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Molecularly imprinted polymer anchored on the surface of denatured bovine serum albumin modified CdTe quantum dots as fluorescent artificial receptor for recognition of target protein

机译:molecularly imprinted polymer anchored on the surface of denatured bovine serum albumin modified CdTe quantum dots as fluorescent artificial receptor for recognition of target protein

摘要

A new type of molecularly imprinted polymer (MIP)-based fluorescent artificial receptor was developed by anchoring MIP on the surface of denatured bovine serum albumin (dBSA) modified CdTe quantum dots (QDs) using the surface molecular imprinting process. The approach combined the merits of molecular imprinting technology and the fluorescent property of the CdTe QDs. The dBSA was used not only to modify the surface defects of the CdTe QDs, but also as assistant monomer to create effective recognition sites. Three different proteins, namely lysozyme (Lyz), cytochrome c (Cyt) and methylated bovine serum albumin (mBSA), were tested as the template molecules and then the receptors were synthesized by sol-gel reaction (imprinting process). The results of fluorescence and binding experiments demonstrated the recognition performance of the receptors toward the corresponding template. Under optimum conditions, the linear range for Lyz was from 1.4 x 10(-8) to 8.5 x 10(-6) M, and the detection limit was 6.8 nM. Moreover, the new artificial receptors were applied to separate and detect Lyz in real samples. This fluorescent artificial receptor may serve as a starting point in the design of highly effective synthetic fluorescent receptor for recognition of target protein. (C) 2011 Elsevier B.V. All rights reserved.
机译:通过使用表面分子印迹方法将MIP锚定在变性牛血清白蛋白(dBSA)修饰的CdTe量子点(QDs)表面上,开发了一种新型的基于分子印迹聚合物(MIP)的荧光人工受体。该方法结合了分子印迹技术的优点和CdTe QD的荧光性质。 dBSA不仅用于修饰CdTe QD的表面缺陷,而且还用作辅助单体以创建有效的识别位点。以溶菌酶(Lyz),细胞色素c(Cyt)和甲基化牛血清白蛋白(mBSA)这三种不同的蛋白质为模板分子,然后通过溶胶-凝胶反应(印迹过程)合成受体。荧光和结合实验的结果证明了受体对相应模板的识别性能。在最佳条件下,Lyz的线性范围为1.4 x 10(-8)到8.5 x 10(-6)M,检测极限为6.8 nM。此外,新的人工受体被用于分离和检测真实样品中的Lyz。该荧光人工受体可以用作设计用于识别靶蛋白的高效合成荧光受体的起点。 (C)2011 Elsevier B.V.保留所有权利。

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