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SPR-based single nucleotide mismatch biosensor

机译:基于SPR的单核苷酸错配生物传感器

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The detection and characterization of the hybridization event of 21-base, unlabeled DNA oligonucleotides with a monolayer of complementary DNA immobilized on a gold surface, by electrochemical impedance spectroscopy and surface plasmon resonance (SPR) is presented. A thiol modification on the probe DNA strand allowed for its attachment to the surface viaself-assembly. For the hybridization of full match target DNA a detection limit of 20 pM was determined. RNA hybridization was also detectable with the same sensor, with a similar detection limit. The SPR signal generated upon hybridization of the full match was always distinguishable from the single mismatch target DNA oligonucleotides when the mismatch was in the middle or at the proximal end of the target DNA sequence. However, the response of the sensor was identical for the hybridization of the full match and the distal end mismatch. The SPR sensor described is reusable over at least 20 hybridization/regeneration cycles and is insensitive to flow rate (20–800 μL min?1) or temperature (20–60 °C). Based on the SPR response, the surface density of the probe was estimated to be at least 4.3 × 1012 molecules per cm2...
机译:介绍了通过电化学阻抗谱和表面等离子体共振(SPR)检测并鉴定了21个碱基的未标记DNA寡核苷酸,该寡核苷酸具有固定在金表面的互补DNA单层。探针DNA链上的巯基修饰使其可以通过自组装连接到表面。为了杂交完全匹配的靶DNA,确定了20 pM的检测极限。使用相同的传感器也可以检测到RNA杂交,检测限相似。当错配在靶DNA序列的中间或近端时,在完全匹配的杂交后产生的SPR信号总是与单个错配靶DNA寡核苷酸区分开。但是,对于完全匹配和远端错配的杂交,传感器的响应是相同的。所述的SPR传感器可在至少20个杂交/再生循环中重复使用,并且对流速(20–800μLmin?1)或温度(20–60°C)不敏感。根据SPR响应,探针的表面密度估计至少为每平方厘米4.3×1012分子。

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