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Preparation and evaluation of lysozyme molecularly imprinted polymer film on the surface of multi-wall carbon nanotubes

机译:多壁碳纳米管表面溶菌酶分子印迹聚合物膜的制备与评价

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Imprinting of macromolecule such as proteins with molecular imprinting technique remains challenge because of their bulkiness, structural complexity and sensitivity of denaturation. The purpose of this study was to synthesize a Lys-MIP film on the surface of the MWNTs by surface molecular imprinting technique, and subsequently selectively recognized and purified Lys from egg white. The Lys-MIP film was prepared using AAm as functional monomer, MBA as cross-linker, APS and TEMED as initiator under the optimized conditions. The polymer was characterized by TEM, FT-IR, TGA, and BET, as well. The equilibrium adsorption experiments and dynamic adsorption experiments were carried out to determine the binding capacity and the equilibrium time. The results showed that adsorption capacity of the Lys-MIP film was 20.89 mg g ~(-1) at 0.50 mg mL ~(-1), and adsorption capacity was 15.37 mg g ~(-1) for the NIP. 82.10% of binging was obtained within 30 min and the adsorption equilibrium was achieved within 300 min. The selectivity adsorption experiments showed the Lys-MIP film had higher affinity and capacity for Lys than that for the competitive proteins, such as Cyt C, Mb, Hb and BSA. The relative selectivity coefficients for Lys/Cyt C, Lys/Mb, Lys/Hb, and Lys/BSA were 1.30, 1.30, 3.12 and 2.82, respectively. Purification experiment of Lys from egg white showed that adsorption capacity of the Lys-MIP film was 1.86 times more than that of the NIP. All these results proved that Lys-MIP film possessed high adsorption capacity and excellent selectivity. This material has great potential for separation of Lys in real samples.
机译:由于分子的体积大,结构复杂和变性敏感性,利用分子印迹技术对诸如蛋白质的大分子进行印迹仍然是挑战。这项研究的目的是通过表面分子印迹技术在MWNT表面上合成Lys-MIP膜,然后从蛋清中选择性地识别和纯化Lys。在最佳条件下,以AAm为功能单体,MBA为交联剂,APS和TEMED为引发剂制备Lys-MIP薄膜。该聚合物也通过TEM,FT-IR,TGA和BET表征。进行了平衡吸附实验和动态吸附实验,以确定结合能力和平衡时间。结果表明,Lys-MIP膜在0.50 mg mL〜(-1)时的吸附容量为20.89 mg g〜(-1),NIP的吸附容量为15.37 mg g〜(-1)。在30分钟内获得82.10%的结合,并在300分钟内达到吸附平衡。选择性吸附实验表明,Lys-MIP膜对Lys的亲和力和容量比对竞争蛋白,如Cyt C,Mb,Hb和BSA的亲和力和容量更高。 Lys / Cyt C,Lys / Mb,Lys / Hb和Lys / BSA的相对选择性系数分别为1.30、1.30、3.12和2.82。从蛋清中纯化Lys的实验表明,Lys-MIP膜的吸附能力是NIP的1.86倍。所有这些结果证明Lys-MIP膜具有高吸附能力和优异的选择性。该材料具有分离真实样品中Lys的巨大潜力。

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