Schwager Christian, Kull Skadi, Krause Susanne, Schocker Frauke, Petersen Arnd, Becker Wolf-Meinhard, Jappe Uta
Division of Clinical and Molecular Allergology, Research Center Borstel, Airway Research Center North (ARCN), Member of the German Center for Lung Research (DZL), Borstel, Germany.
Division of Clinical and Molecular Allergology, Research Center Borstel, Airway Research Center North (ARCN), Member of the German Center for Lung Research (DZL), Borstel, Germany; Department of Dermatology, Allergology and Venereology, University of Luebeck, Germany.
PLoS One. 2015 Apr 10;10(4):e0123419. doi: 10.1371/journal.pone.0123419. eCollection 2015.
Peanut allergy is one of the most severe class I food allergies with increasing prevalence. Especially lipophilic allergens, such as oleosins, were found to be associated with severe symptoms, but are usually underrepresented in diagnostic extracts. Therefore, this study focused on isolation, molecular characterization and assessment of the allergenicity of peanut oleosins.
A comprehensive method adapted for the isolation of peanut oil bodies of high purity was developed comprising a stepwise removal of seed storage proteins from oil bodies. Further separation of the oil body constituents, including the allergens Ara h 10, Ara h 11, the presumed allergen oleosin 3 and additional oleosin variants was achieved by a single run on a preparative electrophoresis cell. Protein identification realized by N-terminal sequencing, peptide mass fingerprinting and homology search revealed the presence of oleosins, steroleosins and a caleosin. Immunoblot analysis with sera of peanut-allergic individuals illustrated the IgE-binding capacity of peanut-derived oleosins.
Our method is a novel way to isolate all known immunologically distinct peanut oleosins simultaneously. Moreover, we were able to provide evidence for the allergenicity of oleosins and thus identified peanut oleosins as probable candidates for component-resolved allergy diagnosis.
花生过敏是最严重的I类食物过敏之一,其患病率呈上升趋势。尤其是亲脂性过敏原,如油质蛋白,被发现与严重症状有关,但在诊断提取物中通常含量较低。因此,本研究聚焦于花生油质蛋白的分离、分子特征分析及过敏原性评估。
开发了一种适用于分离高纯度花生油体的综合方法,包括从油体中逐步去除种子储存蛋白。通过在制备型电泳槽上单次运行,进一步分离了油体成分,包括过敏原Ara h 10、Ara h 11、推测的过敏原油质蛋白3和其他油质蛋白变体。通过N端测序、肽质量指纹图谱和同源性搜索进行的蛋白质鉴定揭示了油质蛋白、固醇油质蛋白和钙结合蛋白的存在。用花生过敏个体的血清进行免疫印迹分析表明了花生衍生油质蛋白的IgE结合能力。
我们的方法是一种同时分离所有已知免疫上不同的花生油质蛋白的新方法。此外,我们能够为油质蛋白的过敏原性提供证据,从而将花生油质蛋白鉴定为成分解析过敏诊断的可能候选物。