Zailatul H M Y, Rosmilah M, Faizal B, Noormalin A, Shahnaz M
Allergy and Immunology Research Centre, Institute for Medical Research, Jalan Pahang, 50588 Kuala Lumpur, Malaysia.
Department of Biology, Faculty of Science and Mathematics, Universiti Pendidikan Sultan Idris, 35900 Tanjong Malim, Perak, Malaysia.
Trop Biomed. 2015 Jun;32(2):323-34.
The purpose of this study was to evaluate the effect of different cooking methods on the allergenicity of cockle and to identify proteins most frequently bound by IgE antibodies using a proteomics approach. Raw, boiled, fried and roasted extracts of the cockle were prepared. The protein profiles of the extracts were obtained by separation using sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) and 2-dimensional gel electrophoresis (2-DE). IgE-immunoblotting was then performed with the use of individual sera from patients with cockle allergy and the major IgE-binding proteins were analyzed by mass-spectrometry. SDS-PAGE of raw extract showed 13 protein bands. Smaller numbers of protein bands were detected in the boiled, fried and roasted extracts. The 2-DE gel profile of the raw extract further separated the protein bands to ~50 protein spots with molecular masses between 13 to 180 kDa and isoelectric point (pI) values ranging from 3 to 10. Immunoblotting of raw extract exhibited 11 IgE-binding proteins with two proteins of 36 and 40 kDa as the major IgE-binding proteins, while the boiled extract revealed 3 IgE-binding proteins. Fried and roasted extracts only showed a single IgE-binding protein at 36 kDa. 2-DE immunoblotting of raw extract demonstrated 5 to 20 IgE reactive spots. Mass spectrometry analysis led to identification of 2 important allergens, tropomyosin (36 kDa) and arginine kinase (40 kDa). Heated extracts showed a reduction in the number of IgE-reactive bands compared with raw extract, which suggest that thermal treatment can be used as a tool in attempting to reduce cockle allergenicity. The degree of allergenicity of cockle was demonstrated in the order raw > boiled > fried ≈ roasted. Two important allergens reacting with more than 50% of patients' sera identified using mass spectrometric approaches were tropomyosin and arginine kinase. Thus, allergens found in this study would help in component based diagnosis, management of cockle allergic patients and to the standardisation of allergenic test products as tools in molecular allergology.
本研究的目的是评估不同烹饪方法对鸟蛤变应原性的影响,并使用蛋白质组学方法鉴定最常与IgE抗体结合的蛋白质。制备了鸟蛤的生、煮、煎和烤提取物。通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)和二维凝胶电泳(2-DE)分离获得提取物的蛋白质谱。然后使用鸟蛤过敏患者的个体血清进行IgE免疫印迹,并通过质谱分析主要的IgE结合蛋白。生提取物的SDS-PAGE显示13条蛋白带。在煮、煎和烤提取物中检测到的蛋白带数量较少。生提取物的2-DE凝胶图谱进一步将蛋白带分离为约50个蛋白点,分子量在13至180 kDa之间,等电点(pI)值范围为3至10。生提取物的免疫印迹显示11种IgE结合蛋白,其中36 kDa和40 kDa的两种蛋白为主要的IgE结合蛋白,而煮提取物显示3种IgE结合蛋白。煎和烤提取物仅在36 kDa处显示单一的IgE结合蛋白。生提取物的2-DE免疫印迹显示5至20个IgE反应性斑点。质谱分析鉴定出2种重要的变应原,原肌球蛋白(36 kDa)和精氨酸激酶(40 kDa)。与生提取物相比,加热提取物显示IgE反应性条带数量减少,这表明热处理可作为降低鸟蛤变应原性的一种手段。鸟蛤的变应原性程度依次为生>煮>煎≈烤。使用质谱方法鉴定出与超过50%患者血清反应的两种重要变应原是原肌球蛋白和精氨酸激酶。因此,本研究中发现的变应原将有助于基于成分的诊断、鸟蛤过敏患者的管理以及变应原测试产品的标准化,作为分子变应学中的工具。