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含钛磁性介孔硅球:有效富集肽并同时分离非磷酸化肽和磷酸化肽。

Titanium-containing magnetic mesoporous silica spheres: effective enrichment of peptides and simultaneous separation of nonphosphopeptides and phosphopeptides.

机构信息

Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), Department of Chemistry, Wuhan University, Wuhan, P R China.

出版信息

J Sep Sci. 2012 Jun;35(12):1506-13. doi: 10.1002/jssc.201101067.

DOI:10.1002/jssc.201101067
PMID:22740261
Abstract

Protein phosphorylation is a common posttranslational modification, and involved in many cellular processes. Like endogenous peptides, endogenous phosphopeptides contain many biomarkers of preclinical screening and disease diagnosis. In this work, titanium-containing magnetic mesoporous silica spheres were synthesized and applied for effective enrichment of peptides from both tryptic digests of standard proteins and human serum. Besides, the enriched peptides can be further separated into nonphosphopeptides and phosphopeptides by a simple elution. First, titanium-containing magnetic mesoporous silica spheres were synthesized by a sol-gel method and found to have high surface area, narrow pore size distribution, and useful magnetic responsivity. Then, as the prepared material was used for selective capturing of phosphopeptides, it demonstrated to have higher selectivity than commercial titanium dioxide. Moreover, via combination of size-exclusion mechanism, hydrophobic interaction, and affinity chromatography, titanium-containing magnetic mesoporous silica spheres were successfully applied to simultaneously extract and separate nonphosphopeptides and phosphopeptides from standard protein digestion and human serum.

摘要

蛋白质磷酸化是一种常见的翻译后修饰,参与许多细胞过程。与内源性肽一样,内源性磷酸肽包含许多临床前筛选和疾病诊断的生物标志物。在这项工作中,合成了含钛磁性介孔硅球,并将其应用于有效富集标准蛋白和人血清胰蛋白酶消化物中的肽。此外,通过简单的洗脱,富集的肽可进一步分离为非磷酸肽和磷酸肽。首先,通过溶胶-凝胶法合成了含钛磁性介孔硅球,发现其具有高比表面积、窄孔径分布和有用的磁响应性。然后,由于所制备的材料用于选择性捕获磷酸肽,其表现出比商业二氧化钛更高的选择性。此外,通过排阻机制、疏水相互作用和亲和层析的结合,含钛磁性介孔硅球成功地应用于从标准蛋白消化物和人血清中同时提取和分离非磷酸肽和磷酸肽。

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引用本文的文献

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Electrophoresis. 2014 Dec;35(24):3418-29. doi: 10.1002/elps.201400017. Epub 2014 Jun 16.