Weng Wei-Chien, Liao Hung-En, Chang Cheng-Hsiu, Hung Shang-Cheng, Du Kai, Tu Zhijay, Lin Chun-Hung, Ni Chi-Kung
Institute of Atomic and Molecular Sciences, Academia Sinica, Taipei, 106216, Taiwan.
Molecular Science and Technology, International Graduate Program, Department of Chemistry, Academia Sinica, National Tsing Hua University, Hsinchu, 300044, Taiwan.
Sci Rep. 2025 Jan 10;15(1):1586. doi: 10.1038/s41598-024-81561-1.
Free oligosaccharides in human milk have many biological functions for infant health. The reducing end of most human milk oligosaccharides is lactose, and caprine milk was reported to contain oligosaccharides structurally similar to those present in human milk. The structures of oligosaccharides were traditionally determined using nuclear magnetic resonance spectroscopy or enzyme digestion followed by various detection methods, e.g., liquid. Mass spectrometry has much higher sensitivity than nuclear magnetic resonance spectroscopy and enzyme digestion. However, conventional mass spectrometry methods only determine part of the structures of oligosaccharides, i.e., compositions and linkage positions. In this study, we used the latest developed mass spectrometry method, namely logically derived sequence tandem mass spectrometry, to determine the complete structures (i.e., composition, linkage positions, anomericities, and stereoisomers) of free neutral trisaccharides in caprine colostrum and mature milk. The high sensitivity of mass spectrometry enables us to discover oligosaccharides of low abundance. Isomers of (Hex)HexNAc, (Hex), and (Hex)Fuc which have not been reported before were identified. Many of them do not have lactose at the reducing end. Instead, the reducing end is either Glcβ-(1-4)-Glc or Glcβ-(1-4)-GlcNAc. These unusual oligosaccharides are higher in concentration and more structurally diverse in caprine colostrum than that in caprine mature milk and human milk. The structural diversity indicates more complicated biosynthetic pathways of caprine milk compared to that of human milk.
人乳中的游离寡糖对婴儿健康具有多种生物学功能。大多数人乳寡糖的还原端是乳糖,据报道山羊乳中含有结构与人乳中相似的寡糖。传统上,寡糖的结构是使用核磁共振光谱法或酶消化后再结合各种检测方法(如液相色谱法)来确定的。质谱分析法比核磁共振光谱法和酶消化法具有更高的灵敏度。然而,传统的质谱分析法只能确定寡糖结构的一部分,即组成和连接位置。在本研究中,我们使用最新开发的质谱分析法,即逻辑推导序列串联质谱法,来确定山羊初乳和成熟乳中游离中性三糖的完整结构(即组成、连接位置、异头物和立体异构体)。质谱分析法的高灵敏度使我们能够发现低丰度的寡糖。我们鉴定出了之前未报道过的(己糖)己糖胺、(己糖)和(己糖)岩藻糖的异构体。其中许多在还原端没有乳糖。相反,还原端要么是Glcβ-(1-4)-Glc,要么是Glcβ-(1-4)-GlcNAc。这些不寻常的寡糖在山羊初乳中的浓度更高,结构也比山羊成熟乳和人乳更多样化。这种结构多样性表明,与人类乳汁相比,山羊乳的生物合成途径更为复杂。