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首页> 外文期刊>Biochemistry >A piezoelectric quartz crystal biosensor: The use of two single cysteine mutants of the periplasmic Escherichia coli glucose/galactose receptor as target proteins for the detection of glucose
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A piezoelectric quartz crystal biosensor: The use of two single cysteine mutants of the periplasmic Escherichia coli glucose/galactose receptor as target proteins for the detection of glucose

机译:压电石英晶体生物传感器:利用周质大肠杆菌葡萄糖/半乳糖受体的两个单个半胱氨酸突变体作为靶蛋白检测葡萄糖

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摘要

We have examined the potential utility of a glucose biosensor that employs the glucose/galactose receptor of Escherichia coli with a quartz crystal microbalance (QCM). Two different genetically engineered mutant proteins were utilized, each involving, the incorporation of a single cysteine into the amino acid C, sequence of the protein. The proteins were immobilized on the surface of a piezoelectric crystal by a direct sulfur-gold linkage. Since the cysteines were located at different positions in the sequence, the receptors attach to the surface with different orientations. Considering only mass effects, the target sugars for this receptor are predicted to be too small to be detectable with a QCM. However, our sensors indicated measurable and reproducible frequency responses when immobilized receptor was exposed to sugar. This unexpectedly large frequency response occurs because the protein film is transformed from a viscous layer to a more rigid nondissipative film. The QCM can detect these changes because of the direct linkage of the proteins to the surface. Calculations of the frequency response expected for a viscoelastic film with different rheological characteristics support this hypothesis. This study is significant because it illustrates a widened applicability for the QCM methodology to protein systems that bind small molecules and undergo ligand-induced conformational changes.
机译:我们已经检查了葡萄糖生物传感器的潜在效用,该传感器利用大肠杆菌的葡萄糖/半乳糖受体和石英晶体微量天平(QCM)。利用了两种不同的基因工程突变蛋白,每种涉及将单个半胱氨酸掺入该蛋白的氨基酸C序列中。通过直接的硫金键将蛋白质固定在压电晶体的表面上。由于半胱氨酸位于序列中的不同位置,因此受体以不同的方向附着于表面。仅考虑质量效应,预计该受体的目标糖太小而无法用QCM检测到。但是,当固定的受体暴露于糖时,我们的传感器显示出可测量和可再现的频率响应。发生这种意想不到的大频率响应是因为蛋白质膜从粘性层转变为更坚硬的非耗散膜。由于蛋白质与表面的直接连接,QCM可以检测到这些变化。具有不同流变特性的粘弹性薄膜的预期频率响应的计算支持了这一假设。这项研究意义重大,因为它说明了QCM方法对于结合小分子并经历配体诱导的构象变化的蛋白质系统的广泛适用性。

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