色谱
色譜
색보
CHINESE JOURNAL OF CHROMATOGRAPHY
2014年
4期
369-375
,共7页
液相色谱%质谱%富集%糖蛋白%凝集素%磁性纳米粒子
液相色譜%質譜%富集%糖蛋白%凝集素%磁性納米粒子
액상색보%질보%부집%당단백%응집소%자성납미입자
liquid chromatography( LC)%mass spectrometry( MS)%enrichment%glycopro-tein%lectin%magnetic nanoparticle
发展了一种新型的磁性纳米粒子应用于人血清中特异性糖蛋白的亲和富集。制备的磁性纳米粒子具有核/壳/壳结构,即由 Fe3 O4磁性粒子/硅胶层/有机聚合物外层构成。伴刀豆凝集素 A(Con A)以共价键合的形式通过短链聚乙二醇固定在粒子表面,实现了人血清中特异性糖蛋白的高效富集。富集的蛋白经过胰蛋白酶酶解后,所得的肽段经离线的二维色谱分离,用高分辨质谱共鉴定出80种蛋白。通过 NetNGlyc 等搜索软件分析确定其中76种为糖蛋白,分析发现在血清中质量浓度仅为0.00001 g / L 的β-2-glycoprotein 1也得到了鉴定,表明我们发展的磁性纳米粒子与凝集素相结合的方式,可以高效地富集复杂体系中与主要蛋白成分含量相差12个数量级的低丰度糖蛋白。
髮展瞭一種新型的磁性納米粒子應用于人血清中特異性糖蛋白的親和富集。製備的磁性納米粒子具有覈/殼/殼結構,即由 Fe3 O4磁性粒子/硅膠層/有機聚閤物外層構成。伴刀豆凝集素 A(Con A)以共價鍵閤的形式通過短鏈聚乙二醇固定在粒子錶麵,實現瞭人血清中特異性糖蛋白的高效富集。富集的蛋白經過胰蛋白酶酶解後,所得的肽段經離線的二維色譜分離,用高分辨質譜共鑒定齣80種蛋白。通過 NetNGlyc 等搜索軟件分析確定其中76種為糖蛋白,分析髮現在血清中質量濃度僅為0.00001 g / L 的β-2-glycoprotein 1也得到瞭鑒定,錶明我們髮展的磁性納米粒子與凝集素相結閤的方式,可以高效地富集複雜體繫中與主要蛋白成分含量相差12箇數量級的低豐度糖蛋白。
발전료일충신형적자성납미입자응용우인혈청중특이성당단백적친화부집。제비적자성납미입자구유핵/각/각결구,즉유 Fe3 O4자성입자/규효층/유궤취합물외층구성。반도두응집소 A(Con A)이공개건합적형식통과단련취을이순고정재입자표면,실현료인혈청중특이성당단백적고효부집。부집적단백경과이단백매매해후,소득적태단경리선적이유색보분리,용고분변질보공감정출80충단백。통과 NetNGlyc 등수색연건분석학정기중76충위당단백,분석발현재혈청중질량농도부위0.00001 g / L 적β-2-glycoprotein 1야득도료감정,표명아문발전적자성납미입자여응집소상결합적방식,가이고효지부집복잡체계중여주요단백성분함량상차12개수량급적저봉도당단백。
Biomedical sciences,and in particular biomarker research,demand efficient glyco-protein enrichment platforms. Herein novel magnetic nanoparticles with an average size around 135 nm in diameter were prepared for the enrichment of glycoproteins in human serum. The prepared magnetic nanoparticles possessed uniform core / shell / shell structure which was com-posed of 8 nm magnetite internal core and double layers consisting of silica and poly glycidyl methacrylate(GMA). The latter was constructed by seed polymerization. Modified by a poly-ethylene hydrophilic linker,it made the surfaces of the magnetic nanoparticles highly hydrophil-ic so as to reduce the nonspecific adsorption of proteins. We examined affinity purification of glycoprotein in diluted human serum using our prepared magnetic nanoparticles with immobi-lization of concanavalin A( MNP@ ConA). The enriched proteins were reduced,alkylated and digested with trypsin. These peptides then were separated by offline two-dimensional chroma-tography. Protein identification was realized with nano-high performance liquid chromatogra-phy-orbitrap mass spectrometry. A total of 80 proteins were identified,among them 76 proteins were found to be glycoproteins by use of bioinformatic tools. β-2-Glycoprotein 1 present in ser-um at low mass concentration around 0. 000 01 g / L was also identified. This demonstrates the capability of magnetic nanoparticle for recovering minute amounts of glycoproteins from a fluid exhibiting a dynamic concentration range more than 12 orders of magnitude. Overall,MNP@ConA has been proven to be an efficient alternative to currently available immobilization supports.