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首页> 外文期刊>Analytical and bioanalytical chemistry >Identification of bioactive short peptides in cow milk by high-performance liquid chromatography on C18 and porous graphitic carbon coupled to high-resolution mass spectrometry
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Identification of bioactive short peptides in cow milk by high-performance liquid chromatography on C18 and porous graphitic carbon coupled to high-resolution mass spectrometry

机译:高效液相色谱法鉴定牛奶中的生物活性短肽和高孔石墨碳耦合到高分辨率质谱法

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Short peptides are important compounds in a variety of fields, including food and nutraceutical applications, but also biomarker discovery, bioactive peptide discovery and peptide drug separation. Despite the importance of short peptides, they are currently less studied than other peptides because of the lack of dedicated methods for their characterization. The method described in this paper comprises a combination of strategies to tackle the main limitations in short peptide analysis. In particular, in this work an untargeted peptidomic approach based on ultrahigh-performance liquid chromatography coupled to high-resolution mass spectrometry was developed for the identification of short peptides in cow milk samples. After milk defatting and precipitation, the sample was purified by cotton-hydrophilic interaction liquid chromatography (HILIC) micro tip in order to avoid suppression phenomena due to contaminants present in milk, such as carbohydrates. The sample was then separated by means of two chromatographic columns, with a complementary selectivity mechanism, namely reversed-phase C18 column and porous graphitic carbon (PGC). By this approach, the method allowed the separation and characterization of di-, tri- and tetrapeptides. A total of 57 and 41 peptides were identified by using a C18 and a PGC column, respectively; in particular, 31 were exclusively identified by using the C18 column, 15 unique peptides were identified by using the PGC column, while 26 were in common between the two data sets, demonstrating that the two columns have a different selectivity mechanism. The results indicated that an integrated approach may be appropriate to improve the separation of different peptides and increase the number of identifications because of the wide range of polarity of short peptides. The method allowed the untargeted identification of short peptides in milk, a complex matrix chosen as a representative real sample for method application, and provides complementa
机译:短肽是各种领域的重要化合物,包括食品和营养保健型应用,但也是生物标志物发现,生物活性肽发现和肽药物分离。尽管肽短肽的重要性,但由于缺乏专用方法,它们目前比其他肽在其特征中缺乏缺乏。本文描述的方法包括在短肽分析中解决主要限制的策略组合。特别地,在这项工作中,基于耦合到高分辨率质谱的超高性能液相色谱法的未标准肽肽方法用于鉴定牛奶样品中的短肽。在牛奶脱落和沉淀后,通过棉 - 亲水相互作用液相色谱(HILIC)微尖来纯化样品,以避免由于牛奶中存在的污染物,例如碳水化合物而抑制现象。然后通过两个色谱柱分离样品,具有互补的选择性机制,即反相C18柱和多孔石墨碳(PGC)。通过这种方法,该方法允许分离和表征二肽的分离和表征。通过使用C18和PGC柱鉴定总共57和41个肽;特别地,通过使用C18柱专门鉴定31,通过使用PGC塔来鉴定15个独特的肽,而26在两个数据集之间有共同,表明两列具有不同的选择性机制。结果表明,由于短肽的各种极性,综合方法可以适当地改善不同肽的分离并增加鉴定的数量。该方法允许牛奶中的短肽未确定鉴定,选择作为方法应用的代表实际样品的复杂基质,并提供互补

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