首页> 美国卫生研究院文献>Journal of Biomolecular Techniques : JBT >Identification on Membrane and Characterization of Phosphoproteins Using an Alkoxide-Bridged Dinuclear Metal Complex as a Phosphate-Binding Tag Molecule
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Identification on Membrane and Characterization of Phosphoproteins Using an Alkoxide-Bridged Dinuclear Metal Complex as a Phosphate-Binding Tag Molecule

机译:使用烷氧基桥接的双核金属配合物作为磷酸结合标签分子对膜的鉴定和磷酸化蛋白的表征

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摘要

We have developed a method for on-membrane direct identification of phosphoproteins, which are detected by a phosphate-binding tag (Phos-tag) that has an affinity to phosphate groups with a chelated Zn2+ ion. This rapid profiling approach for phosphoproteins combines chemical inkjet technology for microdispensing of reagents onto a tiny region of target proteins with mass spectrometry for on-membrane digested peptides. Using this method, we analyzed human epidermoid carcinoma cell lysates of A-431 cells stimulated with epidermal growth factor, and identified six proteins with intense signals upon affinity staining with the phosphate-binding tag. It was already known that these proteins are phosphorylated, and our new approach proved to be effective at rapid profiling of phosphoproteins. Furthermore, we tried to determine their phosphorylation sites by MS/MS analysis after in-gel digestion of the corresponding spots on the 2DE gel to the rapid on-membrane identifications. As one example of use of information gained from the rapid-profiling approach, we successfully characterized a phosphorylation site at Ser-113 on prostaglandin E synthase 3.
机译:我们开发了一种膜上直接鉴定磷蛋白的方法,该方法可以通过磷酸结合标签(Phos-tag)检测,该标签对被螯合的Zn 2 + 离子具有磷酸基团的亲和力。这种针对磷蛋白的快速分析方法结合了化学喷墨技术,可将试剂微分散到目标蛋白的微小区域上,而质谱法则可用于膜上消化的肽。使用这种方法,我们分析了被表皮生长因子刺激的A-431细胞的人表皮样癌细胞裂解液,并用磷酸化结合标签对六种具有强烈信号的蛋白进行了鉴定。已经知道这些蛋白被磷酸化了,我们的新方法被证明对磷蛋白的快速分析有效。此外,我们试图在凝胶内消化2DE凝胶上的相应斑点以快速进行膜上鉴定后,通过MS / MS分析确定其磷酸化位点。作为使用从快速分析方法获得的信息的一个示例,我们成功地表征了前列腺素E合酶3上Ser-113的磷酸化位点。

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