Gasilova Natalia, Girault Hubert H
Laboratoire d'Electrochimie Physique et Analytique, Ecole Polytechnique Fédérale de Lausanne , Station 6, CH-1015 Lausanne, Switzerland.
Anal Chem. 2014 Jul 1;86(13):6337-45. doi: 10.1021/ac500525n. Epub 2014 Jun 20.
Component-resolved diagnostic (CRD) of cow's milk allergy has been performed using immunoaffinity capillary electrophoresis (IACE) coupled with matrix-assisted laser desorption/ionization mass spectrometry (MALDI MS). First, total IgE quantification in the blood serum of a milk allergic patient by the IACE-UV technique was developed using magnetic beads (MBs) coated with antihuman IgE antibodies (Abs) to perform the general allergy diagnosis. Then, the immunocomplex of antihuman IgE Abs with the patient IgE Abs, obtained during the total IgE analysis, was chemically cross-linked on the MBs surface. Prepared immunosupport was used for the binding of individual milk allergens to identify the proteins triggering the allergy by IACE with UV and MALDI MS detection. Then, allergy CRD was also performed directly with milk fractions. Bovine serum albumin, lactoferrin, and α-casein (S1 and S2 forms, as was revealed by MALDI MS) were found to bind with the extracted IgE Abs, indicating that the chosen patient is allergic to these proteins. The results were confirmed by performing classical enzyme-linked immunosorbent assay of total and specific IgE Abs. The present IACE-UV/MALDI MS method required only 2 μL of blood serum and allowed the performance of the total IgE quantification and CRD of the food allergy not only with the purified allergen molecules but also directly with the food extract. Such an approach opens the possibility for direct identification of allergens molecular mass and structure, discovery of unusual allergens, which could be useful for precise personalized allergy diagnostic, allergens epitope mapping, and cross-reactivity studies.
已使用免疫亲和毛细管电泳(IACE)结合基质辅助激光解吸/电离质谱(MALDI MS)对牛奶过敏进行了组分分辨诊断(CRD)。首先,通过IACE-UV技术,利用包被抗人IgE抗体(Abs)的磁珠(MBs)对牛奶过敏患者血清中的总IgE进行定量,以进行一般过敏诊断。然后,在总IgE分析过程中获得的抗人IgE Abs与患者IgE Abs的免疫复合物在MBs表面进行化学交联。制备的免疫支持物用于结合单个牛奶过敏原,通过IACE结合UV和MALDI MS检测来鉴定引发过敏的蛋白质。然后,也直接对牛奶组分进行过敏CRD。发现牛血清白蛋白、乳铁蛋白和α-酪蛋白(MALDI MS显示为S1和S2形式)与提取出 的IgE Abs结合,表明所选患者对这些蛋白质过敏。通过对总IgE Abs和特异性IgE Abs进行经典的酶联免疫吸附测定,证实了结果。目前的IACE-UV/MALDI MS方法仅需2μL血清,不仅可以对纯化的过敏原分子进行总IgE定量和食物过敏的CRD,还可以直接对食物提取物进行。这种方法为直接鉴定过敏原的分子量和结构、发现不寻常的过敏原开辟了可能性,这对于精确的个性化过敏诊断、过敏原表位作图和交叉反应性研究可能是有用的。