Wang Huafang, Li Wenyou, He Xiwen, Chen Langxing, Zhang Yukui
Key Laboratory of Functional Polymer Materials, Ministry of Education of China, Department of Chemistry, Nankai University, Tianjin 300071, China.
React Funct Polym. 2008 Sep 1;68(9):1291-1296. doi: 10.1016/j.reactfunctpolym.2008.06.002.
Using m-aminophenylboronic acid (APBA) as a functional monomer, molecularly imprinted polymer (MIP) imprinted with bovine serum albumin (BSA) was fabricated on activated glass spheres under optimized conditions. Key factors in the prepolymerization reaction (between APBA and BSA), such as buffer pH, ionic strength and reaction time, were carefully optimized as previously reported [1]. The interaction between APBA and BSA during the prepolymerization stage was investigated and optimized, and ideal conditions for protein rebinding experiments were determined as well. Protein rebinding and enriching properties of polymers were studied in single and competitive binding protocols, respectively. The key point of the present paper is that the binding selectivity of polymers may be estimated by the amount of bound-protein recovered from a protein-saturated polymer. Results demonstrated that the selectivity of MIP towards its template protein is superior to that of non-imprinted polymer (NIP).
以间氨基苯硼酸(APBA)为功能单体,在优化条件下于活化玻璃微球上制备了以牛血清白蛋白(BSA)为模板的分子印迹聚合物(MIP)。如先前报道[1]所述,对预聚合反应(APBA与BSA之间)中的关键因素,如缓冲液pH值、离子强度和反应时间进行了仔细优化。研究并优化了预聚合阶段APBA与BSA之间的相互作用,并确定了蛋白质重结合实验的理想条件。分别在单结合和竞争结合方案中研究了聚合物的蛋白质重结合和富集特性。本文的关键点在于,聚合物的结合选择性可通过从蛋白质饱和聚合物中回收的结合蛋白量来评估。结果表明,MIP对其模板蛋白的选择性优于非印迹聚合物(NIP)。