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Isolation of recombinant antibody fragments (scFv) by phage display technology for detection of almond allergens in food products

机译:通过噬菌体展示技术分离重组抗体片段(scFv)以检测食品中的杏仁过敏原

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摘要

Tree nut allergies are considered an important health issue in developed countries. To comply with the regulations on food labeling, reliable allergen detection methods are required. In this work we isolated almond-specific recombinant antibody fragments (scFv) from a commercial phage display library bypassing the use of live animals, hence being consistent with the latest policies on animal welfare. To this end an iterative selection procedure employing the Tomlinson I phage display library and a crude almond protein extract was carried out. Two different almond-specific scFv (named PD1F6 and PD2C9) were isolated after two rounds of biopanning, and an indirect phage ELISA was implemented to detect the presence of almond protein in foodstuffs. The isolated scFvs demonstrated to be highly specific and allowed detection of 40 ng mL(-1) and 100 ng mL(-1) of raw and roasted almond protein, respectively. The practical detection limit of the assay in almond spiked food products was 0.1 mg g(-1) (110-120 ppm). The developed indirect phage ELISA was validated by analysis of 92 commercial food products, showing good correlation with the results obtained by a previously developed real-time PCR method for the detection of almond in foodstuffs. The selected phage clones can be affinity maturated to improve their sensitivity and genetically engineered to be employed in different assay formats. (C) 2015 Elsevier Ltd. All rights reserved.
机译:坚果过敏症在发达国家被认为是重要的健康问题。为了符合食品标签规定,需要可靠的过敏原检测方法。在这项工作中,我们从商业噬菌体展示库中分离了杏仁特异性重组抗体片段(scFv),从而绕过了使用活体动物的行为,因此与动物福利的最新政策保持一致。为此目的,使用Tomlinson I噬菌体展示文库和粗杏仁蛋白提取物进行了迭代选择程序。经过两轮生物淘洗后,分离出两个不同的杏仁特异性scFv(分别称为PD1F6和PD2C9),并实施了间接噬菌体ELISA来检测食品中杏仁蛋白的存在。分离的scFvs具有很高的特异性,可以分别检测40 ng mL(-1)和100 ng mL(-1)的原始和烤杏仁蛋白。杏仁加标食品中该方法的实际检测极限为0.1 mg g(-1)(110-120 ppm)。通过分析92种商业食品验证了开发的间接噬菌体ELISA,与通过先前开发的用于检测食品中杏仁的实时PCR方法获得的结果显示出良好的相关性。可以将所选噬菌体克隆亲和力成熟以提高其敏感性,并进行基因工程改造以用于不同的测定形式。 (C)2015 Elsevier Ltd.保留所有权利。

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