Chen Cheng-Tai, Chen Wei-Yu, Tsai Pei-Jane, Chien Kun-Yi, Yu Jau-Song, Chen Yu-Chie
Department of Applied Chemistry and Institute of Molecular Science, National Chiao Tung University, Hsinchu 300, Taiwan.
J Proteome Res. 2007 Jan;6(1):316-25. doi: 10.1021/pr0604460.
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 microL) 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.
在本研究中,我们使用涂有氧化铝的纳米复合磁性颗粒作为亲和探针,从少量样品溶液中选择性富集磷酸化肽和蛋白质。以包括α-酪蛋白和β-酪蛋白、人蛋白磷酸酶抑制剂1、脱脂牛奶、蛋清和细胞裂解液在内的磷蛋白的胰蛋白酶消化产物作为样品,以证明该方法的可行性。仅在30秒和90秒内,颗粒就分别富集了足以通过基质辅助激光解吸电离质谱(MALDI-MS)进行表征的磷酸肽和磷蛋白。捕获在颗粒上的蛋白质可直接在颗粒上进行消化。消化溶液中的相同颗粒用于富集磷酸肽。我们估计,从复杂样品中富集磷酸肽并通过MALDI MS进行表征所需的时间在5分钟以内。使用这种方法,可以显著富集和表征小体积(50微升)和低浓度(5×10⁻¹⁰ M)的磷蛋白样品的胰蛋白酶消化产物。