Zhai Rui, Jiao Fenglong, Feng Duan, Hao Feiran, Li Jiabin, Li Nannan, Yan Hui, Wang Huanhuan, Jin Zuyao, Zhang Yangjun, Qian Xiaohong
College of Life Science and Bio-Engineering, Beijing University of Technology, Beijing, P. R. China; State Key Laboratory of Proteomics, Beijing Proteome Research Center, Beijing Institute of Radiation Medicine, Beijing, P. R. China.
Electrophoresis. 2014 Dec;35(24):3470-8. doi: 10.1002/elps.201400139. Epub 2014 Jul 15.
A new type of mixed lanthanides-immobilized (Tb(3+) , Tm(3+) , Ho(3+) , Lu(3+) ) magnetic nanoparticles, Fe3 O4 @TCPP-DOTA-M(3+) , was prepared with a particle size of approximately 30 nm. A model protein, α-casein, and a protein mixture of α-casein and BSA (1:100) were first used to test the phosphopeptide enrichment efficiency of the newly developed magnetic nanoparticles. For the model protein α-casein, 19 phosphopeptides were identified with the newly developed materials. Even in the tryptic digest of α-casein and BSA (1:100), 16 phosphopeptides were easily detected, suggesting that the novel materials possess high selectivity in phosphopeptide enrichment. To evaluate the phosphopeptide enrichment efficiency in a real biological sample, the materials were used to capture phosphopeptides in the tryptic digests of an extract of HeLa cells. In total, 9048 phosphopeptides corresponding to 2103 phosphoproteins were identified in a single mass spectrometric analysis, indicating the great potential of the new materials for practical applications. Compared with metal oxide-based enrichment methods, the newly developed materials are convenient to prepare and easy to handle, and they save time in the phosphopeptide enrichment procedure, making these materials a good choice for highly selective and sensitive phosphopeptide enrichment in future phosphoproteome analyses.
制备了一种新型的固定化混合镧系元素(Tb(3+)、Tm(3+)、Ho(3+)、Lu(3+))磁性纳米颗粒Fe3O4@TCPP-DOTA-M(3+),其粒径约为30 nm。首先使用一种模型蛋白α-酪蛋白以及α-酪蛋白与牛血清白蛋白(BSA)的蛋白混合物(1:100)来测试新开发的磁性纳米颗粒对磷酸化肽段的富集效率。对于模型蛋白α-酪蛋白,用新开发的材料鉴定出了19个磷酸化肽段。即使在α-酪蛋白与BSA(1:100)的胰蛋白酶消化物中,也能轻松检测到16个磷酸化肽段,这表明该新型材料在磷酸化肽段富集方面具有高选择性。为了评估在实际生物样品中的磷酸化肽段富集效率,将这些材料用于捕获HeLa细胞提取物胰蛋白酶消化物中的磷酸化肽段。在一次质谱分析中,总共鉴定出了与2103个磷酸化蛋白相对应的9048个磷酸化肽段,这表明新材料在实际应用中具有巨大潜力。与基于金属氧化物的富集方法相比,新开发的材料制备方便、易于操作,并且在磷酸化肽段富集过程中节省时间,使其成为未来磷酸化蛋白质组分析中高选择性和高灵敏度磷酸化肽段富集的良好选择。