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Microcontact printed diaphorase monolayer on glass characterized by atomic force microscopy and scanning electrochemical microscopy

机译:以原子力显微镜和扫描电化学显微镜为特征的玻璃上微接触印刷的心肌黄递酶单层

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Micropatterns of diaphorase (Dp) were fabricated on glass substrates by the microcontact printing (mu CP) method and characterized with atomic force microscopy (AFM) and scanning electrochemical microscopy (SECM). AFM images of the printed samples revealed that the mean height of the Dp patterns was 3-5 nm, indicating the formation of a monolayer pattern. The Dp molecules on the surface organized themselves into two-dimensional arrays. We used two kinds of inking solutions: Dp-phosphate buffer solution (PBS) (pH 7.0) and Dp-PBS (pH 7.0) with glutaraldehyde (GA, 1% v/v) as a cross-linking reagent. Although the AFM imaging showed high-quality Dp monolayer patterns in both cases, SECM measurements indicated that the enzymatic activity of Dp was almost lost when Dp-PBS with GA was used as the inking solution, whereas clear enzymatic activity was found when Dp-PBS was used. (C) 2007 Elsevier B.V. All rights reserved.
机译:通过微接触印刷(mu CP)方法在玻璃基板上制备心肌黄递酶(Dp)的微图案,并通过原子力显微镜(AFM)和扫描电化学显微镜(SECM)对其进行表征。印刷样品的AFM图像表明,Dp图案的平均高度为3-5nm,表明形成了单层图案。表面上的Dp分子将自己组织成二维阵列。我们使用了两种上墨溶液:Dp-磷酸盐缓冲溶液(PBS)(pH 7.0)和Dp-PBS(pH 7.0),戊二醛(GA,1%v / v)作为交联剂。尽管在两种情况下,AFM成像均显示出高质量的Dp单层模式,但SECM测量表明,当将带有GA的Dp-PBS用作上墨溶液时,Dp的酶促活性几乎丧失,而当使用Dp-PBS时,发现了清晰的酶促活性被使用了。 (C)2007 Elsevier B.V.保留所有权利。

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