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首页> 外文期刊>Food research international >Comparative quantification and differentiation of bracatinga (Mimosa scabrella Bentham) honeydew honey proteins using targeted peptide markers identified by high-resolution mass spectrometry
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Comparative quantification and differentiation of bracatinga (Mimosa scabrella Bentham) honeydew honey proteins using targeted peptide markers identified by high-resolution mass spectrometry

机译:使用高分辨率质谱法鉴定的靶向肽标记的靶向肽标志物的靶向肽标志物的比较定量和分化

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Honey traceability is an important topic, especially for honeydew honeys, due to the increased incidence of adulteration. This study aimed to establish specific markers to quantify proteins in honey. A proteomics strategy to identify marker peptides from bracatinga honeydew honey was therefore developed. The proteomics approach was based on initial untargeted identification of honey proteins and peptides by LC-ESI-Triple-TOF-MS/MS, which identified the major royal jelly proteins (MRJP) presence. Afterwards, the peptides were selected by the in silico digestion. The marker peptides were quantified by the developed targeted LC-QqQ-MS/MS method, which provided good linearity and specificity, besides recoveries between 92 and 100% to quantify peptides from bracatinga honeydew honey. The uniqueness and high response in mass spectrometry were backed by further complementary protein analysis (SDS-PAGE). The selected marker peptides EALPHVPIFDR (MRJP 1), ILGANVK (MRJP 2), TFVTIER (MRJP 3), QNIDVVAR (MRJP 4), FINNDYNFNEVNFR (MRJP 5) and LLQPYPDWSWTK (MRJP 7), quantified by LC-QqQ-MS/MS, highlighted that the content of QNIDVVAR from MRJP 4 could be used to differentiate bracatinga honeydew honey from floral honeys (p 0.05) as a potential marker for its authentication. Finally, principal components analysis highlighted the QNIDVVAR content as a good descriptor of the analyzed bracatinga honeydew honey samples.
机译:蜂蜜可追溯性是一个重要的话题,特别是对于蜜露蜂蜜,由于掺假发病率增加。本研究旨在建立特定标志物,以量化蜂蜜中的蛋白质。因此,开发了一种蛋白质组学策略来鉴定蜜露蜂蜜蜂蜜的标记肽。蛋白质组学方法基于LC-ESI-Triple-Tof-MS / MS的初始未确定鉴定蜂蜜蛋白和肽,其鉴定了主要蜂王浆蛋白(MRJP)存在。然后,通过硅消化选择肽。通过研制的靶向LC-QQQ-MS / MS方法量化标记肽,其提供良好的线性和特异性,除了92-100%之间的回收率,以量化来自奶油蜜露蜂蜜的肽。通过进一步互补的蛋白质分析(SDS-PAGE)来支持质谱中的唯一性和高响应。所选标记肽Ealphvpifdr(MRJP 1),Ilganvk(MRJP 2),TFVTIER(MRJP 3),QNIDVVAR(MRJP 4),FINNDYNFNEVNFR(MRJP 5)和LLQPYPDWSWTK(MRJP 7),由LC-QQQ-MS / MS量化,强调MRJP 4的QNIDVVAR的内容可用于将蜂蜜蜜露从花卉蜂蜜(P <0.05)分化为其认证的潜在标记。最后,主要成分分析突出显示QnidVVAR内容作为分析的蜜露蜂蜜样品的良好描述符。

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