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Non-labeled QCM Biosensor for Bacterial Detection using Carbohydrate and Lectin Recognitions

机译:使用碳水化合物和凝集素识别技术进行细菌检测的非标记QCM生物传感器

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摘要

High percentages of harmful microbes or their secreting toxins bind to specific carbohydrate sequences on human cells at the recognition and attachment sites. A number of studies also show that lectins react with specific structures of bacteria and fungi. In this report, we take advantage of the fact that a high percentage of microorganisms have both carbohydrate and lectin binding pockets at their surface. We demonstrate here for the first time that a carbohydrate non-labeled mass sensor in combination with lectin-bacterial O-antigen recognition can be used for detection of high molecular weight bacterial targets with remarkably high sensitivity and specificity. A functional mannose self-assembled monolayer (SAM) in combination with lectin Con A was used as molecular recognition elements for the detection of E. coli W1485 using Quartz Crytsal Microbalance (QCM) as a transducer. The multivalent binding of Concanavalin A (Con A) to the Escherichia coli (E. coli) surface O-antigen favors the strong adhesion of E. coli to mannose modified QCM surface by forming bridges between these two. As a result, the contact area between cell and QCM surface increases that leads to rigid and strong attachment. Therefore it enhances the binding between E. coli and the mannose. Our results show a significant improvement of the sensitivity and specificity of carbohydrate QCM biosensor with a experimental detection limit of a few hundred bacterial cells. The linear range is from 7.5 × 102 to 7.5 × 107 cells/mL that is four decade wider than the mannose alone QCM sensor. The change of damping resistances for E. coli adhesion experiments was no more than 1.4% suggesting that the bacterial attachment was rigid, rather than a viscoelastic behavior. Little non-specific binding was observed for Staphylococcus aureus and other proteins (Fetal Bovine serum, Erythrina cristagalli lectin). Our approach not only overcomes the challenges of applying QCM technology for bacterial detection but also increases the binding of bacteria to their carbohydrate receptor through bacterial surface binding lectins that significantly enhanced specificity and sensitivity of QCM biosensors. Combining carbohydrate and lectin recognition events with an appropriate QCM transducer can yield sensor devices highly suitable for the fast, reversible and straightforward on-line screening and detection of bacteria in food, water, clinical and biodefense areas.
机译:高百分比的有害微生物或其分泌的毒素会在识别和附着位点与人体细胞上的特定碳水化合物序列结合。大量研究还表明,凝集素会与细菌和真菌的特定结构发生反应。在本报告中,我们利用了以下事实:大量微生物在其表面都具有碳水化合物和凝集素结合口袋。我们在这里首次证明,与凝集素细菌O抗原识别相结合的碳水化合物非标记质量传感器可用于检测具有高灵敏度和特异性的高分子量细菌靶标。功能性甘露糖自组装单分子膜(SAM)与凝集素Con A的结合用作分子识别元件,使用Quartz Crytsal Microbalance(QCM)作为传感器来检测大肠杆菌W1485。伴刀豆球蛋白A(Con A)与大肠杆菌(E.coli)表面O-抗原的多价结合通过在两者之间形成桥接而促进了大肠杆菌对甘露糖修饰的QCM表面的强粘附。结果,电池和QCM表面之间的接触面积增加,从而导致牢固牢固的附着。因此,它增强了大肠杆菌和甘露糖之间的结合。我们的结果表明,碳水化合物QCM生物传感器的灵敏度和特异性有了显着提高,实验检测极限为数百个细菌细胞。线性范围为7.5×10 2 至7.5×10 7 细胞/ mL,比单独使用甘露糖的QCM传感器宽四倍。大肠杆菌粘附实验的阻尼阻力变化不超过1.4%,表明细菌附着是刚性的,而不是粘弹性。几乎没有观察到金黄色葡萄球菌和其他蛋白质(胎牛血清,Crerygalli凝集素)的非特异性结合。我们的方法不仅克服了应用QCM技术进行细菌检测的挑战,而且通过细菌表面结合凝集素提高了细菌与其碳水化合物受体的结合,从而显着提高了QCM生物传感器的特异性和敏感性。将碳水化合物和凝集素识别事件与适当的QCM传感器相结合,可以生产出非常适合用于食品,水,临床和生物防御领域中细菌的快速,可逆和直接在线筛选和检测的传感器设备。

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