Abstract
Food products are subjected to adulteration, with consequent nutritional or economic loss for consumers and with damage to the commercial reputation of producers and trade labels. Substances used for adulteration range from synthetic chemicals to poor-quality plant or animal materials added to food preparations. Currently, a variety of analytical methods can be exploited to determine the presence of undeclared or unexpected ingredients in food products. Although conventional analytical tools have good potential for detecting the synthetic adulterants of food and agricultural foodstuffs, these methods often fail to identify the addition of low-quality materials to higher-value products, as in the case of typical and Protected Denomination of Origin foods. In the last years, the application of the “omic” technologies in food science has assumed a leading role in the definition of the entire and detailed (bio)chemical composition of a food and its modification along the artisanal or industrial production chain to evaluate its technological properties. These developments are driven by the need to meet the instances of food industries, regulatory agencies, and consumers in order to guarantee food quality and authenticity. Although, in principle, any class of food constituents can be a marker of the food characteristics, more than other fractions, proteins retain the record of the treatment and processes a food undergoes from raw materials to end products. This chapter focuses on the application of the newly born proteomic technologies to the discovery and characterization of reliable molecular markers of food adulteration for the assessment of food quality, typicality, and authenticity.
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Abbreviations
- 1D:
-
Mono-dimensional
- 2-D:
-
Two-dimensional
- AQUA:
-
Absolute quantification
- BLG:
-
Beta-lactoglobulin
- CE:
-
Capillary electrophoresis
- CID:
-
Collision-induced dissociation
- CML:
-
Nε-carboxymethyl-lysine
- CZE:
-
Capillary zone electrophoresis
- DIGE:
-
Differential in-gel electrophoresis
- ELISA:
-
Enzyme-linked immunosorbent assay
- ESI:
-
Electrospray ionization
- GC:
-
Gas chromatography
- GMO:
-
Genetically modified organism
- HPLC:
-
High-performance liquid chromatography
- ICAT:
-
Isotope-coded affinity tag
- IEF:
-
Isoelectric focusing
- IEX:
-
Ion exchange
- IT:
-
Ion trap
- iTRAQ:
-
Isobaric tags for relative and absolute quantitation
- LAL:
-
Lysinoalanine
- LC:
-
Liquid chromatography
- LMW:
-
Low molecular weight
- LOD:
-
Limit of detection
- LOQ:
-
Limit of quantification
- MALDI:
-
Matrix-assisted laser desorption ionization
- MM:
-
Mechanically recovered meat
- MP:
-
Milk powders
- MRM:
-
Multiple reaction monitoring
- MS/MS and MSn :
-
Tandem mass spectrometry
- MS:
-
Mass spectrometry
- MudPIT:
-
Multidimensional protein identification technology
- PAGE:
-
Polyacrylamide gel electrophoresis
- PCR:
-
Polymerase chain reaction
- PDO:
-
Protected denomination of origin: RP-HPLC: reverse-phase high-performance liquid chromatography
- SDS:
-
Sodium dodecyl-sulphate
- SILAC:
-
Stable isotope labeling with amino acids in cell culture
- SIM:
-
Single ion monitoring
- SRM:
-
Selected reaction monitoring
- TOF:
-
Time-of-flight
- UPLC-FT-ICR-MS:
-
Ultrahigh-pressure liquid chromatography high-resolution Fourier-transform ion cyclotron resonance mass spectrometry
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Mamone, G., Picariello, G., Nitride, C., Addeo, F., Ferranti, P. (2013). The Role of Proteomics in the Discovery of Marker Proteins of Food Adulteration. In: Toldrá, F., Nollet, L. (eds) Proteomics in Foods. Food Microbiology and Food Safety, vol 2. Springer, Boston, MA. https://doi.org/10.1007/978-1-4614-5626-1_24
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