| Literature DB >> 27341426 |
Alessandra Altomare1, Luca Regazzoni1, Ximena Maria Paredes Parra1, Francesca Selmin1, Cristiano Rumio2, Marina Carini1, Giancarlo Aldini3.
Abstract
A validated analytical procedure is here described for the quality control of the protein fraction of purified bovine colostrum used in food supplements. The proposed procedure starts with 1D and 2D-gel electrophoresis. The sample is then separated into two fractions by protein G affinity chromatography: the IgG enriched and the IgG depleted fraction (IgG-d). A size exclusion chromatography coupled to UV is then applied to the IgG and IgG-d fractions for the quantitative analysis of IgG and IgM, respectively. The IgG-d fraction is then analysed by HPLC-MS analysis for the quantitative analysis of β-lactoglobulins and α-lactoalbumin. The next step is to quantitatively measure a set of bioactive proteins selected from the bovine colostrum data bank on the basis of their claimed health benefits. The enzymatic activities of lactoperoxidase and xanthine dehydrogenase/oxidase are then tested as an index of protein functionality.Entities:
Keywords: Bovine colostrum; Food supplement; Mass spectrometry; Quality control; Size exclusion chromatography
Mesh:
Substances:
Year: 2016 PMID: 27341426 DOI: 10.1016/j.jchromb.2016.06.013
Source DB: PubMed Journal: J Chromatogr B Analyt Technol Biomed Life Sci ISSN: 1570-0232 Impact factor: 3.205