Magnetic particles functionalized with PAMAM-dendrimers and antibodies: a new system for an ELISA method able to detect Ara h3/4 peanut allergen in foods

An innovative enzyme-linked immunosorbent assay (ELISA) format based on antibody-coated magnetic micro-particles (MPs) for the sensitive detection of Ara h3/4 allergen in food is described. The immunosupport is suspended in the incubation solutions and the MPs with the captured allergen can be easily harvested on a magnet, separated from the solutions, and washed using an easy-to-use, fast and selective approach that allows its detection and quantification. Two differently coated MPs, ProteinA-Pn-b and MP-NH2-PAMAM G 1.5 -Pn-b immunosupports, were tested. The functionalization of the MPs with PAMAM-sodium carboxylate dendrimers elicits a major stability on the immunoglobulin activity resulting in a threefold enhancement of the analytical sensitivity for the assay with respect to a ProteinA immobilization. Validation was carried out on two different matrices: corn flakes and biscuits. In the case of MP-NH2-PAMAM G 1.5 -Pn-b immunosupport, limit of detection was found to be 0.2 mg peanuts/kg matrix in both matrices; the linear response range was demonstrated from 2.5 to 15 mg peanuts/kg matrix by performing statistical tests (homoscedasticity and Mandel fitting tests). Good accuracy and recovery (>80 ± 2%) were obtained. Different food samples were tested and the results were compared with those obtained with a commercially available ELISA kit. The results obtained in this work demonstrated the applicability of the immunomagnetic ELISA methods on real samples and the possibility to perform the assay with significantly reduced reagent and sample consumption.

[1]  Guoqing Shen,et al.  A class-specific enzyme-linked immunosorbent assay based on magnetic particles for multiresidue organophosphorus pesticides. , 2010, Journal of agricultural and food chemistry.

[2]  Jin-Ming Lin,et al.  Development of a rapid and sensitive magnetic chemiluminescent enzyme immunoassay for detection of luteinizing hormone in human serum. , 2009, Clinical biochemistry.

[3]  C. Bala,et al.  Sensitive Aflatoxin B1 Determination Using a Magnetic Particles-Based Enzyme-Linked Immunosorbent Assay , 2008, Sensors.

[4]  James R. McElhanon,et al.  Dendrimer-activated surfaces for high density and high activity protein chip applications. , 2004, Langmuir : the ACS journal of surfaces and colloids.

[5]  P. Singh Terminal groups in Starburst dendrimers: activation and reactions with proteins. , 1998, Bioconjugate chemistry.

[6]  William A. Goddard,et al.  Starburst Dendrimers: Molecular‐Level Control of Size, Shape, Surface Chemistry, Topology, and Flexibility from Atoms to Macroscopic Matter , 1990 .

[7]  Donald A Tomalia,et al.  Dendrimers in biomedical applications--reflections on the field. , 2005, Advanced drug delivery reviews.

[8]  Gregory Stephanopoulos,et al.  Carboxyl-terminated dendrimer-coated bioactive interface for protein microarray: high-sensitivity detection of antigen in complex biological samples. , 2007, Langmuir : the ACS journal of surfaces and colloids.

[9]  J. Marty,et al.  Biomolecule immobilization in biosensor development: tailored strategies based on affinity interactions. , 2008, Protein and peptide letters.

[10]  Francis C Szoka,et al.  Designing dendrimers for biological applications , 2005, Nature Biotechnology.

[11]  S. Vieths,et al.  Development of a real-time PCR and a sandwich ELISA for detection of potentially allergenic trace amounts of peanut (Arachis hypogaea) in processed foods. , 2004, Journal of agricultural and food chemistry.

[12]  L. Elviri,et al.  Use of specific peptide biomarkers for quantitative confirmation of hidden allergenic peanut proteins Ara h 2 and Ara h 3/4 for food control by liquid chromatography–tandem mass spectrometry , 2007, Analytical and bioanalytical chemistry.

[13]  U. Haberkorn,et al.  Antibody-dendrimer conjugates: the number, not the size of the dendrimers, determines the immunoreactivity. , 2008, Bioconjugate chemistry.

[14]  L. Elviri,et al.  ICP-MS as a novel detection system for quantitative element-tagged immunoassay of hidden peanut allergens in foods , 2007, Analytical and bioanalytical chemistry.

[15]  Philip R Goodwin,et al.  Food allergen detection methods: a coordinated approach. , 2004, Journal of AOAC International.

[16]  S. Vieths,et al.  Detection of potentially allergenic hazelnut (Corylus avellana) residues in food: a comparative study with DNA PCR-ELISA and protein sandwich-ELISA. , 2002, Journal of agricultural and food chemistry.

[17]  Maria Careri,et al.  Selective and rapid immunomagnetic bead-based sample treatment for the liquid chromatography-electrospray ion-trap mass spectrometry detection of Ara h3/4 peanut protein in foods. , 2008, Journal of chromatography. A.