期刊
PROTEOMICS
卷 12, 期 3, 页码 380-390出版社
WILEY
DOI: 10.1002/pmic.201000726
关键词
Affinity chromatography; Magnetic nanoparticles; Mass spectrometry; Phosphoproteomics; Technology
资金
- National Science Council (NSC) of Taiwan, Republic of China [99-2113-M-260-001-MY2, 97-2113-M-260-004-MY2]
Titanium dioxide (TiO2) has been widely used for phosphopeptide enrichment. Several approaches have been reported to produce magnetic TiO2 affinity probes. In this report, we present a facile approach to immobilize TiO2 onto poly(acrylic acid)-functionalized magnetic carbon-encapsulated iron nanoparticles as affinity probes for efficient enrichment of phosphopeptides. By using the new magnetic TiO2 affinity probes, denoted as TiO2-coated Fe@CNPs, rapid and effective MALDI-TOF MS profiling of phosphopeptides was demonstrated in different model systems such as tryptic digests of beta-casein, and complex beta-casein/BSA mixture. The TiO2-coated Fe@CNPs out-performed the commercial TiO2-coated magnetic beads for detection of phosphopeptides from tryptic digests of beta-casein/BSA mixture with a molar ratio of 1:100. The new TiO2-coated magnetic probes were also proven to be applicable for real life samples. The magnetic TiO2-coated Fe@CNPs were employed to selectively isolate phosphopeptides from tryptic digests of HeLa cell lysates and out-performed the commercial magnetic TiO2 beads in the number of identified phosphopeptides and phosphorylation sites. In a 200-mu g equivalent of HeLa cell lysates, we identified 1415 unique phosphopeptides and 1093 phosphorylation sites, indicating the good performance of the new approach.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据