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采用新型夹心酶联免疫吸附测定法测定食品中低水平麸质的创新方法。

Innovative approach to low-level gluten determination in foods using a novel sandwich enzyme-linked immunosorbent assay protocol.

作者信息

Valdés Israel, García Enrique, Llorente Mercedes, Méndez Enrique

机构信息

Unidad de Gluten, Centro Nacional de Biotecnología, Madrid, Spain.

出版信息

Eur J Gastroenterol Hepatol. 2003 May;15(5):465-74. doi: 10.1097/01.meg.0000059119.41030.df.

Abstract

OBJECTIVES

There is currently much call for a reliable enzyme-linked immunosorbent assay (ELISA) protocol for determining gluten in foods to serve as a basis for further Codex Alimentarius regulations. Given its ability to recognize the potential coeliac-toxic epitope QQPFP, which occurs repeatedly in alpha-, gamma- and omega-gliadins, hordeins and secalins, the monoclonal antibody R5 raised against a secalin extract may prove to be an essential tool for gluten analysis. This study was designed to develop a highly sensitive and specific sandwich ELISA to quantify low levels of wheat, barley and rye prolamins in foods for coeliacs.

METHODS

Simple sandwich ELISA based on the use of a single monoclonal antibody (R5) as both the coating and detection was developed. A quantitative cocktail gluten-extraction procedure for heat-processed foods was also tested.

RESULTS

R5-ELISA was able to identify gliadins, hordeins and secalins with assay sensitivities of 0.78, 0.39 and 0.39 ng/ml, respectively. The assay's detection limit was 1.5 ng gliadins/ml (1.56 ppm gliadins, 3.2 ppm gluten). The system proved insensitive to the non-coeliac-toxic cereals maize, rice and oats, and was non-cultivar-dependent. It was also able to detect gliadins and hordeins in unprocessed and heat-processed wheat- and barley-based products, and to estimate the gluten content of hydrolysed foods.

CONCLUSION

We present a new generation of a robust sandwich R5-ELISA with good reproducibility (8.7%) and repeatability (7.7%). Its gluten-detection limit of 3.2 ppm is lower than the existing threshold of 20-200 ppm. The ELISA, which is equally sensitive to barley, wheat and rye prolamins, is compatible with the quantitative cocktail extraction procedure for heat-processed foods. Along with the cocktail procedure, the Working Group on Prolamin Analysis and Toxicity is currently evaluating an R5-ELISA system as proposed by the Codex Alimentarius Commission.

摘要

目的

目前,人们迫切需要一种可靠的酶联免疫吸附测定(ELISA)方案来测定食品中的麸质,以此作为食品法典委员会进一步制定法规的依据。抗黑麦醇溶蛋白提取物产生的单克隆抗体R5能够识别潜在的乳糜泻毒性表位QQPFP,该表位在α-、γ-和ω-醇溶蛋白、大麦醇溶蛋白和黑麦醇溶蛋白中反复出现,可能是麸质分析的重要工具。本研究旨在开发一种高度灵敏且特异的夹心ELISA,用于定量检测乳糜泻患者食品中低水平的小麦、大麦和黑麦醇溶蛋白。

方法

开发了一种基于使用单一单克隆抗体(R5)作为包被抗体和检测抗体的简单夹心ELISA。还测试了一种针对热处理食品的定量混合麸质提取程序。

结果

R5-ELISA能够分别以0.78、0.39和0.39 ng/ml的检测灵敏度识别醇溶蛋白、大麦醇溶蛋白和黑麦醇溶蛋白。该检测方法的检测限为1.5 ng醇溶蛋白/ml(1.56 ppm醇溶蛋白,3.2 ppm麸质)。该系统对非乳糜泻毒性谷物玉米、大米和燕麦不敏感,且不依赖品种。它还能够检测未加工和热处理的小麦和大麦制品中的醇溶蛋白和大麦醇溶蛋白,并估计水解食品中的麸质含量。

结论

我们展示了新一代稳健的夹心R5-ELISA,具有良好的重现性(8.7%)和重复性(7.7%)。其3.2 ppm的麸质检测限低于现有的20 - 200 ppm阈值。该ELISA对大麦、小麦和黑麦醇溶蛋白同样敏感,与热处理食品的定量混合提取程序兼容。连同混合提取程序,醇溶蛋白分析与毒性工作组目前正在评估食品法典委员会提议的R5-ELISA系统。

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