Analysis of egg-based model wall paintings by use of an innovative combined dot-ELISA and UPLC-based approach

• Published in: Analytical and bioanalytical chemistry 2013-01, Vol.405 (2-3), p.691-701
• Main Authors: Potenza, Mariangela, Sabatino, Giuseppina, Giambi, Francesca, Rosi, Luca, Papini, Anna Maria, Dei, Luigi
• Format: Article
• Language: English
• Subjects: Amino acids; Amino Acids - analysis; Analytical Chemistry; Antigens; Binders; Biochemistry; Characterization and Evaluation of Materials; Chemical analysis; Chemical properties; Chemistry; Chemistry and Materials Science; Chromatography; Chromatography, High Pressure Liquid - methods; Composition; Cultural heritage; Egg (Biology); Egg Proteins - chemistry; Eggs - analysis; Enzyme-linked immunosorbent assay; Enzyme-Linked Immunosorbent Assay - methods; Enzymes; Food Science; High performance liquid chromatography; Identification and classification; Immunology; Laboratory Medicine; Liquid chromatography; Mathematical analysis; Methods; Microscopy; Monitoring/Environmental Analysis; Original Paper; Paint - analysis; Proteins; Reflectance; Staining; Walls
• ISSN: 1618-2642; 1618-2650
• DOI: 10.1007/s00216-012-6049-9

The chemical analysis of egg-based wall paintings—the mezzo fresco technique—is an interesting topic in the characterisation of organic binders. A revised procedure for a dot-enzyme-linked immunosorbent assay (dot-ELISA) able to detect protein components of egg-based wall paintings is reported. In the new dot-ELISA procedure we succeeded in maximizing the staining colour by adjusting the temperature during the staining reaction. Quantification of the colour intensity by visible reflectance spectroscopy resulted in a straight line plot of protein concentration against reflectance in the wavelength range 380–780 nm. The modified dot-ELISA procedure is proposed as a semi-quantitative analytical method for characterisation of protein binders in egg-based paintings. To evaluate its performance, the method was first applied to standard samples (ovalbumin, whole egg, egg white), then to model specimens, and finally to real samples (Giotto’s wall paintings). Moreover, amino acid analysis performed by innovative ultra-performance liquid chromatography was applied both to standards and to model samples and the results were compared with those from the dot-ELISA tests. In particular, after protein hydrolysis (24 h, 114 °C, 6 mol L −1 HCl) of the samples, amino acid derivatization by use of 6-aminoquinolyl- N -hydroxysuccinimidyl carbamate enabled reproducible analysis of amino acids. This UPLC amino acid analysis was rapid and reproducible and was applied for the first time to egg-based paintings. Because the painting technique involved the use of egg-based tempera on fresh lime-based mortar, the study enabled investigation of the effect of the alkaline environment on egg-protein detection by both methods. Figure Model wall paintings specimens and typical dot-ELISA stains for egg proteins.