Ruiz Orduna Alberto, Husby Erik, Yang Charles T, Ghosh Dipankar, Beaudry Francis
a Département de biomédecine vétérinaire, Faculté de médecine vétérinaire , Université de Montréal , Saint-Hyacinthe , QC , Canada.
b Department of Environment & Food Safety , Thermo Fisher Scientific , San Jose , CA , USA.
Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 2015;32(10):1709-17. doi: 10.1080/19440049.2015.1064173. Epub 2015 Aug 4.
In recent years a significant increase of food fraud has been observed, ranging from false label claims to the use of additives and fillers to increase profitability. Recently in 2013 horse and pig DNAs were detected in beef products sold from several retailers. Mass spectrometry (MS) has become the workhorse in protein research, and the detection of marker proteins could serve for both animal species and tissue authentication. Meat species authenticity is performed in this paper using a well-defined proteogenomic annotation, carefully chosen surrogate tryptic peptides and analysis using a hybrid quadrupole-Orbitrap MS. Selected mammalian meat samples were homogenised and proteins were extracted and digested with trypsin. The samples were analysed using a high-resolution MS. Chromatography was achieved using a 30-min linear gradient along with a BioBasic C8 100 × 1 mm column at a flow rate of 75 µl min(-1). The MS was operated in full-scan high resolution and accurate mass. MS/MS spectra were collected for selected proteotypic peptides. Muscular proteins were methodically analysed in silico in order to generate tryptic peptide mass lists and theoretical MS/MS spectra. Following a comprehensive bottom-up proteomic analysis, we detected and identified a proteotypic myoglobin tryptic peptide (120-134) for each species with observed m/z below 1.3 ppm compared with theoretical values. Moreover, proteotypic peptides from myosin-1, myosin-2 and β-haemoglobin were also identified. This targeted method allowed comprehensive meat speciation down to 1% (w/w) of undesired product.
近年来,食品欺诈现象显著增加,从虚假标签声明到使用添加剂和填充物以提高利润率等不一而足。2013年,近期在几家零售商出售的牛肉产品中检测到马和猪的DNA。质谱(MS)已成为蛋白质研究的主力军,标记蛋白的检测可用于动物物种和组织鉴定。本文采用明确的蛋白质基因组注释、精心挑选的替代胰蛋白酶肽段,并使用四极杆-轨道阱联用质谱进行分析,以鉴定肉类物种的真实性。选取的哺乳动物肉类样本经匀浆处理,提取蛋白质并用胰蛋白酶消化。样本采用高分辨率质谱进行分析。使用30分钟线性梯度洗脱,搭配BioBasic C8 100×1 mm色谱柱,流速为75 μl min⁻¹实现色谱分离。质谱仪在全扫描高分辨率和精确质量模式下运行。对选定的蛋白型肽段采集二级质谱(MS/MS)谱图。对肌肉蛋白进行系统的计算机分析,以生成胰蛋白酶肽段质量列表和理论二级质谱谱图。经过全面的自下而上蛋白质组学分析,我们检测并鉴定出每个物种的一种蛋白型肌红蛋白胰蛋白酶肽段(120 - 134),其观测质荷比与理论值相比偏差低于1.3 ppm。此外,还鉴定出了来自肌球蛋白-1、肌球蛋白-2和β-血红蛋白的蛋白型肽段。这种靶向方法能够实现对低至1%(w/w)的非目标产品进行全面的肉类物种鉴定。