Manfredi Anita, Mattarozzi Monica, Giannetto Marco, Careri Maria
Dipartimento di Chimica, Università degli Studi di Parma, Parco Area delle Scienze 17/A, 43124, Parma, Italy.
Dipartimento di Chimica, Università degli Studi di Parma, Parco Area delle Scienze 17/A, 43124, Parma, Italy.
Anal Chim Acta. 2015 Oct 1;895:62-70. doi: 10.1016/j.aca.2015.09.008. Epub 2015 Sep 12.
Celiac patients should feel confident in the safety of foods labelled or expected to be gluten-free. In this context, a targeted proteomic approach based on liquid chromatography-electrospray ionization-tandem mass spectrometry (LC-ESI-MS/MS) technique was proposed to assess the presence of celiotoxic cereals, namely wheat, oats, barley and rye, in raw and processed food products. To this aim, unique marker peptides were properly selected in order to distinguish between the different cereal types. A revised cocktail solution based on reducing and denaturing agents was exploited for prolamin extraction from raw and processed food; in addition, defatting with hexane was carried out for sample clean-up, allowing to largely reduce problems related to matrix effect. Method validation on fortified rice flour showed good analytical performance in terms of sensitivity (limits of detection in the 2-18 mg kg(-1) range). However, poor trueness was calculated for self-made incurred bread (between 3 and 30% depending on the peptide), probably due to baking processes, which reduce gluten extractability. Thus, it is evident that in the case of processed foods further insights into sample treatment efficiency and reference materials for protein calibration are required to obtain accurate gluten determination. Finally, the developed method was applied for the analysis of market food products, offering the possibility to discriminate among cereals, with good agreement with labelled ingredients for gluten-containing foodstuffs.
乳糜泻患者应对标记为或预期为无麸质的食品安全性充满信心。在此背景下,提出了一种基于液相色谱 - 电喷雾电离 - 串联质谱(LC - ESI - MS/MS)技术的靶向蛋白质组学方法,以评估生食品和加工食品中细胞毒性谷物(即小麦、燕麦、大麦和黑麦)的存在情况。为此,适当选择了独特的标记肽,以区分不同的谷物类型。利用一种基于还原剂和变性剂的改良混合溶液从生食品和加工食品中提取醇溶蛋白;此外,用己烷脱脂进行样品净化,从而在很大程度上减少与基质效应相关的问题。在强化米粉上进行的方法验证在灵敏度方面表现出良好的分析性能(检测限在2 - 18 mg kg⁻¹范围内)。然而,对于自制的含麸质面包,计算得出的准确性较差(取决于肽,在3%至30%之间),这可能是由于烘焙过程降低了麸质的可提取性。因此,很明显,对于加工食品,需要进一步深入了解样品处理效率和用于蛋白质校准的参考材料,以获得准确的麸质测定结果。最后,所开发的方法应用于市售食品的分析,能够区分谷物,与含麸质食品的标记成分具有良好的一致性。