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Immunofunctionalisation of gold transducers for bacterial detection by physisorption

机译:金换能器的免疫功能化,用于通过物理吸附进行细菌检测

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Functionalisation of the sensing surface is a key factor in immunosensor fabrication as it allows target-selective capture and prevents nonspecific adsorption of undesired components. Gold immunofunctionalisation using self-assembled monolayers (SAM) has been widely exploited to this end for the detection of small targets. However, we recently demonstrated that this strategy fails when detecting whole bacteria cells (Baldrich et al., Anal Bioanal Chem 390:1557–1562, 2008). We now investigate different physisorption-based alternatives using E. coli as the target organism. Our results demonstrate that physisorption generates the appropriate substrate for the specific detection of bacteria on gold surfaces, providing detection limits down to 105 cells mL?1 in an ELISA-type colorimetric assay. Additionally, surface coverage is highly reproducible when assayed by impedance spectroscopy and the inter- and intra-assay coefficients of variation are below 10–15% in all cases. These surfaces were stable, retained functionality and did not suffer from significant biomolecule desorption after 10 days storage in PBS at 37 °C, hence confirming physisorption as a cheap, simple and efficient strategy for the detection of bacteria.
机译:感测表面的功能化是免疫传感器制造中的关键因素,因为它可以进行靶标选择性捕获,并防止非特异性吸附不需要的成分。为此,使用自组装单分子膜(SAM)进行金免疫功能化已被广泛用于检测小目标。但是,我们最近证明,在检测整个细菌细胞时,这种策略会失败(Baldrich等人,Anal Bioanal Chem 390:1557–1562,2008)。现在,我们研究使用大肠杆菌作为目标生物的不同基于物理吸附的替代方法。我们的结果表明,物理吸附可为金表面细菌的特异性检测提供合适的底物,在ELISA型比色测定法中,检测限可低至105 细胞mL?1 。此外,当通过阻抗光谱法测定时,表面覆盖率具有很高的重现性,并且在所有情况下,测定间和测定内变异系数均低于10-15%。这些表面是稳定的,保留了功能,并且在37°C的PBS中保存10天后,没有明显的生物分子解吸,因此确认了物理吸附是一种廉价,简单且有效的细菌检测策略。

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