Department of Chemical Engineering, National Taiwan University of Science and Technology, 43 Keelung Rd Sec. 4, Taipei 106, Taiwan.
ACS Appl Mater Interfaces. 2011 Sep;3(9):3342-9. doi: 10.1021/am200453e. Epub 2011 Aug 23.
Magnetic nanoparticles (MNPs) with an amine functionalized surface (MH) were passivated with carbonaceous materials (MH@C) by carbonization of glucose under hydrothermal reaction conditions. The carboxylate groups in carbonaceous shell could be enriched to 0.285 mmol/g when acrylic acid was added as a functional monomer in the carbonization reaction (MH@C-Ac). The carbonaceous shell not only protected the magnetic core from acidic erosion but also showed a high adsorption capacity toward Ni(2+) ion. The Ni(2+) ion complexed on MH@C and MH@C-Ac could specifically isolate 6×His tagged recombinant proteins from crude bacterial extracts via metal affinity interaction. The superparamagnetic property facilitates the easy retrieval of the carbonaceous material passivated MNPs from the viscous proteins solutions. Recombinant green fluorescence protein (GFP) and hyaluronic acid (HA) lyase of 9.4 mg and 2.3 mg could be isolated by 1 g of MH@C-Ac-Ni, respectively.
通过在水热反应条件下将葡萄糖碳化,使表面带有胺官能团的磁性纳米颗粒 (MNPs) (MH) 被碳化材料 (MH@C) 钝化。当在碳化反应中添加丙烯酸作为功能单体时,碳壳中的羧酸基团可以富集到 0.285mmol/g(MH@C-Ac)。碳壳不仅可以保护磁核免受酸性侵蚀,而且对 Ni(2+) 离子表现出高吸附能力。MH@C 和 MH@C-Ac 上的 Ni(2+) 离子配合物可以通过金属亲和相互作用,从粗细菌提取物中特异性分离出 6×His 标记的重组蛋白。超顺磁性使得易于从粘性蛋白质溶液中回收被碳质材料钝化的 MNPs。通过 1g 的 MH@C-Ac-Ni,可以分别分离出 9.4mg 的重组绿色荧光蛋白 (GFP) 和 2.3mg 的透明质酸 (HA) 裂解酶。