Rapid enrichment of phosphopeptides and phosphoproteins from complex samples using magnetic particles coated with alumina as the concentrating probes for MALDI MS analysis

被引:133
|
作者
Chen, Cheng-Tai
Chen, Wei-Yu
Tsai, Pei-Jane
Chien, Kun-Yi
Yu, Jau-Song
Chen, Yu-Chie [1 ]
机构
[1] Natl Chiao Tung Univ, Dept Appl Chem, Hsinchu 300, Taiwan
[2] Natl Chiao Tung Univ, Inst Mol Sci, Hsinchu 300, Taiwan
[3] Tzu Chi Univ, Dept Lab Med & Biotechnol, Hualien 970, Taiwan
[4] Chang Gung Univ, Chang Gung Proteom Core Lab, Dept Biochem, Tao Yuan, Taiwan
[5] Chang Gung Univ, Dept Cell & Mol Biol, Grad Inst Basic Med Sci, Tao Yuan, Taiwan
关键词
alumina; magnetic particles; phosphopeptides; phosphoproteins; MALDI MS;
D O I
10.1021/pr0604460
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In this study, we used nanocomposite magnetic particles coated with alumina as the affinity probes to selectively concentrate phosphorylated peptides and proteins from a low volume of sample solution. Tryptic digest products of phosphoproteins including alpha- and beta-caseins, human protein phosphatase inhibitor 1, nonfat milk, egg white, and a cell lysate were used as the samples to demonstrate the feasibility of this approach. In only 30 and 90 s, phosphopeptides and phosphoproteins sufficient for characterization by MALDI-MS were enriched by the particles, respectively. Proteins trapped on the particles could be directly digested on the particles. The same particles in the digest solution were employed for enrichment of phosphopeptides. We estimated the required time for performing the enrichment of phosphopeptides from complex samples and characterization by MALDI MS was within 5 min. A small volume (50 mu L) and a low concentration (5 x 10(-10) M) of tryptic digest product of a phosphoprotein sample could be dramatically enriched and characterized using this approach.
引用
收藏
页码:316 / 325
页数:10
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