A selective molecularly imprinted polymer for immobilization of acetylcholinesterase (AChE): an active enzyme targeted and efficient method

被引:6
作者
Demirci, Gokhan [1 ]
Dogac, Yasemin Ispirli [2 ]
Teke, Mustafa [2 ]
机构
[1] Marie Curie Sklodowska Univ, Fac Chem, Polymer Chem, PL-20031 Lublin, Poland
[2] Mugla Sitki Kocman Univ, Fac Sci, Dept Chem, Mugla, Turkey
关键词
selective immobilization; molecular recognition; acetylcholinesterase; molecularly imprinted polymer; COLORIMETRIC DETERMINATION; EXTRACTION;
D O I
10.1002/jmr.2475
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In the present study, we immobilized acetylcholinesterase (AChE) enzyme onto acetylcholine removed imprinted polymer and acetylcholine containing polymer. First, the polymers were produced with acetylcholine, substrate of AChE, by dispersion polymerization. Then, the enzyme was immobilized onto the polymers by using two different methods: In the first method (method A), acetylcholine was removed from the polymer, and then AChE was immobilized onto this polymer (acetylcholine removed imprinted polymer). In the second method (method B), AChE was immobilized onto acetylcholine containing polymer by affinity. In method A, enzyme-specific species (binding sites) occurred by removing acetylcholine from the polymer. The immobilized AChE reached 240% relative specific activity comparison with free AChE because the active enzyme molecules bounded onto the polymer. Transmission electron microscopy results were taken before and after immobilization of AChE for the assessment of morphological structure of polymer. Also, the experiments, which include optimum temperature (25-65 degrees C), optimum pH (3-10), thermal stability (4-70 degrees C), kinetic parameters, operational stability and reusability, were performed to determine the characteristic of the immobilized AChE. Copyright (c) 2015 John Wiley & Sons, Ltd.
引用
收藏
页码:645 / 650
页数:6
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