György E, Sima F, Mihailescu I N, Smausz T, Megyeri G, Kékesi R, Hopp B, Zdrentu L, Petrescu S M
Consejo Superior de Investigaciones Cientificas, Instituto de Ciencia de Materiales de Barcelona and Centre d'Investigacions en Nanociència i Nanotecnologia, Campus UAB, 08193 Bellaterra, Spain.
J Biomed Mater Res A. 2009 Apr;89(1):186-91. doi: 10.1002/jbm.a.31963.
Urease thin films have been immobilized using matrix-assisted pulsed laser evaporation for biosensor applications in clinical diagnostics. The targets exposed to laser radiation were made of frozen composites that had been manufactured by dissolving urease in distilled water. An UV KrF* (lambda = 248 nm, tauFWHM congruent with 30 ns, nu = 10 Hz) excimer source was used for the multipulse laser irradiation of the targets that were cooled down to solidification using Peltier elements. The incident laser fluence was set at 0.4 J/cm2. The surface morphology and chemical bonding states of the laser immobilized urease thin films were investigated by atomic force microscopy and Fourier transform infrared spectroscopy. The enzymatic activity and kinetics of the immobilized urease were assayed by the Worthington method, which monitors urea hydrolysis by coupling ammonia production to a glutamate dehydrogenase reaction. Decreased absorbance was found at 340 nm and correlated with the enzymatic activity of urease.
已使用基质辅助脉冲激光蒸发法固定脲酶薄膜,用于临床诊断中的生物传感器应用。暴露于激光辐射的靶材由将脲酶溶解于蒸馏水中制成的冷冻复合物构成。使用紫外KrF*(波长λ = 248 nm,半高宽τFWHM约为30 ns,频率ν = 10 Hz)准分子源对靶材进行多脉冲激光辐照,靶材利用珀耳帖元件冷却至凝固状态。入射激光能量密度设定为0.4 J/cm²。通过原子力显微镜和傅里叶变换红外光谱对激光固定的脲酶薄膜的表面形态和化学键合状态进行了研究。采用沃辛顿法测定固定化脲酶的酶活性和动力学,该方法通过将氨的产生与谷氨酸脱氢酶反应偶联来监测尿素水解。在340 nm处发现吸光度降低,且与脲酶的酶活性相关。