Kim Bum Jin, Dallas David C
Nutrition Program, School of Biological and Population Health Sciences, College of Public Health and Human Sciences, Oregon State University, Corvallis, OR, 97331, USA.
Nutrition Program, School of Biological and Population Health Sciences, College of Public Health and Human Sciences, Oregon State University, Corvallis, OR, 97331, USA.
Talanta. 2021 Mar 1;224:121811. doi: 10.1016/j.talanta.2020.121811. Epub 2020 Oct 27.
Human milk contains numerous N-glycoproteins with functions that provide protection to the infant. Increasing understanding of the functional role of human milk glycoproteins within the infant requires toolsets to comprehensively profile their site-specific glycosylation patterns. However, optimized methods for site-specific glycosylation analysis across the entire human milk proteome are not available. Therefore, we performed a systematic analysis of techniques for profiling the sites and compositions of N-glycans in human milk using liquid chromatography/mass spectrometry. To decrease interference from non-target molecules, we compared techniques for protein extraction, including ethanol (EtOH) precipitation, trichloroacetic acid precipitation, molecular weight cut-off filtration and techniques for tryptic glycopeptide enrichment, including C18-, porous graphitized carbon and hydrophilic interaction liquid chromatography (HILIC)-solid phase extraction (SPE) and acetone precipitation. We compared the capacity of higher-energy collision dissociation, electron-transfer dissociation and electron-transfer/higher-energy collision dissociation (EThcD) to produce fragment ions that would enable effective identification of the glycan composition, peptide sequence and glycosylation site. Of these methods, a combination of EtOH precipitation, HILIC-SPE and EThcD-fragmentation was the most effective for human milk N-glycopeptide profiling. This optimized approach significantly increased the number of N-glycopeptides and precursor N-glycoproteins (246 N-glycopeptides from 29 glycoproteins) compared with a more common extraction approach with no protein extraction and C18 clean-up (62 N-glycopeptides from 11 glycoproteins). The advancement in methods for human milk N-glycoproteins provided by this study represents a key step for better understanding the function of glycoproteins within the breast milk-fed infant.
母乳中含有众多具有保护婴儿功能的N - 糖蛋白。要深入了解母乳糖蛋白在婴儿体内的功能作用,需要有工具集来全面描绘其位点特异性糖基化模式。然而,目前尚无针对整个人乳蛋白质组进行位点特异性糖基化分析的优化方法。因此,我们利用液相色谱/质谱对母乳中N - 聚糖的位点和组成进行分析的技术进行了系统研究。为减少非目标分子的干扰,我们比较了蛋白质提取技术,包括乙醇(EtOH)沉淀、三氯乙酸沉淀、分子量截留过滤,以及胰蛋白酶糖肽富集技术,包括C18、多孔石墨化碳和亲水相互作用液相色谱(HILIC) - 固相萃取(SPE)和丙酮沉淀。我们比较了高能碰撞解离、电子转移解离和电子转移/高能碰撞解离(EThcD)产生能够有效鉴定聚糖组成、肽序列和糖基化位点的碎片离子的能力。在这些方法中,乙醇沉淀、HILIC - SPE和EThcD - 碎片化的组合对人乳N - 糖肽分析最为有效。与更常见的不进行蛋白质提取和C18净化的提取方法(11种糖蛋白中的62种N - 糖肽)相比,这种优化方法显著增加了N - 糖肽和前体N - 糖蛋白的数量(29种糖蛋白中的246种N - 糖肽)。本研究提供的人乳N - 糖蛋白分析方法的进步是更好理解母乳喂养婴儿体内糖蛋白功能的关键一步。