Department of Pharmacy, University of Naples Federico II, Napoli, Italy.
Department of Pharmacy, University of Salerno, Fisciano, SA, Italy; PhD Program in Drug Discovery and Development, University of Salerno, Fisciano, SA, Italy.
J Pharm Biomed Anal. 2019 Oct 25;175:112783. doi: 10.1016/j.jpba.2019.112783. Epub 2019 Jul 19.
In this study, a comprehensive hydrophilic interaction chromatography × reversed phase coupled to high resolution mass spectrometry was developed for the peptide profile of microalgae formulations subjected to gastro-intestinal digestion. A BEH Amide column was employed in the first dimension, while a BIOshell ES-C18 Peptide in the second. As modulation interface, two trapping columns, in house packed with 1.9 μm fully porous monodisperse C18 particles characterized by high retention and efficiency, were tested and compared with SecurityGuard C18 cartridges, together with a dilution flow, to reduce first dimension mobile phase strength. The platform was coupled to both diode array detector and Orbitrap mass spectrometry. The developed setup provided high peak capacity (n: 957) in only 60 min and a good orthogonality (A: 0.70). The employment of the custom made C18 traps resulted in improved sensitivity (signal enhancement = 4) and a higher number of peptides detected (+58) especially of short lenght (≤ 6 aminoacids), with respect to the setup based on the security guard C18 traps. 184 phycocyanin-derived peptides were detected in Klamath and Spirulina gastro-intestinal digests, whose sequence and protein origin has been elucidated in detail by mass spectrometry. The results show the potential of the developed HILIC × RP-MS platform for in depth peptide mapping of microalgae and its possible application to highlight the products of gastro-intestinal digestion of other microalgae species.
本研究建立了一种综合亲水作用色谱-反相高效液相色谱-高分辨质谱联用方法,用于分析经胃肠消化的微藻制剂的肽谱。在第一维中采用 BEH Amide 柱,在第二维中采用 BIOshell ES-C18 Peptide 柱。作为调制接口,我们测试了两个填充有 1.9 µm 全多孔单分散 C18 颗粒的自制捕集柱,并与 SecurityGuard C18 柱进行了比较,同时采用稀释流来降低第一维流动相强度。该平台与二极管阵列检测器和 Orbitrap 质谱仪联用。所建立的方法在仅 60 分钟内实现了高峰容量(n:957)和良好的正交性(A:0.70)。使用定制的 C18 捕集柱可提高灵敏度(信号增强=4)和检测到的肽数量(增加+58),特别是短长度(≤6 个氨基酸)的肽,这与基于 SecurityGuard C18 捕集柱的方法相比。在克拉马斯和螺旋藻胃肠消化物中检测到 184 个藻蓝蛋白衍生肽,通过质谱详细阐明了它们的序列和蛋白质来源。结果表明,所开发的亲水作用色谱-反相高效液相色谱-高分辨质谱联用平台在微藻的深入肽谱分析中具有潜力,并可能应用于突出其他微藻物种胃肠消化产物。