Raghava Smita, Mondal Kalyani, Gupta Munishwar N, Pareek Pradeep, Kuckling Dirk
Chemistry Department, Indian Institute of Technology, Delhi, Hauz Khas, New Delhi, India.
Artif Cells Blood Substit Immobil Biotechnol. 2006;34(3):323-36. doi: 10.1080/10731190600683902.
Covalent attachment of enzymes and other proteins to the smart polymer, poly(N-isopropylacrylamide) [poly (NIPAAm)], has been widely used as a method for the preparation of thermosensitive protein conjugates. In the present study, reversible soluble-insoluble polymer-enzyme conjugates were prepared by conjugating a copolymer of NIPAAm with 5-mol % of 6-acrylaminohexanoic acid to trypsin by the carbodiimide-NHS (N-hydroxysuccinimide) coupling method. Four bioconjugates with different units of enzyme coupled to the matrix were prepared. Increased enzymatic activity in terms of high effectiveness factor (in the range of 3-5) was found in the conjugates. Kinetic parameters for the immobilized and free enzyme were determined. The Vmax/Km value of the enzyme significantly increased on immobilization by the factors in the range of 12-28. The immobilized enzyme also showed stability to autolysis at 50 degrees C.
将酶和其他蛋白质共价连接到智能聚合物聚(N-异丙基丙烯酰胺)[聚(NIPAAm)]上,已被广泛用作制备热敏蛋白缀合物的方法。在本研究中,通过碳二亚胺-NHS(N-羟基琥珀酰亚胺)偶联法,将含有5摩尔%6-丙烯酰胺基己酸的NIPAAm共聚物与胰蛋白酶偶联,制备了可逆的可溶-不溶性聚合物-酶缀合物。制备了四种不同酶单位与基质偶联的生物缀合物。在缀合物中发现以高效因子(3-5范围内)表示的酶活性增加。测定了固定化酶和游离酶的动力学参数。固定化后,酶的Vmax/Km值显著增加,增加因子在12-28范围内。固定化酶在50℃下也表现出对自溶的稳定性。