Affiliations 

  • 1 Halal Products Research Institute, Universiti Putra Malaysia, Selangor, Malaysia
  • 2 Halal Products Research Institute, Universiti Putra Malaysia, Selangor, Malaysia; Department of Nutrition and Dietetic, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Selangor, Malaysia
  • 3 Institute of Biological Sciences, University of Malaya, Kuala Lumpur, Malaysia; University of Malaya Center for Proteomics Research, University of Malaya, Kuala Lumpur, Malaysia
  • 4 Halal Products Research Institute, Universiti Putra Malaysia, Selangor, Malaysia; Department of Animal Science, Faculty of Agriculture, Universiti Putra Malaysia, Selangor, Malaysia. Electronic address: awis@upm.edu.my
Food Chem, 2016 May 15;199:157-64.
PMID: 26775957 DOI: 10.1016/j.foodchem.2015.11.121

Abstract

The purpose of this study was to identify porcine-specific peptide markers from thermally processed meat that could differentiate pork from beef, chevon and chicken meat. In the initial stage, markers from tryptic digested protein of chilled, boiled and autoclaved pork were identified using LC-QTOF-MS. An MRM method was then established for verification. A thorough investigation of LC-QTOF-MS data showed that only seven porcine-specific peptides were consistently detected. Among these peptides, two were derived from lactate dehydrogenase, one from creatine kinase, and four from serum albumin protein. However, MRM could only detect four peptides (EVTEFAK, LVVITAGAR, FVIER and TVLGNFAAFVQK) that were consistently present in pork samples. In conclusion, meat species determination through a tandem mass spectrometry platform shows high potential in providing scientifically valid and reliable results even at peptide level. Besides, the specificity and selectivity offered by the proteomics approach also provide a robust platform for Halal authentication.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.