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琼脂糖-玻璃珠亲和色谱填料合成及分离应用 被引量:1

Preparation of agarose-glass composite particles for affinity purification of glycoproteins
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摘要 利用油水乳化法,制备具有壳-核结构的琼脂糖/玻璃珠复合材料,并偶联氨基苯硼酸,得到一种新型的亲和填料。对影响制备过程的琼脂糖/玻璃珠质量比、乳化剂的含量、环氧基团活化密度进行了优化。采用光学显微镜、激光粒度分析仪、红外光谱仪、热质量分析仪等对这种复合介质进行了表征,并考察亲和介质的吸附性能。结果表明:复合材料对辣辣根过氧化物酶(糖蛋白)的饱和吸附量为85 mg/g,远大于牛血清蛋白(非糖蛋白)6 mg/g的吸附量,并在2 mL/min流速下实现了对人血红细胞中糖化血红蛋白与非糖化血红蛋白的分离,在亲和色谱方面具有较大的应用前景。 M-aminophenyboronic acid( APBA)-functionalized agarose-glass composite particles were fabricated by water-in-oil emulsification for a specific affinity to glycoproteins. The reaction conditions were optimized,including the ratio of agarose to glass,the content of emulsifier and epichlorohydrin( ECH). The affinity particles were characterized by optical microscope,laser particle size analyzer, Fourier transform infrared spectroscopy( FT-IR),and thermogravimetry( TG). The saturated adsorption capacity of horse radish peroxidase( HRP) was 85 mg / g,which was remarkably higher than that obtained for bovine serum albumin( BSA). It could be applied to the specific capture of the glycosylated hemoglobin at 2 mL / min in chromatography with a potential application in affinity chromatography.
出处 《南京工业大学学报(自然科学版)》 CAS 北大核心 2014年第3期82-88,共7页 Journal of Nanjing Tech University(Natural Science Edition)
关键词 油水乳化 复合材料 琼脂糖 氨基苯硼酸 糖蛋白 water-in-oil emulsification composite particles agarose m-aminophenyboronic acid(APBA) glycoprotein
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  • 1甄宇红,杨青,张宝.环氧氯丙烷法活化琼脂糖凝胶及其动力学分析[J].大连医科大学学报,2005,27(4):268-272. 被引量:10
  • 2穆成华,姚红娟,马光辉,连宾.肝素-琼脂糖凝胶6FF的制备及其在抗凝血酶III分离纯化中的应用[J].过程工程学报,2005,5(5):545-549. 被引量:9
  • 3Ueda E K M, Gout P W, Morganti L. Current and Prospective Applications of Metal Ion-Protein Binding [J]. J. Chromatogr. A, 2003, 988(1): 1-23.
  • 4Sousal F, Prazeres D M F, Queiroz J A. Affinity Chromatography Approaches to Overcome the Challenges of Purifying Plasmid DNA [J]. Trends Biotechnol., 2008, 26(9): 518-525.
  • 5Azarkan M, Huet J, Baeyens-Volant D, et al. Affinity Chromatography: A Useful Tool in Proteomics Studies [J]. J. Chromatogr. B, 2007, 849(1/2): 81-90.
  • 6Jungbauer A, Kaar W, Schlegl R. Folding and Refolding of Proteins in Chromatographic Beds [J]. Curr. Opin. Biotechnol., 2004, 15(5): 487-494.
  • 7General Electric Healthcare Company. GE Healthcare Data file [EB/OL]. http://www.gelifesciences.com/aptrix/upp00919.ns f/, Content/0DDCOCC415DCCB68C 1257628001D29A9/$file/2840410 6AB.pdf, 2009-03-01.
  • 8Matsumoto I, Mizuno Y, Seno N. Activation of Sepharose with Epichlorohydrin and Subsequent Immobilization of Ligand for Affinity Adsorbent [J]. J. Biochem., 1979, 85(4): 1091-1098.
  • 9Scoble J A, Scopes R K. Assay for Determining the Number of Reactive Groups on Gels Used in Affinity Chromatography and Its Application to the Optimization of the Epichlorohydrin and Divinylsulfone Activation Reactions [J]. J. Chromatogr. A, 1996, 752(1/2): 67-76.
  • 10Shi Q H, Tian Y, Dong X Y, et al. Chitosan-coated Silica Beads as Immobilized Metal Affinity Support for Protein Adsorption [J]. Biochem. Eng. J., 2003, 16(3): 317-322.

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