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首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >An integrated electrochemical biosensor based on target-triggered strand displacement amplification and 'four-way' DNA junction towards ultrasensitive detection of PIK3CA gene mutation
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An integrated electrochemical biosensor based on target-triggered strand displacement amplification and 'four-way' DNA junction towards ultrasensitive detection of PIK3CA gene mutation

机译:基于目标触发链位移扩增的集成电化学生物传感器和“四路”DNA结朝着超细敏感性检测PIK3CA基因突变

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摘要

A novel electrochemical biosensor was constructed for specific and ultrasensitive detection of PIK3CA(H1047R) gene mutation based on Nsbl restriction enzyme-mediated strand displacement amplification (NsbI-SDA) and fourway DNA junction for the first time. In this biosensor, the NsbI restriction enzyme combined with strand displacement amplification (SDA) was able to specifically distinguish PIK3CA(H1047R) gene mutation and increase the number of DNA copies to improve electrochemical response. In the presence of target mutation gene, DNA fragments produced by the cleavage event of NsbI restriction enzyme could trigger the SDA reaction to generate massive linker chains. When the linker chains were captured on the electrode, the four-way DNA junction was then attached at the end of linker chain. By integrating electroactive molecules of methylene blue (MB) into four-way DNA junction, this sandwich-like electrochemical biosensor was able to determine the specific distinction of target mutation gene with a low detection limit of 0.001%. Finally, this strategy could be used to analyze mutation gene spiked into human serum samples, indicating the potential application in genetic analysis and clinical disease diagnosis.
机译:基于NSBL限制酶介导的链位移扩增(NSBI-SDA)和第一次,构建了一种新型电化学生物传感器的PIK3CA(H104R)基因突变的特异性和超声检测。在这种生物传感器中,NSBI限制酶与链置换扩增(SDA)结合(SDA)能够特别区分PIK3CA(H1047R)基因突变并增加DNA拷贝的数量以改善电化学反应。在存在靶突变基因的存在下,通过NSBI限制酶的切割事件产生的DNA片段可以引发SDA反应以产生大量的接头链。当将接头链捕获在电极上时,然后在接头链的末端附着四通DNA结。通过将亚甲基蓝(MB)的电活性分子与四元途中的DNA结合,这种类似的电化学电化学生物传感器能够确定目标突变基因的特异性区别,低检测限为0.001%。最后,该策略可用于分析突出的突变基因掺入人血清样本中,表明遗传分析和临床疾病诊断中的潜在应用。

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