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Graphene-based portable SPR sensor for the detection of Mycobacterium tuberculosis DNA strain

机译:基于石墨烯的便携式SPR传感器,用于检测结核分枝杆菌DNA菌株

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In this study, we presented the novel concept of graphene utilization for the detection of Mycobacterium tuberculosis DNA (deoxyribonucleic acid) hybridization in surface plasmon resonance (SPR) biosensor. The DNA sequences were obtained from DNA fragment IS6110, which was proven as the stable biomarker for Mycobacterium tuberculosis complex (MTBC). A few graphene layers on top of SPR sensing chip were deposited by simple drop casting method from its dispersion solution. The presence of graphene layers plays the major role for single strain DNA immobilization. The single strain DNA (ssDNA) was covalently bond with the gold nano urchin (GNu) as the sensing probe (ssDNA-GNu). The binding mechanism between graphene layers and ssDNA probe is mainly due to the π-π stacking force. Furthermore, hydrogen bond influences the hybridization mechanism of the complementary single strain DNA (cssDNA) and the ssDNA; which has the higher energy compared to the π-π stacking force. Consequently, the presence of the cssDNA target in the reaction chamber disrupts the ssDNA-GNu from the few graphene layers. The experimental results demonstrated the detection limit of this method was achieved around 28 fM of cssDNA target in the salt buffer.
机译:在这项研究中,我们提出的石墨烯利用新颖概念用于检测结核分枝杆菌DNA在表面等离子体共振(SPR)生物传感器(脱氧核糖核酸)的杂交。从DNA片段IS6110获得DNA序列,被证明是结核分枝杆菌复合物(MTBC)的稳定生物标志物。通过从分散溶液中通过简单的液滴铸造方法沉积SPR传感芯片顶部的几个石墨烯层。石墨烯层的存在对单菌株DNA固定化起主要作用。单个菌株DNA(SSDNA)与金纳米核(GNU)共价键合,作为传感探针(SSDNA-GNU)。石墨烯层和SSDNA探针之间的结合机制主要是由于π-π堆叠力。此外,氢键影响互补单菌株DNA(CSSDNA)和SSDNA的杂交机理;与π-π堆叠力相比,这具有较高的能量。因此,反应室中的CSSDNA靶的存在破坏了来自几种石墨烯层的SSDNA-GNU。实验结果表明,在盐缓冲液中达到约28℃的CSSDNA靶标的检测限。

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