be pan-allergens in pollen and plant foods.
引用
收藏
页码:18 / 29
页数:12
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