Qu S, Barrett-Wilt G, Fonseca L M, Rankin S A
Department of Food Science, Mass Spectrometry/Proteomics Facility, University of Wisconsin-Madison 53706.
Biotechnology Center, Mass Spectrometry/Proteomics Facility, University of Wisconsin-Madison 53706.
J Dairy Sci. 2016 Jul;99(7):5083-5092. doi: 10.3168/jds.2015-10431. Epub 2016 Apr 13.
This work characterized a fraction of constituents in yak milk within the realm of approximately 1,000 to 3,000 Da using matrix-assisted laser desorption/ionization (MALDI) time-of-flight mass spectrometry. Eleven samples of yak milk powder from the Sichuan province of China were received by the Department of Food Science, University of Wisconsin-Madison, and stored at room temperature until analysis. Sample preparation involved delipidation and deproteinization of yak milk samples and cold ethanol precipitation. Subsequently, MALDI time-of-flight mass spectrometry was performed in positive ion, reflector mode (AB Sciex TOF/TOF 4800 MALDI; AB Sciex, Foster City, CA). The instrument was first calibrated with the manufacturer's 6-peptide mixture, and each spectrum was internally calibrated using the accurate mass of ACTH Fragment 18-39 standard peptide (protonated mass at m/z 2464.199) present in each sample. Laser power was adjusted for the calibration standards and for each sample so that the signal obtained for the most-abundant ion in each spectrum could be maximized, or kept below ~2×10(4) to preserve spectral quality. Structure and name based on mass were matched using the Metlin metabolite database (https://metlin.scripps.edu/index.php). Results of the current work for yak milk powder showed a large variety of sphingolipid structures with clusters around 1,200, 1,600, and 2,000 Da. The profiling matched several glycosphingolipids, such as gangliosides GA1, GD1a, GD1b, GD3, GM1, GM2, GM3, and GT2 and several other unique moieties, including deaminated neuraminic acid (KDN) oligosaccharides, and fucose containing gangliosides. Matrix preparation and MALDI time-of-flight parameters were important factors established in this work to allow high resolution profiling of complex sphingolipids in yak powder milk.
本研究利用基质辅助激光解吸/电离(MALDI)飞行时间质谱,对牦牛奶中分子量约为1000至3000道尔顿范围内的部分成分进行了表征。美国威斯康星大学麦迪逊分校食品科学系收到了来自中国四川省的11份牦牛奶粉样本,并在室温下储存直至分析。样品制备包括牦牛奶样本的脱脂、脱蛋白以及冷乙醇沉淀。随后,在正离子反射模式下进行MALDI飞行时间质谱分析(AB Sciex TOF/TOF 4800 MALDI;AB Sciex,美国加利福尼亚州福斯特城)。该仪器首先用制造商的6肽混合物进行校准,并且每个样本的光谱都使用每个样本中存在的促肾上腺皮质激素片段18 - 39标准肽(质子化质量为m/z 2464.199)的精确质量进行内部校准。针对校准标准品和每个样本调整激光功率,以使每个光谱中最丰富离子获得的信号最大化,或保持在约2×10⁴以下以保持光谱质量。基于质量的结构和名称使用Metlin代谢物数据库(https://metlin.scripps.edu/index.php)进行匹配。当前对牦牛奶粉的研究结果显示出多种鞘脂结构,在1200、1600和2000道尔顿左右有聚类。该图谱与几种糖鞘脂相匹配,如神经节苷脂GA₁、GD₁a、GD₁b、GD₃、GM₁、GM₂、GM₃和GT₂,以及其他几种独特的部分,包括脱氨基神经氨酸(KDN)寡糖和含岩藻糖的神经节苷脂。基质制备和MALDI飞行时间参数是本研究中确定的重要因素,以实现对牦牛奶粉中复杂鞘脂的高分辨率分析。