School of Food and Biological Engineering, Jiangsu University, Zhenjiang, Jiangsu 212013, PR China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2013 Feb 1;915-916:33-8. doi: 10.1016/j.jchromb.2012.12.013. Epub 2012 Dec 25.
Functional immobilized metal affinity magnetic carboxymethyl chitosan nanoparticles (abbreviated as Fe(3)O(4) (PEG+CM-CTS) @ Fe (III)) were conveniently applied for phosvitin phosphopeptides (PPPs) enrichment for the first time. The morphology of magnetic nanoparticles was observed by transmission electron microscope (TEM). It was found that the diameter of Fe(3)O(4) (PEG+CM-CTS) @ Fe (III) was about 20 nm, and could easily aggregate by a magnet when suspending in the aqueous solution. In the PPPs enrichment study, the results obtained emphasized the role of pH, temperature and the initial concentration of the peptides solution in governing the efficiency and mechanism of affinity interactions. Due to the large specific surface area, the enrichment of PPPs onto the Fe(3)O(4) (PEG+CM-CTS) @ Fe (III) nanoparticles was promising. The adsorption equilibrium of PPPs onto the obtained magnetic nanoparticles fitted well with the Langmuir model, and the nitrogen/phosphorus molar ratio (N/P) which at the maximum enrichment capacity for PPPs was 4.83. Due to the small diameter, the decrease of the N/P is particularly rapid in the early enrichment stages (0-30 min) to reach a plateau after 60 min. Compared with traditional methods, the need for preparation of phosvitin before purification is obviated and PPPs of higher purity were obtained. Since the preparation, surface modification and affinity separation processes of the magnetic nanoparticles are cost-effective, convenient and efficient, this type of Fe(3)O(4) (PEG+CM-CTS) @ Fe (III) nanoparticles would bring advantages compared to conventional separation techniques of PPPs from chicken egg yolk, as well as for phosphopeptides enrichment in proteomics research.
功能化固定化金属亲和磁性羧甲基壳聚糖纳米粒子(简称 Fe(3)O(4)(PEG+CM-CTS)@Fe(III))首次被方便地应用于卵黄高磷蛋白磷酸肽(PPPs)的富集。通过透射电子显微镜(TEM)观察磁性纳米粒子的形态。结果发现,Fe(3)O(4)(PEG+CM-CTS)@Fe(III)的直径约为 20nm,在水溶液中悬浮时,很容易通过磁铁聚集。在 PPPs 富集研究中,得到的结果强调了 pH 值、温度和肽溶液初始浓度在控制亲和相互作用效率和机制中的作用。由于具有较大的比表面积,Fe(3)O(4)(PEG+CM-CTS)@Fe(III)纳米粒子对 PPPs 的富集效果良好。PPPs 吸附平衡在实验得到的磁性纳米粒子上较好地符合朗缪尔模型,最大 PPPs 富集容量的氮/磷摩尔比(N/P)为 4.83。由于直径较小,在早期富集阶段(0-30min),N/P 迅速下降,60min 后达到平台。与传统方法相比,该方法在纯化前不需要制备卵黄高磷蛋白,得到的 PPPs 纯度更高。由于磁性纳米粒子的制备、表面修饰和亲和分离过程具有成本效益、方便高效的特点,与传统的从鸡卵黄中分离 PPPs 的分离技术相比,以及在蛋白质组学研究中用于磷酸肽的富集,这种 Fe(3)O(4)(PEG+CM-CTS)@Fe(III)纳米粒子将具有优势。